Patent Grant
11591565
The present application relates to stem cell growth media. The present application also relates to media used to induce mature or somatic cells to revert to less mature state.
Stem cell therapy holds the promise of being able to not only treat but cure many acquired diseases, heritable conditions and consequences of traumatic injury. However, there are a number of gaps in current scientific knowledge as well as technical and regulatory barriers that need to be overcome before the promise of stem cell therapies can become reality. The first problem involves regulatory issues. FDA will impose guidelines to ensure patient safety and product reproducibility, which are expected to be modeled after those required for traditional drugs. This would mean that any therapeutic cell that began as a stem cell would need to be generated, from day-1, using defined, quantifiable reagents and under reproducible conditions. In the case of stem cell derived cells for therapy, this has not been possible. Both human embryonic stem (ES) cells as well as human induced pluripotent stem (iPS) cells have traditionally been propagated in vitro using complex mixtures of largely undefined components. Current practice is still to culture ES and iPS cells over a layer of fibroblast feeder cells that are usually of murine origin (mouse embryonic fibroblasts: MEFs) although human feeder cells have also been used. The use of cells from another species is considered by many to be unsafe. In addition to the issue of a different animal species, the requirement for a layer of feeder cells introduces another layer of irreproducibility into the system; the growth of the stem cells requires factors that are secreted by the fibroblast feeder cells. These required factors have not been identified or quantified. In an attempt to get away from the use of feeder cells, stem cells have been grown over a layer of Matrigel, which is a mixture of undefined and unquantifiable factors derived from mouse sarcoma cells. Stem cells can be grown over a layer of Matrigel, however, only if conditioned media from the feeder cells is added. Thus, the Matrigel method does not provide defined conditions for generating cells.
Conventionally known growth factor that enables human stem cell growth is basic fibroblast growth factor (bFGF also called FGF-2, or simply FGF). In an effort to develop stem cell growth conditions that could meet expected FDA regulations for human stem cell therapeutics, a recent research article reported that human embryonic stem cells and iPS cells could be grown using a defined media, called “E8,” which does not contain animal components but that contains extremely high levels of bFGF (100 ng/mL compared to standard 4 ng/mL) plus TGF-beta. The major problem with this media and all other FGF-based media is that true pluripotent stem cells, called “ground” state or “naive” state cells, are unstable in FGF (J. Hanna, A. W. Cheng, K. Saha et al., Proc Natl Acad Sci USA 107 (20), 9222 (2010), Jacob H. Hanna, Krishanu Saha, and Rudolf Jaenisch, Cell 143 (4), 508 (2010), J. Nichols and A. Smith, Cell Stem Cell 4 (6), 487 (2009)). These reports conclude that the use of FGF or bFGF drives human stem cells from the naïve state into a “primed” state. “Primed” is a misnomer. Although primed stem cells have already undergone a degree of differentiation, this does not “prime” them or set them up to differentiate into functional human cells. The opposite is true. Scientific studies now show that primed stem cells are not able to differentiate into any cell in the human body, which is required for the use of stem cells for most if not all therapeutic applications (FGF signaling inhibits neural induction in human embryonic stem cells. Boris Greber, Philippe Coulon, Miao Zhang, Soren Moritz, Stefan Frank, Arnoldo Jose{acute over ( )} Muller-Molina, Marcos J Arauzo-Bravo, Dong Wook Han, Hans-Christian Pape and Hans R Scholer. The EMBO Journal (2011) 30, 4874-4884). For example, FGF grown stem cells can not differentiate into all types of neuronal cells required for treatment for neurodegenerative diseases like Parkinson's or Alzheimer's or for traumatic spinal cord injury. In addition, researchers have not been able to make human stem cells differentiate in a coordinated way, so they randomly differentiate into many cell types whereas for therapeutics, one wants a single type of cell required for that therapy. Researchers do not have these problems when working with mouse stem cells because they are in the naïve state. Another problem with the E8 media is the unusually high levels of bFGF and TGF-beta, which are considered not to be physiologically relevant, and therefore calls into question whether or not these unnaturally high levels of growth factors will cause another unforeseen problem.
In summary, the body of recent research, into differences between primed and naïve or ground state stem cells, concludes that FGF is not the natural growth factor that makes the true pluripotent human stem cells grow. The fact that human stem cells that are in the true pluripotent state (ground state or naive) cannot be maintained in the presence of FGF indicates that there is a need in the art to identify and use the real growth factor that supports the growth of the truly pluripotent human naive stem cells for generating or maintaining human stem cells for human therapeutics. The true growth factor for naïve stem cells should be able to work in a variety of media and culture conditions, including those expected to be required by drug regulatory agencies.
In one aspect, the present invention is directed to a cell culture media for growth, maintenance and induction of reversion to a less mature state of a cell comprising a MUC1* activating ligand. The cell may be stem or progenitor cell in the case where the cell is desired to be proliferated without differentiation occurring, or the cell may be somatic, mature or progenitor cell in which the mature or progenitor cell is desired to be induced to be a pluripotent cell. Preferably, the cell may be human cell. Preferably the media may be free of bFGF, TGF-beta or both. Further, in another aspect, the media may be free of serum. The media may further include insulin, selenium, transferrin, 1-ascorbic acid or non-essential amino acids.
In another aspect, the MUC1* ligand may be an NME family protein. Preferably, the NME family protein may be NME1. The NME1 may exist as two monomers dimerized or engineered as a single chain having two subunits. Alternatively, NME family protein may be NME7 or NME6.
In another aspect, the cell culture media may include an inhibitor of a rho associated kinase. The cell culture media may include an inhibitor of a guanine exchange factor. The inhibitor of the guanine exchange factor may be NME1 in hexamer form or a peptide derived from NME1.
In further other aspect, the cell culture media may further include other growth factors, such as without limitation FGF-2 or TGF-beta.
In another aspect, the invention is directed to a method that includes contacting cells with cell culture media of NME family protein to stimulate growth of stem or progenitor cells or to induce cells to revert to a less mature state.
In this method, the cells may be stem or progenitor cells in the case where the cells are desired to be proliferated without differentiation occurring, or the cells may be somatic, mature or progenitor cells in which the mature or progenitor cells are desired to be induced to be pluripotent. Preferably, the cells may be human cells. Preferably the media may be free of bFGF, TGF-beta or both. Further, in another aspect, the media may be free of serum. The media may further include insulin, selenium, transferrin, 1-ascorbic acid or non-essential amino acids.
Preferably, the NME family protein may be NME1. The NME1 may exist as two monomers dimerized or engineered as a single chain having two subunits. Alternatively, NME family protein may be NME7 or NME6.
In another aspect of the inventive method, the cell culture media may include an inhibitor of a rho associated kinase. The cell culture media may include an inhibitor of a guanine exchange factor. The inhibitor of the guanine exchange factor may be NME1 in hexamer form or a peptide derived from NME1. In further other aspect, the cell culture media may further include other growth factors, such as without limitation FGF-2 or TGF-beta.
In yet another aspect, the invention is directed to a cell culture media of NME family protein, plus a base media and non-essential amino acids for the growth or maintenance of stem cells or induction to pluripotency of mature cells.
In another aspect, the invention is directed to a method that includes contacting cells with cell culture media of NME family protein in serum-free minimal media to stimulate growth of stem or progenitor cells or to induce cells to revert to a less mature state.
In yet another aspect, the invention is directed to a composition that includes a stem cell population, in which the composition further includes a serum-free culture media that includes NME family of proteins.
In yet another aspect, the invention is directed to a method of growing stem cells on a surface on which are ligands that bind to the progenitor or stem cells, comprising contacting the cells with media that includes NME family of proteins.
In another aspect, the present invention is directed to a method of making a pure population of naïve stem cells, comprising: (i) contacting cells with cell culture media comprising NME family protein so as to obtain a single colony of naïve stem cells; (ii) isolating the single colony of naïve stem cells; and (iii) contacting the colony with cell culture media comprising NME family protein to obtain a pure population of naïve stem cells. In step (i) above, about 25 to 60%, or 30 to 50% of the cells in naïve state may be obtained. In the method above, in step (iii), the purity of the population of naïve stem cell may be at least about 80%, 90%, 95%, 99%, or 100%.
In another aspect, the invention is directed to a method of making a pure population of naïve stem cells from induced pluripotent stem cells, comprising: (i) contacting mature or progenitor cells with cell culture media comprising NME family protein so as to obtain a single colony of naïve stem cells; (ii) isolating the single colony of naïve stem cells; and (iii) contacting the colony with cell culture media comprising NME family protein to obtain a pure population of naïve stem cells. The mature cells may be transfected with pluripotency genes in step (i). The mature or progenitor cells may be somatic cells, dermablasts or fibroblasts. In step (i) above, about 25 to 60%, or 30 to 50% of the cells in naïve state may be obtained. In the method above, in step (iii), the purity of the population of naïve stem cell may be at least about 80%, 90%, 95%, 99%, or 100%.
In one aspect, the cell media and the method of using the cell media indicated above may include cell culture media that includes NME7, which has molecular weight of approximately 25 kDa or approximately 30 kDa. The NME7 protein may be NME7-AB. The cell culture media may include an inhibitor of a rho associated kinase, or an activator of signaling proteins in the PI3K or RAC pathway preferably in the absence of a rho kinase inhibitor. Or, the cell culture media may further comprise nucleic acids that suppress expression of NME1 or NME2.
In yet another aspect, the present invention is directed to a method of generating human embryonic stem cell lines comprising: (i) contacting cells derived from a blastocyst with cell culture media comprising NME family protein; (ii) isolating outgrowths having stem-like morphology; (iii) contacting the isolated outgrowths with cell culture media comprising NME family protein; and (iv) and isolating clones that have the desired karyotype and express levels of pluripotency and naïve genes that indicate the cells are pluripotent. In this method, the NME family member may be NME7. The NME7 may be NME7-AB. The media containing the NME family member preferably may not contain FGF. The above method may include the step of suppressing NME1 and NME2 in the cells.
In another aspect, the invention is directed to a method of generating human induced pluripotent stem cell lines comprising: (i) contacting cells derived from a donor or patient with cell culture media comprising NME family protein; (ii) contacting the cells with agents that induce expression of pluripotency genes OCT4, SOX2, NANOG, KLF4, c-Myc or LIN28; (iii) isolating cells having stem cell-like morphology; (iv) contacting the isolated cells with cell culture media comprising NME family protein; (v) isolating clones that have the desired karyotype and express levels of pluripotency genes that indicate the cells are pluripotent; and (vi) and propagating clones in a media comprising an NME family member. In this method, the NME family member may be NME7. The NME7 may be NME7-AB. The media containing the NME family member preferably may not contain FGF. The above method may include the step of suppressing NME1 and NME2 in the cells.
In another aspect, the present invention includes syncing the differentiation time of the stem cells. In particular, the cells may be induced to turn into stem cells, and then at an appropriate point, the cells may be caused to differentiate at the same time.
In yet another aspect, the invention is directed to a stem cell line that has been passaged more than four times, which conventionally has not been done before. Further, the present invention is drawn to a population of naïve cells concentrated so as to be effective.
The present invention will become more fully understood from the detailed description given herein below, and the accompanying drawings which are given by way of illustration only, and thus are not limitative of the present invention, and wherein;
The MUC1* extra cellular domain is defined primarily by the PSMGFR sequence (GTINVHDVETQFNQYKTEAASRYNLTISDVSVSDVPFPFSAQSGA (SEQ ID NO:6)). Because the exact site of MUC1 cleavage depends on the enzyme that clips it, and that the cleavage enzyme varies depending on cell type, tissue type or the time in the evolution of the cell, the exact sequence of the MUC1* extra cellular domain may vary at the N-terminus.
NME family proteins, numbered 1-10, are proteins grouped together because they all have at least one NDPK (nucleotide diphosphate kinase) domain. In some cases, the NDPK domain is not functional in terms of being able to catalyze the conversion of ATP to ADP. NME proteins were formally known as NM23 proteins, numbered H1, H2 and so on. Herein, the terms NM23 and NME are interchangeable. Herein, terms NME1, NME2, NME6 and NME7 are used to refer to the native protein as well as NME variants. In some cases these variants are more soluble, express better in E. coli or are more soluble than the native sequence protein. For example, NME7 as used in the specification can mean the native protein or a variant, such as NME7-AB that has superior commercial applicability because variations allow high yield expression of the soluble, properly folded protein in E. coli. “NME1” as referred to herein is interchangeable with “NM23-H1”. It is also intended that the invention not be limited by the exact sequence of the NME proteins. The mutant NME1-S120G, also called NM23-S120G, are used interchangeably throughout the application. The S120G mutants and the P96S mutant are preferred because of their preference for dimer formation, but may be referred to herein as NM23 dimers or NME1 dimers.
NME7 as referred to herein is intended to mean native NME7, or variants that increase yield, solubility or other characteristics that make the NME7 more effective or commercially more viable.
As used herein, FGF, FGF-2 or bFGF refer to fibroblast growth factor.
As used herein, Rho associated kinase inhibitors may be small molecules, peptides or proteins (Rath N, Olson M F. Rho-associated kinases in tumorigenesis: re-considering ROCK inhibition for cancer therapy. EMBO Rep. 2012; 13(10):900-8). Examples of rho kinase inhibitors are Y27632, HA-1077, also called Fasudil, H-1152 and thiazovivin (Olson M F. Applications for ROCK kinase inhibition. Curr Opin Cell Biol. 2008; 20(2):242-8; Watanabe K, Ueno M, Kamiya D, et al. A ROCK inhibitor permits survival of dissociated human embryonic stem cells. Nat Biotechnol. 2007; 25(6):681-6; Breitenlechner C, Gassel M, Hidaka H, et al. Protein kinase A in complex with Rho-kinase inhibitors Y-27632, Fasudil, and H-1152P: structural basis of selectivity. Structure. 2003; 11(12):1595-607; Lin T, Ambasudhan R, Yuan X, et al. A chemical platform for improved induction of human iPSCs. Nat Methods. 2009; 6(11):805-8). In addition to Rho kinase inhibitors, the invention envisions using inhibitors of related pathways in place of the Rho kinase inhibitors. For example, in the same pathway, guanine exchange factors (GEFs) are upstream of Rho kinase. The GEFs activate the Rho kinases. Therefore, instead of using rho kinase inhibitors, the invention envisions using GEF inhibitors. Since rho kinase is in the inactive state when bound to GDP, any agent that increases the amount of GDP present in a cell, such as RAD, GEM, and RhoE as well as others, can be used in place of rho kinase inhibitors to aid in stem cell growth, survival and attachment to surfaces (Riento K, Guasch R M, Garg R, Jin B, Ridley A J (2003) RhoE binds to ROCKI and inhibits downstream signaling. Mol Cell Biol 23: 4219-4229; Komander D, Garg R, Wan P T, Ridley A J, Barford D (2008) Mechanism of multi-site phosphorylation from a ROCK-I:RhoE complex structure. EMBO J 27: 3175-3185; Ward Y, Yap S F, Ravichandran V, Matsumura F, Ito M, Spinelli B, Kelly K (2002) The GTP binding proteins Gem and Rad are negative regulators of the Rho-Rho kinase pathway. J Cell Biol 157: 291-302), in their place. Myosin is also in the same pathway as Rho kinases. Myosin is indirectly activated by Rho kinase and as such is downstream of rho kinase in the same pathway. Therefore, myosin inhibitors can also be used in place of rho kinase inhibitors according to methods of the invention to aid in stem cell survival and/or to aid in stem cell attachment to surfaces. Blebbistatin is a myosin inhibitor and can be used in place of any rho kinase inhibitor used according to methods of the invention (Ohgushi M, Matsumura M, Eiraku M, Murakami K, Aramaki T, Nishiyama A, et al. Molecular pathway and cell state responsible for dissociation-induced apoptosis in human pluripotent stem cells. Cell Stem Cell 2010; 7:225-39; Ohata H, Ishiguro T, Aihara Y, et al. Induction of the Stem-like Cell Regulator CD44 by Rho Kinase Inhibition Contributes to the Maintenance of Colon Cancer-Initiating Cells. Cancer Res. 2012; 72(19):5101-10).
Rho kinase inhibitors are abbreviated here and elsewhere as ROCi or ROCKi. The use of specific rho kinase inhibitors are meant to be exemplary and can be substituted for any other rho kinase inhibitor.
Sequence Listing Free Text
As regards the use of nucleotide symbols other than a, g, c, t, they follow the convention set forth in WIPO Standard ST.25, Appendix 2, Table 1, wherein k represents t or g; n represents a, c, t or g; m represents a or c; r represents a or g; s represents c or g; w represents a or t and y represents c or t.
describes full-length MUC1 Receptor (Mucin 1 precursor, Genbank Accession number: P15941).
SEQ ID NOS:2, 3 and 4 describe N-terminal MUC-1 signaling sequence for directing MUC1 receptor and truncated isoforms to cell membrane surface. Up to 3 amino acid residues may be absent at C-terminal end as indicated by variants in SEQ ID NOS:2, 3 and 4.
describes a truncated MUC1 receptor isoform having nat-PSMGFR at its N-terminus and including the transmembrane and cytoplasmic sequences of a full-length MUC1 receptor.
describes Native Primary Sequence of the MUC1 Growth Factor Receptor (nat-PSMGFR—an example of “PSMGFR”):
describes Native Primary Sequence of the MUC1 Growth Factor Receptor (nat-PSMGFR—An example of “PSMGFR”), having a single amino acid deletion at the N-terminus of SEQ ID NO:6).
describes “SPY” functional variant of the native Primary Sequence of the MUC1 Growth Factor Receptor having enhanced stability (var-PSMGFR—An example of “PSMGFR”).
describes “SPY” functional variant of the native Primary Sequence of the MUC1 Growth Factor Receptor having enhanced stability (var-PSMGFR—An example of “PSMGFR”), having a single amino acid deletion at the C-terminus of SEQ ID NO:8).
describes MUC1 cytoplasmic domain nucleotide sequence.
describes MUC 1 cytoplasmic domain amino acid sequence.
describes NME7 nucleotide sequence (NME7: GENBANK ACCESSION AB209049).
describes NME7 amino acid sequence (NME7: GENBANK ACCESSION AB209049).
describes NM23-H1 nucleotide sequence (NM23-H1: GENBANK ACCESSION AF487339).
describes amino acid sequence (NM23-H1: GENBANK ACCESSION AF487339).
describes NM23-H1 S120G mutant nucleotide sequence (NM23-H1: GENBANK ACCESSION AF487339).
describes NM23-H1 S120G mutant amino acid sequence (NM23-H1: GENBANK ACCESSION AF487339).
describes NM23-H2 nucleotide sequence (NM23-H2: GENBANK ACCESSION AK313448).
describes NM23-H2 amino acid sequence (NM23-H2: GENBANK ACCESSION AK313448).
Human NM23-H7-2 Sequence Optimized for E. coli Expression:
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Human NME7-A:
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Human NME7-A1:
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Human NME7-A2:
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Human NME7-A3:
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Human NME7-B:
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Human NME7-B1:
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Human NME7-B2:
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Human NME7-B3:
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Human NME7-AB:
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Human NME7-AB 1:
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Human NME7-A Sequence Optimized for E. coli Expression:
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Human NME7-A1 Sequence Optimized for E. coli Expression:
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Human NME7-A2 Sequence Optimized for E. coli Expression:
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Human NME7-A3 Sequence Optimized for E. coli Expression:
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Human NME7-B Sequence Optimized for E. coli Expression:
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Human NME7-B1 Sequence Optimized for E. coli Expression:
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Human NME7-B2 Sequence Optimized for E. coli Expression:
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Human NME7-B3 Sequence Optimized for E. coli Expression:
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Human NME7-AB Sequence Optimized for E. coli Expression:
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Human NME7-AB 1 Sequence Optimized for E. coli Expression:
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Mouse NME6
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Human NME6:
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Human NME6 1:
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Human NME6 2:
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Human NME6 3:
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Human NME6 Sequence Optimized for E. coli Expression:
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Human NME6 1 Sequence Optimized for E. coli Expression:
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Human NME6 2 Sequence Optimized for E. coli Expression:
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Human NME6 3 Sequence Optimized for E. coli Expression:
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OriGene-NME7-1 Full Length
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Abnova NME7-1 Full Length (Amino Acids)
NME6 S139G (Human)
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NME6 HutoS (Human)
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NME-6 S139G Sequence Optimized for E. coli Expression
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NME-6 HutoS Sequence Optimized for E. coli Expression
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Abnova Partial NME7-B
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Histidine Tag
(ctcgag)caccaccaccaccaccactga (SEQ ID NO:84)
Strept II Tag
Ligands of MUC1*
The inventors previously disclosed that ligands of the MUC1* receptor can function as growth factors, and in particular are growth factors for stem and progenitor cells. NME family proteins (previously called NM23) are ligands of MUC1*. NME proteins are grouped together because they all have an NDPK (nucleotide diphosphate kinase) domain. NME1 or NME2 expressed or purified such that a significant population exists as a dimer, support the growth of embryonic or induced pluripotent stem cells in the absence of feeder cells, their extracts, serum or any other cytokine. Herein, we report that NME7 is also a ligand of MUC1* and also supports the growth of embryonic or induced pluripotent stem cells in the absence of feeder cells, their extracts, serum or any other cytokine. NME6, NME1 and NME2 all have a single NDPK domain and are of similar molecular weight. NME7 is twice their molecular weight and contains two NDPK domains. NME6 can exist as a dimer, like NME1. Therefore, NME1, NME2 and NME6 in dimeric form and NME7 are preferred NME family proteins for the growth of stem or progenitor cells, which included but are not limited to mesenchymal stem cells, hematopoietic stem cells, pluripotent stem cells and naïve state stem cells, as well as for the maintenance or induction of pluripotency. Especially preferred are NME1 and NME7. Still more preferred are NME1 in dimeric form and NME7. It is not intended that the invention be restricted to the natural forms of the proteins. For commercial advantage, the proteins may be made as recombinant proteins that may bear mutations, truncations or additional sequences. Herein, this NME7 variant is referred to simply as NME7 since the invention is not meant to be limited by specific variants that may increase the yield of expressed recombinant protein, solubility and the like. Further, the invention envisions the use of single chain variants of NME1 or NME6, wherein the single chain protein is comprised of two connected monomers, wherein each monomer may consist of a single NDPK A or B domain.
Induced Pluripotency
Forced expression of combinations of the transcription factors, Oct4, Sox2, Klf4 and c-Myc or Oct4, Sox2, Nanog and Lin28 have been shown to cause mature cells to revert to the pluripotent state (Takahashi and Yamanaka, 2006). Each of the transcription factors that induce pluripotency regulates the transcription of about a dozen genes. Among these were several that the inventor has identified as being MUC1-associated factors. OCT4 and SOX2 bind to the MUC1 promoter itself. Pluripotency proteins SOX2 and NANOG bind to the NME7 promoter, underscoring its importance for pluripotency of stem cells. NM23 (also known as NME) was previously identified, by the present inventor, as the activating ligand of MUC1* (Mahanta et al., 2008). NME7 is an activating ligand of MUC1*. OCT4 and SOX2 both bind to the promoter for MMP16 which we disclose herein is a cleavage enzyme of MUC1. OCT4, SOX2 or NANOG also bind to promoter sites for cleavage enzymes MMP2, MMP9, MMP10, ADAM TSL-1, ADAM TS-4, ADAM-17 (a MUC1 cleavage enzyme), ADAM-TS16, ADAM-19 and ADAM-28. Some or all of these cleavage enzymes may be upregulated to enhance the cleavage of MUC 1 to the MUC1* form to induce pluripotency or maintain it (Boyer et al, 2005). Taken together, it is clear that MUC1* (cleaved form) and its ligand NME7 are activators of pluripotency, since the key pluripotency proteins, SOX2 and NANOG bind to the NME7 promoter and OCT4 and SOX2 bind to the MUC1 promoter, and turn on expression of these genes.
Our previous work with embryonic stem cells, which only express the cleaved form of MUC1, MUC1*, showed that dimerization of its extracellular domain stimulate growth and inhibit differentiation (Hikita et al., 2008). These effects were achieved by dimerizing the MUC1* extracellular domain using either a bivalent Anti-MUC1* antibody (
Surface Plasmon Resonance (SPR) experiments were performed that show that only NME1 dimers bind to the MUC1* extra cellular domain peptide.
These findings indicate that MUC1* is a significant “stemness” factor. In addition, OCT4 and SOX2 bind to the MUC1 gene promoter and also to the promoter of its cleavage enzymes. SOX2 and NANOG bind to the NM23 (NME7) promoter. Since blocking the extracellular domain of MUC1* is lethal to hES cells, it follows that the pluripotency genes, OCT4, SOX2, and NANOG, bind to the promoter sites of MUC1, its cleavage enzymes and its activating ligand NME7 and induce their expression of MUC1. One or more of the genes or gene products that have already been shown to induce pluripotency can be replaced by transfecting the gene or introducing the gene product for MUC1* alone or in addition to its cleavage enzymes and/or activating ligands, NME7, NME-H1, NME-H2 or an antibody that dimerizes the PSMGFR epitope of MUC1 or MUC1*.
Experiments were performed to test the efficiency of induction of pluripotency in somatic cells using the standard protocol that uses FGF-based media or an altered protocol that uses NME-based media.
The conventionally used standard protocol is to first plate dermablasts or fibroblasts (human foreskin fibroblast-neonatal, “hFFn”: #PC501A-hFF, System Biosciences, Mountain View, Calif.) on plastic and culture them in fibroblast media (FM), changed every 24 hours. After 5 days, the cells are transferred to a surface coated with inactivated fibroblast feeder cells, which can be mouse (MEFs) or human (HS27). For the next 2 days, cells remain in FM. On Day 7 the media is changed to bFGF-based media and media is changed every 24 hours. ˜2-4 weeks post initial plating, colonies (clones) that have embryonic stem (ES) cell-like morphology are selected and individually plated into new wells coated with inactivated feeder cells (MEFs or HS27s) and sequentially passaged every 3-4 days. Wells that continue to grow as ES-like cells are propagated and tested for the presence of pluripotency markers.
Contrary to the conventionally used standard protocol, we cultured the somatic cells in NME media always (NME1 dimers: “NM23-MM-A”). In addition, we either plated the cells over a layer of fibroblast feeder cells or over a layer of anti-MUC1* antibody (C3 or C8 that recognize the N-10 PSMGFR peptide. RT-PCR measurements were performed to quantify the amount of Oct4 expressed under a variety of conditions by Day 4 (
In a preferred embodiment, NM23 (NM23-H1, NM23-H2, or NME7) is introduced to cells, as the gene that encodes it, as the protein itself or as a protein bearing a leader sequence such as a poly-arginine tract, to facilitate entry into the cell, to aid in the induction or maintenance of pluripotency. The inventors recently showed that when NM23 is secreted by pluripotent stem cells (and cancer cells), it is an activating ligand of the cleaved form of MUC1-MUC1*—and triggers the MAP kinase proliferation pathway. NM23 stimulation of MUC1* was shown to promote the growth of pluripotent hESCs and inhibited their differentiation (Hikita et al., 2008). NM23 also induces the transcription of c-MYC (Dexheimer at al., 2009) and replaces the need for c-MYC. NM23 is added exogenously either in its native state to activate the MUC1* growth factor receptor or with a poly arginine tract to facilitate entry into the cell and nucleus where it induces C-MYC expression. NM23 (NME) may be added as the encoding nucleic acid, or as the expressed protein with or without a modification that facilitates entry into the cell. NME1 or NME2 can be used in their native state or in mutant forms that favor the dimeric state, such as the S120G mutation or NME7.
In another aspect of the invention, a bivalent antibody that binds to the extracellular domain of MUC1* (PSMGFR) or a dimeric MUC1* ligand, such as NM23, or genes encoding them are added to MUC1*-expressing cells to induce pluripotency, increase the efficiency of the induction of pluripotency, to maintain pluripotency or to inhibit differentiation. The cells to which these MUC 1 or MUC1* interacting proteins are added may be naturally occurring cells or those into which genes to induce stem cell-like characteristics have been added, or have already entered the differentiation process or may be stem cells.
Genes for inducing pluripotency may be introduced on the same or different plasmids, which may be lenti viral vector driven or adenovirus vectors or any integrating or non-integrating viral or non-viral vector, or any other system that facilitates introduction of these genes into the desired cells.
In many cases, it is preferential to achieve the effects of pluripotency-inducing proteins by introducing the proteins themselves rather than the nucleic acids or genes that encode them. The invention encompasses genes disclosed here for the induction of stem-like characteristics or pluripotency that can be replaced by the gene products, the proteins, either in their native state or modified with leader sequences such as poly-arginine tracts to allow entry into the cells. The products of these genes, i.e. proteins, or other proteins which interact with one or more of the products of the transfected genes are introduced to cells to induce or maintain pluripotency or other stem-cell like characteristics.
NM23 protein such as, but not limited to, NME-H1, NME-H2, NME6 or NME-7 enhances the induction or maintenance of pluripotency. NM23 is introduced along with one or more of the previously identified pluripotency factors, including but not limited to OCT4, SOX2, KLF4, as well as others disclosed herein.
NM23 Family Proteins
NM23 exists as a family of proteins wherein the commonality among these proteins is the presence of a nucleoside diphosphate kinase (NDPK) domain that catalyzes the conversion of ATP to ADP. NM23 has previously been known as Tumor Metastasis Factor. With the recent identification of ten NM23 family members, they are now also known as NME proteins 1-10 (Boissan et al., Mol Cell Biochem (2009) 329:51-62, “The mammalian Nm23/NDPK family: from metastasis control to cilia movement,”).
Scientists first isolated a differentiation inhibition factor from human leukemia cells and showed that the addition of this factor blocked chemically induced differentiation of certain types of leukemia and myeloid cells (Okabe-Kado, 1985, Cancer Research 45, 4848-4852, “Characterization of a Differentiation-inhibitory Activity from Nondifferentiating Mouse Myeloid Leukemia Cells); this inhibitory factor was later identified as NME1 (NM23-H1) (Okabe-Kado, 1992, “Identity of a differentiation inhibiting factor for mouse myeloid leukemia cells with NM23/nucleoside diphosphate kinase”, Biochem Biophys Res Comm, 182 No. 3 987-994). Leukemia cells are blood cells that are blocked from terminal differentiation. Interestingly, the ability to inhibit differentiation of leukemia cells was shown to be independent of its catalytic domain. Mutations in the NDPK domain that abrogated its enzymatic activity had no effect on the protein's ability to block differentiation of some types of leukemia cells. However, the scientific literature of the following decades paints a picture of total confusion as to whether NM23 inhibits differentiation, accelerates differentiation or has no effect at all.
Many research articles provided evidence indicating that NM23 induces differentiation. Rosengard et al, 1989, Dearolf et al 1993, and Timmons et al 1993 reported that in vivo the Drosophila NM23 homologue, awd, is required for proper differentiation. Lakso et al 1992 reported that NM23 (mouse in vivo) increases with initiation of tissue differentiation, implying that it induces differentiation. Yamashiro et al 1994 reported that in vitro NM23 levels increase during differentiation of human erythroleukemia cells. Lombardi et al 1995 concluded that NM23 (mouse in vitro) increases with initiation of cellular differentiation, again indicating that NM23 induces differentiation. Gervasi 1996, reported that overexpression of NM23 (rat in vitro) induced neuronal differentiation and down regulation of NM23 with anti-sense DNA inhibited differentiation. Amendola et al 1997 showed that transfection of NM23 in human neuroblastoma cells increased differentiation.
In direct contradiction to the many research articles that reported that NM23 induced differentiation, an equal number of papers published in the same time frame reported the opposite: that NM23 inhibited differentiation. Munoz-Dorado et al 1990 found that ndk (Myxococcus NM23 homologue, in vivo) was essential for growth but was down regulated during development, implying that its presence would inhibit differentiation. Okabe-Kado 1992 showed that in vitro a differentiation inhibitory factor (later identified by same group as NM23) inhibited differentiation of mouse leukemia. Yamashiro et al 1994 reported that NM23 levels decrease during differentiation of human megakaryoblasts, consistent with NM23 inhibiting differentiation. Okabe-Kado 1995 showed that recombinant NM23 inhibited erythroid differentiation of leukemia cell lines HEL, KU812, and K562 but not monocyte or granulocyte differentiation of progenitors HL60, U937, or HEL/S cells. Venturelli et al 1995 reported that NM23 overexpression inhibited G-CSF dependent granulocyte differentiation of human hematopoietic progenitors. Willems et al 1998 found that NM23 expression decreases as human CD34+ hematopoietic progenitors from the bone marrow cells differentiate. In 2002, Willems et al showed that NM23 had no effect on cell proliferation, did not induce or inhibit differentiation but skewed differentiation of CD34+ cells toward the erythroid lineage.
In a 2000 review article, Lombardi summarized these and other contradictory results pertaining to the role of NM23 in differentiation and concluded, “Although the role of the NM23 genes in the control of cell differentiation is widely under investigation, the functional connection between NM23 expression levels and such processes remains to be completely elucidated.” In other words, the functional connection between NM23 and differentiation was not understood.
The inventors previously discovered that the growth factor receptor function of a MUC 1 cleavage product, MUC1*, is activated by ligand induced dimerization of its extra cellular domain and that the ligand of MUC1* was NM23. The inventors further demonstrated that it was the dimer form of NM23 that inhibits differentiation and supports the growth of stem and progenitor cells. In addition, the inventors discovered that NM23 species induce pluripotency. We have now discovered that several NM23 family members have this stem-related function. NME1 (NM23-H1) promotes stem cell growth and inhibits differentiation when it is a dimer only. NME6 is roughly the same molecular weight as NME1 and in sea sponge (Suberites domuncula) it is reported to exist as a dimer (Perina et al, 2011, “Characterization of Nme6-like gene/protein from marine sponge Suberites domuncula” Naunyn-Schmiedeberg's Arch Pharmacol, 384:451-460). Although NME7 (NM23-H7) is a monomeric protein, the inventors have discovered that it functions like a dimer. It contains two NDPK catalytic domains, is approximately twice the molecular weight of an NME1 or NME6 monomer and is expressed and secreted by human embryonic stem (ES) and induced pluripotent stem (iPS) cells (see
NME7 can also exist as a smaller protein of molecular weight ˜25 kDa. Pull down assays of stem cell lysates and supernatants were performed followed by mass spectrometry. The smaller molecular weight forms of NME7 all contained peptide sequences from its NDPK A domain, but not from the B domain. This may be an alternative splice isoform or a cleavage product. Like NME1, this smaller A domain NME7 may dimerize.
NME family proteins are differentially expressed at different times of cell and tissue development. Whereas we detect NME6, NME7 and NME1 in embryonic stem cells, only NME1 and NME2 are routinely expressed in adult cells or adult stem cells. Because NME1 forms hexamers which induce rather than inhibit stem cell differentiation, it follows that NME6 and NME7 are expressed earlier in embryogenesis and in true pluripotent stem cells because they cannot form the hexamers.
In the earliest stages of embryogenesis, growth and inhibition of differentiation would be the default, with the regulatory function of the hexamer being important in later stages when one wants to initiate differentiation when a certain density of stem cells is reached. In support of our findings, Boyer et al (Boyer et al, 2005, “Core Transcriptional Regulatory Circuitry in Human Embryonic Stem Cells”, Cell, Vol. 122, 947-956) reported that pluripotency inducing proteins SOX2 and NANOG bind to the promoter of NME7 but not other NME family members, indicating that it is the first NME protein expressed and is consistent with the notion that it can induce or maintain pluripotency but cannot form the hexamers that turn it off. Boyer et al also report that pluripotency inducing proteins SOX2 and OCT4 bind to the promoter of MUC1, the target receptor of NME7 following cleavage to MUC1*. SOX2 and OCT4 also bind to the promoter of the MUC1 cleavage enzyme MMP-16. The fact that these pluripotency inducing proteins redundantly bind to the promoters of MUC1, its cleavage enzyme and its ligand, NME7 argue that this subset of proteins is important to pluripotency and that NME7 is the first of the pluripotency proteins expressed in the developing embryo. NME7 is highly expressed by human stem cells if they are cultured in NM23 variants that prefer dimer formation.
Example 7 describes an experiment in which BGO1v human embryonic stem cells are grown in either NM23-S120G, which has been refolded and purified to exist primarily as a dimer (
Jaenisch and colleagues reported a set of markers of the naïve state and a second set of markers that are characteristic of the primed state (J. Hanna, A. W. Cheng, K. Saha et al., Proc Natl Acad Sci USA 107 (20), 9222 (2010), Jacob H. Hanna, Krishanu Saha, and Rudolf Jaenisch, Cell 143 (4), 508 (2010)). Experiments were performed in which human embryonic stem (ES) or induced pluripotent stem (iPS) cells were cultured in NME1 dimers or in NME7 in a variety of minimal media or they were cultured in FGF-based media. The surfaces upon which the stem cells were plated was also varied. RT-PCR measurements were then performed to measure expression levels of the naïve genes versus the primed genes for cells cultured in NME-based media compared to FGF-based media. In all cases, NME-based media generated stem cells that were in a more naïve state than cells cultured in FGF-based media. For example, cells grown in FGF in minimal media (MM) grown over MEF feeder cells had higher expression of the primed markers and lower expression of the naïve markers than the same source cells grown in NME1 dimers in minimal media (MM) wherein cells were plated over plasticware coated with an anti-MUC1* antibody. Another FGF-based media called mTeSR fared even worse with very high levels of the primed genes and lower levels of the naïve ones (
NME7 exists as a single protein but structurally is comprised of two monomers and so functions as a dimer. NME7 contains two NDPK domains, portions of which bind to the MUC1* growth factor receptor. Example 7 also describes a binding experiment called a pull-down assay. In this experiment, the MUC1* extra cellular domain peptide was attached to beads which were then incubated with lysates from BGO1v human embryonic stem cells. After wash steps and release from the beads, species capture by interaction with the MUC1* peptide were separated on an SDS-PAGE gel then probed with an anti-NME7 antibody.
NME6 exists as a dimer, and resists formation of higher order multimers. NME6 dimers bind to MUC1* growth factor receptor and dimerize it which activates pathways that maintain pluripotency, induce pluripotency and inhibit differentiation of stem and progenitor cells. Like NME1 mutants and variants that prefer dimer formation, both NME6 and NME7 are capable of maintaining and inducing pluripotency and inhibiting differentiation of stem and progenitor cells, including iPS cells.
Like NME1 mutants and variants that prefer dimer formation, NME6 and NME7 can be added exogenously to stem cells (embryonic or induced pluripotent) or progenitor cells to induce growth, maintain them in an undifferentiated state or inhibit their differentiation. NME6 and NME7 can be added exogenously to stem or progenitor cells to induce pluripotency. In addition, nucleic acids encoding NME1 mutants and variants that prefer dimer formation, NME6 and/or NME7, or variants thereof, including single chain variants that behave as dimers, can be introduced into cells to induce the cells to revert to a less differentiated state or to maintain cells in a less mature state.
Because NME is highly conserved among all species, the methods described herein are not intended to be limited to human NME species nor limited to use with human cells.
In another aspect of the invention, we have discovered that the addition of exogenous NME7 fully maintains stem cell growth and pluripotency, inhibits differentiation and is also able to induce pluripotency. NME7 is a monomeric protein that has two NDPK domains, A and B. Until now, its function has not been elucidated. It was previously only known that NME7 was expressed in testes, ovary and brain. NME7 is suspected to be involved in the motility of flagella and is thought not to have NDPK activity because of the lack of certain key residues.
NME7 expressed in E. coli and secreted as a soluble protein was added to human stem cells in culture in a minimal stem cell media devoid of any other growth factor, feeder cells or their conditioned media. The stem cells were adsorbed onto the cell culture plate by adhering to a layer of an antibody that recognizes a stem cell surface antigen. In this way, interference by growth factors and other cytokines present in surface coatings such as Matrigel were avoided.
As a comparison, stem cells from the same source were cultured side-by-side but instead of adding exogenous recombinant NME7, recombinant NM23-H1 (also known as NME1) that had been refolded and purified as a population of dimers was added (See Examples 9 and 10 and
To aid in protein expression and purification, several NME7 constructs were made and tested. Although it has been previously reported that NME7 can be expressed in in vitro expression systems using wheat germ cell extracts (MW 36.52 kDa) and in human HEK293 cells (MW 38 kDa), we found that a smaller construct containing essentially just the NDPK A and B domains can be expressed in E. coli as a soluble protein with very high yields. We made NME7-AB with either a histidine tag or a strep tag, however it can be made without an affinity tag or with any other affinity tag. NME7-AB promoted pluripotency and inhibited differentiation of human stem cells as well as or better than NME1 (NM23-H1) dimers that had previously been shown by us to fully support stem cell growth, maintenance of pluripotency, able to induce pluripotency and inhibit differentiation. Our experiments show that NME7 can substitute for NME1 dimers without the threat of hexamer formation over time and in a more cost-effective and commercially applicable way.
NME family proteins are highly conserved across all species, including plants. Therefore, sequences of NME family members, isoforms and variants of the invention, especially NME1, NME6 and NME7 constructs, may be comprised of sequences from any species or combinations of sequences from different species, with mammalian species being preferred, mouse species still more preferred, and human species most preferred. Such NME family members, isoforms and variants can be used for the propagation of, self-renewal, maintenance of pluripotency, induction of pluripotency or inhibition of differentiation in any species, wherein mammalian species are preferred, mouse species more preferred and human species most preferred.
NME1 in dimeric form or NME7 can also be used for the maintenance of naïve human stem cells or for the induction of naïve stem cells from stem cells in the primed state or for making naïve stem cells from somatic cells in the process of generating iPS cells. Stem cells in the naïve state are characterized by high expression levels of the pluripotency genes OCT4, KLF2 and NANOG or KLF4 and low expression levels of FOXa2, OTX, LHX and XIST compared to stem cells grown in bFGF-containing media. An even more stringent indicator of the naïve state is that the cells have not yet undergone X-inactivation. High levels of XIST are indicators of inactivation of one of the X chromosomes, but a more definite determinant is immunocytochemical staining of Histone 3. If X-inactivation has occurred, Histone 3 is condensed and can be visualized as a discrete mass in the cell's nucleus. If X has not yet been inactivated, Histone 3 is either undetected or is dispersed throughout the nucleus, sometimes referred to as a “cloud.”
Both embryonic stem cells (ES) and induced pluripotent stem (iPS) cells, cultured in NME1 dimers or in NME7 gave rise to stem cells that had reduced levels of FOXa2, OTX, LHX and XIST, compared to cells cultured in FGF and also did not have detectable or condensed Histone 3 in the nucleus of ˜50% of the cells, after at least 8-10 passages in the NME-based media. Cells cultured in NME-based media for 6 passages had only 25% of the cells that were pre-X-inactivation, which is a hallmark of the naïve state. Researchers (J. Hanna, A. W. Cheng, K. Saha et al., Proc Natl Acad Sci USA 107 (20), 9222 (2010), Jacob H. Hanna, Krishanu Saha, and Rudolf Jaenisch, Cell 143 (4), 508 (2010)) who were able to temporarily revert primed stem cells to a naïve state by treating the cells with a variety of biochemicals and inhibitors in addition to ectopically expressing genes, reported about 1 in 10,000 cells were in a naïve state. By using single cell cloning techniques they were able to isolate pure populations of naïve human stem cells, but they were unstable and could only be maintained in the naïve state for a few passages, which was less than 5 passages in most cases. Another indicator of stem cells being in the naïve state is that the cells have a higher cloning efficiency, which is calculated as the number of discrete colonies that can be counted per a specified number of cells plated. The cloning efficiency of mouse stem cells, which unlike human stem cells, are easily maintained in the naïve state by culturing in media containing mLIF (murine leukemia inducing factor), is ˜30%. By stark contrast, the cloning efficiency of human stem cells cultured in FGF-based media is ˜1%. ES cells cultured in NME1 dimers had a cloning efficiency of 18% and the same cells cultured in NME7 had a cloning efficiency of 23%. However, these were cell populations that only had about 50% of the cells in the naïve state by Histone-3 staining. Therefore, the actual cloning efficiency of the naïve cells in that population is at least 2-times the measured 20%, which is about 40% cloning efficiency which is above that of mouse naïve stem cells. Taken together, these data show that stem cells cultured in NME1 or NME7 revert from the primed state to a naïve state and are maintained in a naïve state.
The invention also envisions the use of NME1 or NME7 to generate populations of stem cells that are essentially 100% pluripotent and in the naïve state. By merely culturing currently commercially available ES or iPS cells in media containing NME1 dimers or NME7, populations of cells are generated that are about 50% in the completely naïve state. Using cloning techniques, known to those skilled in the art, such as limiting dilution, on mixed population of naïve and primed stem cells, populations of stem cells that are all in the naïve state are generated. In yet another aspect of the invention new stem cell lines are generated. ES cell lines are generated using previously described techniques (Embryonic Stem Cell Lines Derived from Human Blastocysts. James A. Thomson, Joseph Itskovitz-Eldor, Sander S. Shapiro, Michelle A. Waknitz, Jennifer J. Swiergiel, Vivienne S. Marshall, Jeffrey M. Jones et al. Science 282, 1145 (1998); DOI: 10.1126/science.282.5391.1145; Isolation of Embryonic Stem (ES) Cells in Media Supplemented with Recombinant Leukemia Inhibitory Factor (LIF). Shirley Pease, Paola Braghetta, J David Gearing, Dianne Grail, and R. Lindsay Williams Developmental Biology 141, 344-352 (1990)) with the exception that instead of culturing cells in FGF, which drives the naturally naïve cells into the primed state, cells are cultured in media containing NME7 or NME1 wherein at least some of the NME1 protein is in the dimeric state, more preferably wherein at least 25% of the protein is in the dimeric state and still more preferably wherein at least 50% of the protein is a dimer. In one aspect, cells are derived from the inner cell mass of a human blastcyst and cultured in a media containing NME7 or NME1 dimers. In another aspect of the invention, somatic cells, such as dermablasts or fibroblasts are induced to revert to a less mature state by culturing in a media containing NME7 or NME1 dimers. In yet another aspect of the invention, iPS cell lines are generated by transducing somatic cells, dermablasts or fibroblasts with one or more of the pluripotency genes Oct4, Sox2, Klf4, Nanog, c-Myc, or LIN28 or by treating the cells with the products of those genes, i.e., the proteins or with agents that cause the proteins to be produced and doing so in the presence of a media that contains NME1 dimers or NME7. More generally, the invention envisions generating new iPS cell lines, which are produced with greater efficiency or are in a more naïve state than iPS cells generated by traditional methods that include the use of FGF, using any method that induces a cell to revert to a less mature state, including a pluripotent state, by culturing the cells in the presence of NME1 dimers or NME7. In a preferred embodiment, the use of FGF is eliminated. In another preferred embodiment, cells undergoing the process of generating iPS cells are not transferred onto fibroblast feeder cells.
Surfaces for Growing Stem Cells
It is not intended that the invention be limited by the nature of the surface upon which the stem cells or the cells undergoing induction of pluripotency are grown. Any suitable surface for stem cell growth or induction of pluripotency can be used with media containing NME1, NME6, or NME7. Such surfaces include but are not limited to feeder cells, Matrigel, hydrogels, integrins and integrin derivatives, E-cadherin and E-cadherin derivatives, vitronectin, antibodies to cell surface receptors, antibodies that recognize the MUC1* extra cellular domain, antibodies that recognize the PSMGFR sequence, Vita™ brand plates (ThermoFisher), VITA™ plates coated with an anti-MUC1* antibody and the like. NME1 mutants and variants that can form stable dimers (P96S, S120G mutants and a single chain construct) were added to minimal stem cell media (MM) and used to propagate stem cells that were growing over a Matrigel surface or an anti-MUC1* antibody coated surface. The growth of the stem cells and their ability to resist spontaneous differentiation was essentially equal in all three media and on both surfaces (
In some cases, a rho kinase inhibitor is used to enhance adhesion of the cells to the surface. Many rho kinase inhibitors, including but not limited to HA100, Y27632, and thiozivincan be used to aid in enhancing adhesion of stem cells to surfaces, particularly to the surfaces that are plastic coated with anti-MUC1* antibodies. For most stem cell lines currently available, a rho kinase inhibitor is added for the first 24-48 hours only.
Alternatively, inhibitors of guanine exchange factors (GEFs) are added to the media instead of rho kinase inhibitor for at least a portion of the culture period, to enhance adhesion to surfaces that are not cells or comprised of complex cell mixtures such as Matrigel Inhibitors of GEFs are used in some cases instead of rho kinase inhibitors to enhance the attachment of stem cells to surfaces that are coated with anti-MUC1* antibodies. In one aspect of the invention, the guanine exchange factor inhibitor is NME1 in hexameric form. In another aspect of the invention, the guanine exchange factor inhibitor is a peptide that is derived from NME1.
Inhibitors of rho kinase or guanine exchange factor may be required for maximal adhesion of primed stem cells or mixed populations of primed and naïve stem cells to certain surfaces, such as plates coated with anti-MUC1* antibodies. However, pure populations of naïve stem cells do not require the use of rho kinase inhibitors or guanine exchange factor inhibitors. In one aspect of the invention, pure populations of naïve stem cells are cultured in the absence of FGF or a rho kinase inhibitor.
Rho kinase inhibitors are agents that inhibit rho kinase I or II. They may be small molecules, peptides or proteins Rath N, Olson M F. Rho-associated kinases in tumorigenesis: re-considering ROCK inhibition for cancer therapy. EMBO Rep. 2012; 13(10):900-8. Examples of rho kinase inhibitors are Y27632, HA-1077, also called Fasudil, H-1152, and thiazovivin (Olson M F. Applications for ROCK kinase inhibition. Curr Opin Cell Biol. 2008; 20(2):242-8; Watanabe K, Ueno M, Kamiya D, et al. A ROCK inhibitor permits survival of dissociated human embryonic stem cells. Nat Biotechnol. 2007; 25(6):681-6; Breitenlechner C, Gassel M, Hidaka H, et al. Protein kinase A in complex with Rho-kinase inhibitors Y-27632, Fasudil, and H-1152P: structural basis of selectivity. Structure. 2003; 11(12):1595-607; Lin T, Ambasudhan R, Yuan X, et al. A chemical platform for improved induction of human iPSCs. Nat Methods. 2009; 6(11):805-8). In addition to Rho kinase inhibitors, the invention envisions using inhibitors of related pathways in place of the Rho kinase inhibitors. For example, in the same pathway, guanine exchange factors (GEFs) are upstream of Rho kinase. The GEFs activate the Rho kinases. Therefore instead of using rho kinase inhibitors, the invention envisions using GEF inhibitors. Since rho kinase is in the inactive state when bound to GDP, any agent that increases the amount of GDP present in a cell, such as RAD, GEM, and RhoE as well as others, can be used in place of rho kinase inhibitors to aid in stem cell growth, survival and attachment to surfaces (Riento K, Guasch R M, Garg R, Jin B, Ridley A J (2003) RhoE binds to ROCKI and inhibits downstream signaling. Mol Cell Biol 23: 4219-4229; Komander D, Garg R, Wan P T, Ridley A J, Barford D (2008) Mechanism of multi-site phosphorylation from a ROCK-I:RhoE complex structure. EMBO J 27: 3175-3185; Ward Y, Yap S F, Ravichandran V, Matsumura F, Ito M, Spinelli B, Kelly K (2002) The GTP binding proteins Gem and Rad are negative regulators of the Rho-Rho kinase pathway. J Cell Biol 157: 291-302), in their place. Myosin is also in the same pathway as Rho kinases. Myosin is indirectly activated by Rho kinase and as such is downstream of rho kinase in the same pathway. Therefore, myosin inhibitors can also be used in place of rho kinase inhibitors according to methods of the invention to aid in stem cell survival and/or to aid in stem cell attachment to surfaces. Blebbistatin is a myosin inhibitor and can be used in place of any rho kinase inhibitor used according to methods of the invention (Ohgushi M, Matsumura M, Eiraku M, Murakami K, Aramaki T, Nishiyama A, et al. Molecular pathway and cell state responsible for dissociation-induced apoptosis in human pluripotent stem cells. Cell Stem Cell 2010; 7:225-39; Ohata H, Ishiguro T, Aihara Y, et al. Induction of the Stem-like Cell Regulator CD44 by Rho Kinase Inhibition Contributes to the Maintenance of Colon Cancer-Initiating Cells. Cancer Res. 2012; 72(19):5101-10). Another alternative to using a rho associated kinase inhibitor, is to activate or inhibit any target that results in increased cell migration. Activation of modulators of the RAC pathway, that increases cell migration include PI3K, CDC42, PAK, N-WASP as well as RAC1, and lamellipodium. Agents that enhance their expression levels in the cell or increase their activity are used to enhance stem cell survival and attachment to surfaces. RAC1 GTPase expression decreases as stem cells dissociate and conversely Rho associated kinases increase, which leads to loss of cell migration and apoptosis (Ohgushi M, Matsumura M, Eiraku M, et al. Molecular pathway and cell state responsible for dissociation-induced apoptosis in human pluripotent stem cells. Cell Stem Cell. 2010; 7(2):225-39.) Therefore inhibitors of the PI3k or RAC pathway should be suppressed, or activators of RAC pathway increased in order to enhance stem cell survival and attachment to surfaces, such as to antibody coatings wherein the antibody binds to a stem cell surface protein, such as MUC1*. NME1 in hexamer form and NME2, likely also in hexamer form, bind to GEF Tiam1 and Dbl-1 to inhibit GTPases RAC1 and CDC42 GTPase, respectively ((Ohgushi M, Matsumura M, Eiraku M, et al. Molecular pathway and cell state responsible for dissociation-induced apoptosis in human pluripotent stem cells. Cell Stem Cell. 2010; 7(2):225-39; Murakami M, Meneses P I, Knight J S, Lan K, Kaul R, Verma S C, Robertson ES. Nm23-H1 modulates the activity of the guanine exchange factor Dbl-1. Int J Cancer. 2008; 123:500-10; Miyamoto M, Iwashita S, Yamaguchi S, Ono Y. Role of nm23 in the regulation of cell shape and migration via Rho family GTPase signals. Mol Cell Biochem. 2009; 329:175-9). Therefore, inhibition of RAC and CDC42 modulated by NME1 and NME2 hexamers decrease cell migration and limit stem cell attachment and survival. We have suppressed NME1 and NME2 in embryonic and induced pluripotent stem cells in culture in NME7 media and observe no ill effects. Suppression of NME1 and NME2 in stem and progenitor cells that are cultured in NME6 or NME7 containing media are preferred methods for enhancing stem and progenitor cell survival and attachment to surfaces for in vitro culture. In a preferred embodiment, embryonic stem cells or iPS cells are cultured in a media that contains NME7 and siRNA to suppress NME1 and NME2. In a preferred embodiment the nucleic acids that suppress NME1 and NME2 are siRNA molecules derivatized with cholesterol moieties to enable entry into the cells (Darmicon). In a more preferred embodiment the stem cells are not contacted with a rho kinase (ROCK1) inhibitor such as Y27632.
Alternatively, stem cells cultured in media containing NME1, NME6 or NME7, are grown in suspension. A number of techniques for cell growth in suspension are known to those skilled in the art. Wave bags, roller bottles, and the like can be used in association with NME-containing media for stem cell growth or for the induction of pluripotency in more mature cells such as somatic cells, dermablast or fibroblasts. In a preferred embodiment, the NME protein is NME1 in dimer form. In a still more preferred embodiment the NME protein is NME7.
It is not intended that the invention be limited by the nature of the media to which NME1, NME6 or NME7 is added. NME family proteins can be added to any media suitable for stem or progenitor cell growth or any media suitable for the induction of pluripotency. A base media such as DMEM, DMEM/F12, or similar further containing knockout serum replacement or similar and non-essential amino acids are preferred. In a preferred embodiment, the base media contains 60-80% DMEM-like base and 20-40% knockout serum replacement or similar, plus concentrated non-essential amino acids. In other cases the base media contains a DMEM-like base plus insulin, selenium, and transferrin. In cases where the resultant cells are destined for use in a human, the preferred species of the protein components is human.
Ligands of the MUC1* growth factor receptor, in particular NME family proteins, promote the growth of, and maintenance of pluripotency of stem and progenitor cells. MUC1* ligands in a media also support the process of making induced pluripotent stem (iPS) cells and support the process of inducing cells to revert to a less mature state. In addition, MUC1* ligands themselves induce cells to revert to a less mature state in the absence of other factors such as transfection or transduction of pluripotency genes including OCT4, SOX2, KLF4, NANOG or c-Myc.
The inventors previously disclosed that ligands of the MUC1* receptor can function as growth factors. Ligands that dimerize the MUC1* extra cellular domain were shown to increase the growth of MUC1-positive cancer cells and also stem and progenitor cells that expressed MUC1*. The present application discloses that NME7 is also a ligand of the MUC1* growth factor receptor. NME7 is secreted by stem cells. NME7 in a base media devoid of any other cytokines fully supports the growth of embryonic or induced pluripotent stem cells. NME7 functions to promote growth of and maintain pluripotency of stem cells in a manner very similar to NME1 dimers. NME1, expressed or purified such that a significant population exists as a dimer, fully supports the growth of embryonic or induced pluripotent stem cells and does not require serum or any other cytokines. NME1 in dimeric form and NME7 also induce pluripotency in cells that are in a more mature state than the naïve or ground state stem cells. Whereas growth of human stem cells in FGF containing media produce stem cells in the “primed” state, growth of human stem cells in NME1 dimers or NME7 induces those cells to revert to an earlier state called the “naive” or “ground” state. Recent research provides evidence that stem cells in the primed state cannot develop into all the cell types in the human body the way that naïve stem cells can. Therefore, stem cells cultured in NME1 or NME7 that are in a more naïve state are ideally suited for use in human therapies because the naïve state is the natural state of human stem cells and it is those naïve stem cells that are able to develop into any cell in the human body. In a preferred embodiment, stem cells cultured in NME1 or NME7 are used for any and all human stem cell therapies.
The present application discloses that NM23 as a component of a defined, xeno-free media supports stem cell growth, including both embryonic and induced pluripotent and further can be used as the media in which to reprogram somatic, progenitor, or somewhat mature cells such that they become pluripotent stem cells, which are also referred to as iPS cells.
The addition of NM23 to base media DMEM/F12 (or similar) plus insulin (human preferred), selenium, transferrin, 1-ascorbic acid, with pH adjusted using NaHCO3 fully supported ES and iPS cell growth when cells were attached to Vitronectin-coated surfaces or anti-MUC1* coated surfaces. The use of Rho kinase inhibitors HA100 or Y27632 for at least the first 24 hours greatly improved stem cell surface attachment. Especially preferred are NM23 and NM23 variants that can be expressed and/or isolated as dimers. Other growth factors such as FGF-2 or TGF-beta may optionally be added to NM23 in this media. In addition, cells may be grown under hypoxic conditions for improved performance.
The addition of NM23 to base media DMEM/F12 (or similar) plus insulin (human preferred), selenium, transferrin, 1-ascorbic acid, with pH adjusted using NaHCO3 fully supported ES and iPS cell growth when cells were attached to Vitronectin-coated surfaces, anti-MUC1* coated surfaces, Matrigel and other surfaces to which stem cells attach. The use of Rho kinase inhibitors HA100 or Y27632 for at least the first 24 hours greatly improved stem cell surface attachment. Addition of any Rho kinase inhibitor (ROCKi) changes cell shape and attachment properties and can be used in media containing NM23 to enhance the attachment of stem cells, progenitor cells and other non-adherent cells to surfaces. In the presence of a rho kinase inhibitor, cells transition within 24 to 48 hours from a rounded shape with weak surface attachments to a more flattened shape with many surface attachments. Although the use of Rho kinase inhibitors has been previously described for use with stem cells to enhance survival, Rho kinase inhibitors do not increase survival in NME based media. For that reason, it is only used to make cells flatten out and form greater attachments to surface.
The use of rho kinase inhibitors have been previously described for use with bFGF-based media, also to increase survival. Herein, we describe the use of Rho kinase inhibitors to aid in attachment to surfaces when NME1, NME6 or NME7 are used in a media. Especially preferred are NM23 and NM23 variants that can be expressed and/or isolated as dimers as well as NME7, which is a monomer that has two NDPK domains. Although these NDPK domains until now have only been known to have enzymatic activity, the inventors have discovered that a portion of the NDPK domain contains a motif that binds to the MUC1* extra cellular domain.
We have also shown that NME7 functions similarly to NME1 dimers in their ability to support pluripotent stem cell growth and inhibit differentiation. NME7 via NDPK domains, binds to the MUC1* receptor's extra cellular domain to promote pluripotent, naïve stem cell growth and inhibits differentiation. In particular, NME7 binds to the PSMGFR peptide which is a part of the MUC1* extra cellular domain.
NM23-H1, which is also known as NME1, is active as it is a stem or progenitor cell growth factor only when in dimer form. NME1 can exist as a dimer, tetramer or hexamer as a function of concentration as well as its sequence. Mutations such as the S120G or P96S with or without C-terminus deletions prefer dimer formation and are somewhat resistant to hexamer formation so are preferred as stem or progenitor cell growth factors. NME6 exists as a dimer and is also preferred for use as a growth factor, like NME1 dimers, for the maintenance and induction of pluripotency and for inhibition of differentiation. NME7 is a monomer but may bind like a dimer with its two NDPK domains. In pull-down assays NME7 binds to MUC1* extra cellular domain peptide, indicating that portions of at least one NDPK domain binds to the MUC1* receptor, and like NME1 dimers, results in the maintenance or induction of pluripotency while inhibiting differentiation. In a sandwich assay, NME7 was shown to simultaneously bind to two MUC1* extra cellular domain peptides (PSMGFR), indicating that the NME7-AB protein can dimerize MUC1* on the cell surface. NME1 also binds to the MUC1* extra cellular domain peptide and the MUC1* receptor on cells. NME1 hexamers do not bind to the MUC1* receptor and do not maintain or induce pluripotency. NME1 dimers, NME6 dimers, or NME7 for the growth, maintenance, induction of pluripotency and inhibition of differentiation can be used in many different base media that are suitable for culture of stem or progenitor cells. The composition of compatible base media can vary. In some cases, other growth factors or cytokines may be added into the media along with NME protein. Other growth factors such as FGF-2 or TGF-beta may optionally be added to NM23 in this media. In a most preferred embodiment, NME1 dimers, NME6 dimers or NME7 is added to a base media that does not contain other growth factors or cytokines. Cells may be grown under hypoxic conditions for improved performance.
The methods of the invention can act to provide the cells with a growth factor to stimulate the proliferation of a specific population of cells, which may carry a genetic mutation or correction. In one embodiment, an NME family protein is encoded in a nucleic acid sequence that may be contained within a plasmid that is introduced into a cell. The nucleic acid sequence that encodes the NME family protein can be part of a plasmid, or expression vector that also carries the sequence of a gene whose expression is desirable. The gene may be a corrected gene or gene to be expressed. The invention also envisions introducing a nucleic acid encoding an NME family member into a stem cell such that the cell constitutively expresses its own growth factor, simplifying culturing because it would only require a minimal solution for growth. In a preferred embodiment, the nucleic acid is an expression plasmid, which may have an inducible or controllable promoter. In a preferred embodiment the NME family member is NME1, NME6 or NME7. In a still more preferred embodiment the NME family member is NME7. In the most preferred embodiment, the NME family is NME7-AB. The invention also includes the use of these methods, in patients, in cells destined for transplant in patients, in blastocysts and embryos as well as in fertilized or unfertilized eggs, which may be used for in vitro fertilization.
The invention additionally envisions the use of NME-based media for the generation of new stem cell lines that may be embryonic in origin or induced from more mature cells. In a preferred embodiment, the NME-based media is a minimal media containing recombinant NME7. Yet more preferred is a media containing NME7-AB.
New stem cell lines are established as follows: Human cells are harvested from the inner mass of a blastocyst or the entire blastocyst can be used. The cells of the blastocyst are maintained and cultured in a media containing NME7. In a preferred embodiment, the media is free of other growth factors or cytokines. The harvested cells may be plated over a layer of feeder cells, which may be fibroblasts or may be MUC 1-positive cancer cells, or over an antibody layer. In a preferred embodiment, the antibody is an anti-MUC1* antibody. Still more preferred is an antibody that binds to the N-10 PSMGFR peptide. Alternatively the cells may be cultured or maintained in suspension in an NME7 containing media. A variety of techniques known to those skilled in the art can then be used to isolate stem-like cells, which can then be cloned to obtain clones that have the desired karyotype, and the desired gene expression profile. In a preferred embodiment, clones are isolated and proliferated that have gene expression indicative of the naïve state and not the primed state and further have not undergone X-inactivation if the cells are female. In a typical stem cell derivation method, the blastocyst or cells from the blastocyst are plated onto a surface and cultured for some period of time until blast outgrowths are observed that appear stem-like. These are harvested, grown and clones having the desired characteristics are isolated and maintained. Standard cloning techniques are performed to isolate clones that are positive for pluripotency markers as well as naïve markers and having low or no expression of primed markers such as FOXA2, OTX, LHX or sometimes XIST or lack of condensed Histone-3 in the nucleus. Clones are maintained and propagated in minimal media containing NME7 and optionally maintained in the naïve state by growing the cells over a layer of anti-MUC1* antibodies. In an alternative method, the cells are cultured in suspension. A Rho kinase inhibitor may be added to the NME7 containing media. In a preferred embodiment, the media is free of FGF.
It has been demonstrated, in mouse and human, that somatic cells can be reprogrammed by ectopic expression of transcription factors (Lowry et al., 2008; Maherali et al., 2007; Nakagawa et al., 2008; Okita et al., 2007; Park et al., 2008; Takahashi et al., 2006; Takahashi and Yamanaka, 2006; Wernig et al., 2007; Yu et al., 2006) to become pluripotent. The generation of induced pluripotent stem (iPS) cells holds great promise for the realization of truly personalized regenerative medicine (Yamanaka, 2007; Jaenish and Young, 2008) because stem cells derived from a patient's own skin cell can be used to generate cells and tissues to repair damage caused by disease or aging. Forced expression of combinations of the transcription factors, Oct4, Sox2, Klf4 and c-Myc or Oct4, Sox2, Nanog and Lin28 have been shown to cause mature cells to revert to the pluripotent state. However, these methods use FGF-based media throughout the process, which likely slows or corrupts the process of iPS generation.
An improvement over the known technique is to generated iPS cell lines as follows: Somatic cells, dermablasts or fibroblasts which may be from a donor or a patient are cultured in a media containing an NME family protein. In a preferred embodiment the NME family protein is NME1 dimer, NME6, or NME7. In a more preferred embodiment, the NME family member is NME7, wherein NME7-AB is especially preferred. The cells can be treated with nucleic acids, small molecules, or proteins that result in an increase in levels of pluripotency genes or proteins in the cells, wherein the pluripotency genes or gene products are chosen from OCT4, NANOG, KLF4, c-Myc, LIN28, and NME7. In a preferred embodiment, the starting cells are transfected with Oct4, SOX2 and Klf4. The starting cells that are somatic cells, dermablasts, fibroblasts or other cell are initially plated onto plastic multi-well plates in a minimal media containing roughly 2-50 nM NME7, more preferred is 8-16 nM. Media is changed every 24-72 hours as is typical. As cells begin to lose their adhesion to the plastic, they can be moved to a surface to which they will adhere, such as a surface of inactivated fibroblasts, inactivated cancer cells or a surface coated with an antibody to a stem cell surface protein, wherein an anti-MUC1* antibody is preferred. A rho kinase inhibitor may be added to the media in addition to the NME family member. After approximately 2-3 weeks, stem-like cells will have emerged and can be isolated and cloned. Clones with desired karyotype and gene expression profiles are selected and proliferated as stable self-renewing cell lines. In a preferred embodiment, clones that are naïve are selected. Human cells are preferred for these methods of generating new stem cell lines.
It is not intended that the invention be limited by the type of stem or progenitor cell for which the methods of the invention are useful. Essentially any stem or progenitor cells that expresses the cleaved for of MUC1, i.e. MUC1* can be used along with media and methods of the invention.
For a variety of reasons, including FDA compliance, totally defined and xeno-free media are desirable for the growth of human stem cells destined for therapeutic uses. The examples and figures herein demonstrate that NME1 dimers and NME7 fully support pluripotent, naïve stem cell growth and inhibit differentiation and these functions are independent of base media components. Virtually any base media that is suitable for stem cell growth will suffice. Preferred are base media that do not contain other growth factors or cytokines.
Researchers recently reported a base media, called E8, that includes DMEM/F12, insulin, selenium, transferrin, 1-ascorbic acid, and NaHCO3 for pH adjustment, plus bFGF and TGF-beta as the growth factors, which is a defined and xeno-free media for human stem cell growth (Chen G, Gulbranson D, Hou Z et al, “Chemically defined conditions for human iPSC derivation and culture” Nature Methods, Vol. 8. No. 5, 2011 pgs 424-431). This base media, devoid of bFGF and TGF-beta, but with NME1 or NME6 dimers or NME7, that we called “MN6”, was shown to fully support human and mouse pluripotent stem cell growth, inhibited differentiation and also supported the induction of pluripotency during iPS generation. NME1 or NME6 dimers, or NME7 in MN2 media which is a base media and non-essential amino acids only (see Example 1), somewhat supported pluripotent stem cell growth. These findings underscore the fact that NME1 dimers and NME7 are the natural growth factors of human stem cells and can be used in a variety of media suitable for stem or progenitor cell growth. Similar to the E8 media, media suitable for use with NME1 dimers and NME7 is comprised of a base media such as DMEM/F12 or DME/F12/Glutamax I, L-ascorbic acid, sodium selenium, insulin, transferrin and an agent to adjust pH such as sodium bicarbonate. In another aspect of the invention, the base media to which NME1 dimers or NME7 is added is comprised of DME/F12/Glutamax I, a serum replacement such as Knockout serum replacement (LifeTechnologies/Invitrogen), amino acids, such as non-essential amino acid solution (LifeTechnologies/Invitrogen), and optionally beta-mercaptoethanol. Media containing components from each of these base media are also envisioned. In fact, any base media suitable for stem or progenitor cell growth can be used with NME1 dimers and NME7 for the growth of stem or progenitor cells, to inhibit differentiation even to the primed state, and to induce pluripotency in more mature cells, which may be somatic cells, dermablasts, fibroblasts or progenitor cells.
A variety of media supported stem cell growth and inhibited differentiation when mixed with NME1 dimers or NME7. The concentration of NME1 dimers, NME6 dimers, or NME7 can vary. In one aspect the NME concentration is between 1 nM and 100 nM (based on the molecular weight of the monomer). In a preferred embodiment, the concentration of NME1 dimers, NME6 dimers, or NME7 is from 2 nM to 64 nM. In a still more preferred embodiment, the concentration of NME1 dimers, NME6 dimers, or NME7 is 4 nM to 32 nM.
One media called Minimal Media “MM” that when mixed with NME1 dimers or NME7, at 8 nM-16 nM, fully supported human stem cell growth and mouse stem cell growth and made human primed stem cells revert to the naïve state was comprised of:
400 ml DME/F12/GlutaMAX I (Invitrogen #10565-018),
100 ml Knockout Serum Replacement (KO-SR, Invitrogen #10828-028),
5 ml 100× MEM Non-essential Amino Acid Solution (Invitrogen #11140-050), and
0.9 ml (0.1 mM) β-mercaptoethanol (55 mM stock, Invitrogen #21985-023).
Another media that worked similarly when NME1 dimers or NME7 was added at 8 nM-16 nM was “MN6”, comprised of:
DMEM/F12,
L-Ascorbic acid 64 mg/L,
Sodium selenium 14 ug/L,
Insulin 19.4 mg/L,
Sodium Bicarb 543 mg/L, and
Transferrin 10.7 mg/L
Another media that was tested with NME1 dimers or NME7 was added at 8 nM-16 nM was “MN2” comprised of:
400 ml DME/F12/GlutaMAX I (Invitrogen #10565-018), and
5 ml 100×MEM Non-essential Amino Acid Solution (Invitrogen #11140-050)
NME1 dimers and NME7 in “MM” or “MN6” support human stem cell growth as well as or better than the FGF-containing media “E8” or mTeSR. The experiments shown in
In addition to using NM23 in this defined and xeno free media for the growth and maintenance of ES and iPS cells, it is also used in the process of making iPS cells from progenitors or mature somatic cells such as dermablasts.
Cell Culture Media
Any cell culture may be used so long as a MUC1* ligand is either added to the media or is expressed by the cell. In particular, minimal media is preferred that includes MUC1* ligand such as NM23 family of proteins added to the media or expressed by the cell. A minimal media was made that included only DMEM/F12, insulin (human preferred), selenium, transferrin, 1-ascorbic acid, with pH adjusted using NaHCO3 was made; we called this media “MN6”, see detailed formula below. Another minimal media was made that included only 400 ml DME/F12/GlutaMAX I (Invitrogen #10565-018) and 5 ml 100×MEM Non-essential Amino Acid Solution (Invitrogen #11140-050); we called this media MN2, see detailed formula below. NME7, NME6 or NME1 (NM23-S120G) in Another base media called minimal stem cell media or “MM” is comprised of MN2 media plus 100 ml Knockout Serum Replacement (KO-SR, Invitrogen #10828-028) and 0.9 ml (0.1 mM) β-mercaptoethanol (55 mM stock, Invitrogen #21985-023). To these three base media were added 8 nM-16 nM NME7, NME6 or NME1 (NM23-S120G), wherein NME1 was refolded and purified such that the population was essentially all dimers. In some cases a Rho kinase inhibitor (ROCi) such as Y27632 was added. The presence of NME1, NME6 or NME7 in any of these media, promoted pluripotent stem cell growth and inhibited differentiation.
A previously reported media of MN6 plus FGF-2 and TGF-beta, “E8” (G. Chen, D. R. Gulbranson, Z. Hou et al., Nat Methods 8 (5), 424 (2011)), plus/minus Y27632, was compared to NME-based media. In addition, as another control, FGF-2 (also called bFGF) plus 50% MEF conditioned media was used as the media.
The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and accompanying figures. Such modifications are intended to fall within the scope of the appended claims. The following examples are offered by way of illustration of the present invention, and not by way of limitation.
400 ml DME/F12/GlutaMAX I (Invitrogen #10565-018)
100 ml Knockout Serum Replacement (KO-SR, Invitrogen #10828-028)
5 ml 100×MEM Non-essential Amino Acid Solution (Invitrogen #11140-050)
0.9 ml (0.1 mM) β-mercaptoethanol (55 mM stock, Invitrogen #21985-023)
DMEM/F12
L-Ascorbic acid 64 mg/L
Sodium selenium 14 ug/L
Insulin 19.4 mg/L
Sodium Bicarb 543 mg/L
Transferrin 10.7 mg/L
TGFbeta 1 2 ug/L
FGF2 100 ug/L
DMEM/F12
L-Ascorbic acid 64 mg/L
Sodium selenium 14 ug/L
Insulin 19.4 mg/L
Sodium Bicarb 543 mg/L
Transferrin 10.7 mg/L
400 ml DME/F12/GlutaMAX I (Invitrogen #10565-018)
5 ml 100×MEM Non-essential Amino Acid Solution (Invitrogen #11140-050)
Examples 1-3 and
Human ES cells (H9s) were plated onto either a layer of Vitronectin or a layer of anti-MUC1* antibody (MN-C3) on 6-well cell culture plates. For each condition, a Rho kinase inhibitor, Y27632, was present or absent. The presence of the Rho kinase inhibitor for at least the first 24 hours improved cell attachment and performance but was not absolutely essential for undifferentiated stem cell growth.
The results were that NM23 in the dimer form fully supported pluripotent stem cell growth in the 6-component defined and xeno-free media as well as the controls and as well as or better than the combination of FGF-2 and TGF-beta.
In addition to the NM23-S120G refolded and purified as dimers, a single chain NM23 construct that included two NM23 monomer sub-units connected by a flexible linker of G4S1 repeated 2-times—NM23-GS2 and a single chain NM23 construct that included 2 NM23 monomers connected by a longer linker—NM23-X4 were tested and performed as well as the naturally dimerized NM23-S120G.
The conventionally used standard protocol is to first plate dermablasts or fibroblasts (human foreskin fibroblast-neonatal, “hFFn”: #PC501A-hFF, System Biosciences, Mountain View, Calif.) on plastic and culture them in fibroblast media (FM), changed every 24 hours. After 5 days, the cells are transferred to a surface coated with inactivated fibroblast feeder cells, which can be mouse (MEFs) or human (HS27). For the next 2 days, cells remain in FM. On Day 7 the media is changed to bFGF-based media and media is changed every 24 hours. ˜2-4 weeks post initial plating, colonies (clones) that have embryonic stem (ES) cell-like morphology are selected and individually plated into new wells coated with inactivated feeder cells (MEFs or HS27s) and sequentially passaged every 3-4 days. Wells that continue to grow as ES-like cells are propagated and tested for the presence of pluripotency markers.
Contrary to the conventionally used standard protocol, we cultured the somatic cells in NME media always (NME1 dimers: “NM23-MM-A”). In addition, we either plated the cells over a layer of fibroblast feeder cells or over a layer of anti-MUC1* antibody (C3 or C8 that recognize the N-10 PSMGFR peptide. RT-PCR measurements were performed to quantify the amount of Oct4 expressed under a variety of conditions by Day 4 (
In this series of experiments, we probed the expression of NME6 and NME7 in stem cells and cancer cells. In addition, we identified MUC1* as the target of NME7. We first performed Western blot assays on cell lysates to determine the presence or absence of NME1 and NME7. In
To determine whether NME7 also functions as a growth factor with MUC1* as its target receptor, we performed pull-down assays. In these experiments, a synthetic MUC1* extra cellular domain peptide (His-tagged PSMGFR sequence) was immobilized on NTA-Ni magnetic beads. These beads were incubated with the cell lysates of BGO1v human embryonic stem cells that had been cultured in NME1 dimers over a surface coated with anti-MUC1* antibodies (Lane 1), or cultured in bFGF over MEFs (Lane 2) or T47D human breast cancer cell lysates (Lane 3). Beads were rinsed and captured proteins were released by addition of imidazole. Proteins were separated by SDS-PAGE and then probed with either an anti-NME1 antibody (
NM23 wt was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, XhoI) and cloned between NdeI and XhoI restriction sites of the expression vector pET21b.
NM23-H1 mutant S120G (serine #120 mutated to a glycine) was made using the GeneTailor™ Site-directed mutagenesis system (Life Technologies) following the manufacturer instructions using the following primers: 5′-gcaggaacattatacatggcggtgattctg-3′ (SEQ ID NO:88) and 5′-gccatgtataatgttcctgccaacttgtat-3′ (SEQ ID NO:89).
We generated the NM23-H1 mutant P96S (proline #96 mutated to a serine) using the QuickChange site-directed mutagenesis kit (Agilent) following the manufacturer instructions using the following primers: 5′-tcggggagaccaactctgcagactccaag-3′ (SEQ ID NO:90) and 5′-cttggagtctgcagagttggtctccccga-3′ (SEQ ID NO:91). The template used for the PCR reaction was NM23 wild type cloned between NdeI and XhoI restriction sites. After sequence confirmation, the deletion constructs were generated by PCR. NM23 P96S AC1 was amplified using the following primers: 5′-atcgatcatatggccaactgtgagcgtaccttc-3′ (SEQ ID NO:92) and 5′-gtggtgaccggtatagatccagttctgagcaca-3′ (SEQ ID NO:93). NM23 P96S AC2 was amplified using the following primers: 5′-atcgatcatatggccaactgtgagcgtaccttc-3′ (SEQ ID NO:94) and 5′-gtggtgaccggtgatccagttctgagcacagct-3′ (SEQ ID NO:95). NM23 P96S AC6 was amplified using the following primers: 5′-atcgatcatatggccaactgtgagcgtaccttc-3′ (SEQ ID NO:96) and 5′-gtggtgaccggtagcacagctcgtgtaatctacca-3′ (SEQ ID NO:97). The resulting fragments were purified, digested (NdeI, AgeI) and cloned between NdeI and AgeI restriction sites of the expression vector pET21b. The pET21b was previously modified by replacing the XhoI restriction by AgeI using an overlap PCR method. Optimal dimer formation was observed when NM23-P96S was cloned between NdeI and XhoI. Optimal dimer formation for all deletion mutants was observed when cloned between NdeI and AgeI.
LB broth (Luria-Bertani broth) was inoculated with 1/10 of an overnight culture and cultured at 37° C. until OD600 reached ˜0.5. At this point, recombinant protein expression was induced with 0.4 mM Isopropyl-β-D-thio-galactoside (IPTG, Gold Biotechnology) and culture was stopped after 5 h. After harvesting the cells by centrifugation (6000 rpm for 10 min at 4° C.), cell pellet was resuspended with running buffer: PBS pH7.4, 360 mM NaCl and 80 mM imidazole. Then lysozyme (1 mg/mL, Sigma), MgCl2 (0.5 mM) and DNAse (0.5 ug/mL, Sigma) was added. Cell suspension was incubated on a rotating platform (275 rpm) for 30 min at 37° C. and sonicated on ice for 5 min. Insoluble cell debris was removed by centrifugation (20000 rpm for 30 min at 4° C.). The cleared lysate was then applied to a Ni-NTA column (Qiagen) equilibrated with the running buffer. The column was washed (8 CV) before eluting the protein off the column with the running buffer (6 CV) supplemented with 420 mM imidazole.
For protein denaturation, the elution fractions were pooled and denatured by adding 1 vol of 100 mM Tris pH 8.0+8M urea, the solution was concentrated by half and another vol of 100 mM Tris pH 8.0+8M urea was added. This cycle was repeated until final urea concentration was ˜7M. The protein was then refolded by dialysis.
NM23 supports proliferation of mouse ES cells with pluripotent colony morphology.
Mouse ES cells (129/S6, EMD Millipore, Billerica, Mass.) were cultured on inactivated MEF feeder cell layers for two days in mouse ES cell minimal medium (mESC-MM) supplemented with either 1,000 U/mL recombinant mLIF (a, c) (EMD Millipore) or 16 nM NM23-S120G-RS (b, d), and photographed at low magnification under phase-contrast illumination. Size bars indicate 500 microns. In both cases, single cells and colonies consisting of just a few cells on day 1 give rise to larger multicellular oval colonies with bright, defined edges typical of pluripotent mouse ES cells. mESC-MM consists of KnockOut D-MEM basal medium, 15% KnockOut Serum Replacement, 1× GlutaMax I, 1× OptiMEM non-essential amino acids, 0.1 mM B-ME (Life Technologies, Carlsbad, Calif.), and 1× Penicillin/Streptomycin (Lonza, Allendale, N.J.).
Results are shown in
To determine whether or not human stem cells express NME6 or NME7 in addition to NME1 (H1) and NME2 (H2), we performed Western blot analysis on lysates and supernatant from various human stem cell lines. Human embryonic stem cell line BGO1v cells were cultured either in a) NM23-S120G in dimer form only on a cell culture plate coated with anti-MUC1* monoclonal antibody MN-C3; or b) bFGF at 4 ng/mL on mouse feeder cells (MEFs). After 3 days in culture, the stem cells were harvested and lysed, then analyzed by Western blot using antibodies to probe for the presence of NME1, NME6 and NME7. For comparison, the same analysis was done in parallel on T47D MUC1*-positive breast cancer cells. As a control, recombinant NM23-H1 wild type (NM23-wt) protein was loaded onto the gel and also probed with antibodies that recognize the 3 different NMEs. Note that the gel is a denaturing gel so that the apparent molecular weight of the NM23-S120G dimer and the wild type hexamer will both appear to be the weight of a monomer. The antibodies used to probe the gel were: for NME1: nm23-H1 (C-20); NME6: nm23-H6 (L-17) and NME7: nm23-H7 (B9) (all purchased from Santa Cruz Biotechnology, Inc):
One of the conclusions of this experiment is that NME7 is an earlier form of NM23 that is expressed in a more naïve stem cell. We have already shown that NM23 in dimer form induces stem cells to revert to a more pluripotent state often called the naïve state. Our experiments and those of others have shown that culturing stem cells in bFGF or culturing stem cells over a layer of mouse fibroblast feeder cells (MEFs) drives or maintains stem cells in the less pluripotent state called the “primed” state. Referring to
Western blot analysis of human stem cell lines BGO1v and HES-3 cells shows that an NME antibody, purportedly specific for NME7 recognized NME7 (nm23-H7B9 from Santa Cruz Biotechnology, Inc) and another species that is the same molecular weight as NME6 (anti-NME6 from Abnova) (
Generating recombinant NME7—First constructs were made to make a recombinant NME7 that could be expressed efficiently and in soluble form. The first approach was to make a construct that would encode the native NME7 (−1) or an alternative splice variant NME7 (−2), which has an N-terminal deletion. In some cases, the constructs carried a histidine tag or a strep tag to aid in purification. NME7-1 expressed poorly in E. coli (
Testing recombinant NME7 for ability to maintain pluripotency and inhibit differentiation. A soluble variant of NME7, NME7-AB, was generated and purified as described in Example 9. Human stem cells (iPS cat #SC101a-1, System Biosciences) were grown per the manufacturer's directions in 4 ng/ml bFGF over a layer of mouse fibroblast feeder cells for four passages. These source stem cells were then plated into 6-well cell culture plates (Vita™, Thermo Fisher) that had been coated with 12.5 ug/well of a monoclonal anti-MUC1* antibody, MN-C3. Cells were plated at a density of 300,000 cells per well. The base media was Minimal Stem Cell Media consisting of: 400 ml DME/F12/GlutaMAX I (Invitrogen #10565-018), 100 ml Knockout Serum Replacement (KO-SR, Invitrogen #10828-028), 5 ml 100×MEM Non-essential Amino Acid Solution (Invitrogen #11140-050) and 0.9 ml (0.1 mM) β-mercaptoethanol (55 mM stock, Invitrogen #21985-023). The base media can be any media. In a preferred embodiment, the base media is free of other growth factors and cytokines. To the base media was added either 8 nM of NME7-AB or 8 nM NM23-H1 refolded and purified as stable dimers. Media was changed every 48 hours and due to accelerated growth had to be harvested and passaged at Day 3 post-plating.
The following novel NME6 and NME7 variants were designed and generated:
Human NM23-H7-2 sequence optimized for E. coli expression:
(DNA)
(Amino Acids)
Human NME7-A:
(DNA)
(Amino Acids)
Human NME7-A1:
(DNA)
(Amino Acids)
Human NME7-A2:
(DNA)
(Amino Acids)
Human NME7-A3:
(DNA)
(Amino Acids)
Human NME7-B:
(DNA)
(Amino Acids)
Human NME7-B1:
(DNA)
(Amino Acids)
Human NME7-B2:
(DNA)
(Amino Acids)
Human NME7-B3:
(DNA)
(Amino Acids)
Human NME7-AB:
(DNA)
(Amino Acids)
Human NME7-AB 1:
(DNA)
(Amino Acids)
Human NME7-a Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-A1 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-A2 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-A3 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-B Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-B1 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-B2 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-B3 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-AB Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME7-AB 1 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Mouse NME6
(DNA)
(Amino Acids)
Human NME6:
(DNA)
(Amino Acids)
Human NME6 1:
(DNA)
(Amino Acids)
Human NME6 2:
(DNA)
(Amino Acids)
Human NME6 3:
(DNA)
(Amino Acids)
Human NME6 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME6 1 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME6 2 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
Human NME6 3 Sequence Optimized for E. coli Expression:
(DNA)
(Amino Acids)
NME6 and NME7 as well as novel variants may be expressed with any affinity tag but were expressed with the following tags:
Histidine Tag
Strept II Tag
NME7 wt-cDNA, codon optimized for expression in E. coli was generated per our request by Genscript (NJ). NME7-1 was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, XhoI) and cloned between NdeI and XhoI restriction sites of the expression vector pET21b.
NME7-2 was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, XhoI) and cloned between NdeI and XhoI restriction sites of the expression vector pET21b.
NME7-A was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, XhoI) and cloned between NdeI and XhoI restriction sites of the expression vector pET21b.
NME7-AB was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, XhoI) and cloned between NdeI and XhoI restriction sites of the expression vector pET21b. The protein is expressed with a C-Term His Tag.
NME7-AB was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, AgeI) and cloned between NdeI and AgeI restriction sites of the expression vector pET21b where XhoI was replaced by AgeI followed by the Strep Tag II and two stop codon before the His Tag. The protein is expressed with a C-Term Strep Tag II.
NME6 was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, XhoI) and cloned between NdeI and XhoI restriction sites of the expression vector pET21b. The protein is expressed with a C-Term His Tag.
NME6 was amplified by polymerase chain reaction (PCR) using the following primers:
The fragment was then purified, digested (NdeI, AgeI) and cloned between NdeI and AgeI restriction sites of the expression vector pET21b where XhoI was replaced by AgeI followed by the Strep Tag II and two stop codon before the His Tag. The protein is expressed with a C-Term Strep Tag II.
LB broth (Luria-Bertani broth) is inoculated with 1/10 of an overnight culture and cultured at 37° C. until OD600 reached ˜0.5. At this point, recombinant protein expression is induced with 0.4 mM Isopropyl-β-D-thio-galactoside (IPTG, Gold Biotechnology) and culture is stopped after 5 h. After harvesting the cells by centrifugation (6000 rpm for 10 min at 4° C.), cell pellet is resuspended with running buffer: PBS pH7.4, 360 mM NaCl and 80 mM imidazole. Then lysozyme (1 mg/mL, Sigma), MgCl2 (0.5 mM) and DNAse (0.5 ug/mL, Sigma) is added. Cell suspension is incubated on a rotating platform (275 rpm) for 30 min at 37° C. and sonicated on ice for 5 min. Insoluble cell debris are removed by centrifugation (20000 rpm for 30 min at 4° C.). The cleared lysate is then applied to a Ni-NTA column (Qiagen) equilibrated with the running buffer. The column was washed with 4 CV of running buffer, then 4 CV of running buffer supplemented with 30 mM imidazole before eluting the protein off the column with the running buffer (6 CV) supplemented with 70 mM imidazole followed by a second elution with the running buffer (4 CV) supplemented with 490 mM imidazole. NME7-AB is further purified by size exclusion chromatography (Superdex 200) “FPLC”.
LB broth (Luria-Bertani broth) is inoculated with 1/10 of an overnight culture and cultured at 37° C. until OD600 reached ˜0.5. At this point, recombinant protein expression is induced with 0.4 mM Isopropyl-β-D-thio-galactoside (IPTG, Gold Biotechnology) and culture is stopped after 5 h. After harvesting the cells by centrifugation (6000 rpm for 10 min at 4° C.), cell pellet is resuspended with running buffer: PBS pH7.4, 360 mM NaCl and 80 mM imidazole. Then lysozyme (1 mg/mL, Sigma), MgCl2 (0.5 mM) and DNAse (0.5 ug/mL, Sigma) is added. Cell suspension is incubated on a rotating platform (275 rpm) for 30 min at 37° C. and sonicated on ice for 5 min. Insoluble cell debris are removed by centrifugation (20000 rpm for 30 min at 4° C.). The cleared lysate is then applied to a Ni-NTA column (Qiagen) equilibrated with the running buffer. The column is washed (8 CV) before eluting the protein off the column with the running buffer (6 CV) supplemented with 420 mM imidazole. NME6 is further purified by size exclusion chromatography (Superdex 200) “FPLC”.
Human ES H9 cells (WICELL) were cultured for the indicated number of passages in either 4 ng/mL bFGF (Peprotech) over MEF feeder cells, or in mTeSR (Stem Cell Technologies) over Matrigel, or in 8 nM NM23 (NME1 S120G dimers) in minimal media “MM” wherein cells were plated onto a VITA™ plate (ThermoFisher) that was coated with 12.5 ug/mL C3 anti-MUC1* mab, abbreviated in
A pull down assay using an antibody to the MUC1* cytoplasmic tail (Ab-5) was performed on a panel of cells. The proteins pulled down by the MUC 1 antibody were separated by SDS-PAGE then probed with antibodies specific for NME1, NME6 and NME7, using Western blot technique. MUC1*-positive breast cancer cell line T47D cells (ATCC), human embryonic stem cell line BGO1v (LifeTechnologies), human ES cells (HES-3, BioTime Inc.) and human iPS cells (SC101A-1, System Biosciences Inc.) T47D cancer cells were grown according to ATCC protocol in RPMI-1640 (ATCC) plus 10% FBS (VWR). All stem cells were cultured in minimal stem cell media “MM” with 8 nM NM23-RS (recombinant NME1 S120G dimers). Stem cells were grown on plasticware coated with 12.5 ug/mL anti-MUC1* C3 mab. Cells were lysed with 200 uL RIPA buffer for 10 min on ice. After removal of cell debris by centrifugation, the supernatant was used in a co-immunoprecipitation assay. MUC1* was pulled down using the Ab-5 antibody (anti-MUC-1 Ab-5, Thermo Scientific), which recognizes the MUC1 cytoplasmic tail, coupled to Dynabeads protein G (Life Technologies). The beads were washed twice with RIPA buffer and resuspended in reducing buffer. A sample of the supernatant was subjected to a reducing SDS-PAGE followed by transfer of the protein to a PVDF membrane.
Gold nanoparticles of a diameter of 30.0 nm were coated with an NTA-SAM surface according to Thompson et al. (ACS Appl. Mater. Interfaces, 2011, 3 (8), pp 2979-2987). The NTA-SAM coated gold nanoparticles were then activated with an equal volume of 180 uM NiSO4, incubated for 10 min at room temperature, washed, and resuspended in a 10 mM phosphate buffer (pH 7.4). The gold nanoparticles were then loaded with PSMGFR N-10 peptide (QFNQYKTEAASRYNLTISDVSVSDVPFPFSAQSGAHHHHHH (SEQ ID NO:112)) at 0.5 uM final concentration, and incubated at room temperature for 10 min. Recombinant NME7-AB protein expressed and purified from E. coli was added free in solution at the concentrations indicated. When particle-immobilized proteins bind to each other, or simultaneously bind to two different peptides on two different particles, the particle solution color changes from pink/red to purple/blue. If the protein added free in solution causes particle aggregation, it is strong evidence that the free protein dimerizes the cognate peptide, since binding to a single peptide would not induce two or more particles to be brought into close proximity to each other.
Human ES (HES-3 stem cells, BioTime Inc) and iPS(SC101A-Ipsc, System Biosciences) cells were cultured in Minimal Media (“MM”) plus either NME1 dimers (NM23-RS) or NME7 (NME7-AB construct) for 8-10 passages. The cells were plated onto a Vita™ plate (ThermoFisher) that had been coated with 12.5 ug/mL of an anti-MUC1* monoclonal antibody (MN-C3) that binds to the distal portion of the PSMGFR sequence of the MUC1* receptor. Periodically throughout the 10 passages, samples of the stem cells were assayed by immunocytochemistry (ICC) and analyzed on a confocal microscope (Zeiss LSM 510 confocal microscope) to determine the cellular localization of Histone-3. If Histone-3 is condensed in the nucleus (appears as single dot), then a copy of the X chromosome has been inactivated and the cells are no longer in the pure ground state or naïve state. If the stem cells have reverted from the primed state (all commercially available stem cells have been driven to the primed state by culturing in FGF) to the naïve state, then Histone-3 will be seen as a “cloud,” speckled throughout or not detectable.
A semi-quantitative analysis of the X-activation status of HES-3 stem cells (BioTime Inc) was performed using immunofluorescence images collected on a confocal microscope (Zeiss LSM 510) comparing cells grown on MEFs with 4 ng/ml FGF (p72) versus 8 nM NME1 (p6, p8, p10) versus 8 nM NME7 (p10). 5-6 images of random fields of view at ×20 magnification were collected for each growth factor. Pluripotent stem cells were identified using Oct 3/4 (#sc-5279, Santa Cruz) and/or Nanog (#D73G4, Cell Signaling) staining. Pluripotent stem cells positive for H3K27me3 antibody (marker for Xist; #C36B11, Cell Signaling) were identified by a bright focused spot in the nucleus. Cells negative for H3K27me3 staining either had faint diffuse non-focused staining or it was absent. Total number of cells per image (positive and negative for H3K27me3 staining) were counted using the Cell Counter macro in Image J and data are expressed as a percentage of cells negative for H3K27me3 antibody (i.e. X-activated cells).
Human ES cells (HES-3, BioTime Inc.) and human iPS cells (SC101A-1, System Biosciences Inc.) were cultured in minimal media “MM” plus either NME1-dimers (8 nM) or NME7 (8 nM) for at least 10 passages. Cells were plated onto VITA™ 6-well plates (ThermoFisher) that had been coated with 12.5 μg/mL of a monoclonal anti-MUC1* antibody called “C3” or “MN-C3”. Cells were plated at the following densities: 1,000 cells, 3,000 cells, and 5,000 cells per well. As a control, the same number of cells from the same parent cell line was plated over a layer of MEF feeder cells and cultured in 4 ng/mL bFGF. After 4 to 6 days, the cells were stained with alkaline phosphatase (Leukocyte Alkaline Phosphatase Kit, Sigma-Aldrich) according to package instructions and the number of discrete colonies that arose for each condition was counted. See
Human iPS cells (SC101A-1, System Biosciences Inc.) were plated onto COSTAR plates coated with 12.5 ug/mL of anti-MUC1* mab, C3, and cultured in minimal media (“MM”) or E8 minus FGF and TGF-beta (“MN6”) supplemented with 8 nM NM23-RS (NME1 S120G dimers) or NME7 (NME7-AB), wherein a rho kinase inhibitor (ROCi) was also added to the media (always), only for the first 48 hours, or never (see
Human ES cells (HES-3, BioTime Inc.) plated onto Matrigel were cultured in either MN6 media or MM media supplemented with 8 nM NME7, plus/minus a rho kinase inhibitor (ROCi). For comparison, cells were also cultured in bFGF-containing E8 media. RT-PCR was performed as described above in Example 13 and normalized to the E8 control. Markers of the undesirable primed state are FOXA2, OTX, LHX, and XIST. Markers of the desirable naïve state are OCT4, NANOG, KLF4 and KLF2.
Human ES cells (HES-3, BioTime Inc.) were plated onto a VITA™ plate (ThermoFisher) coated with anti-MUC1* antibody (C3) and cultured in either recombinant human NM23 (NME1 S120G dimers) or NME7-AB in minimal media (MM). RT-PCR performed as described in Example 13. Markers of the undesirable primed state are FOXA2, OTX, LHX, and XIST. Markers of the desirable naïve state are OCT4, NANOG, KLF4 and KLF2. As
Human ES cells (HES-3, BioTime Inc.) were plated onto either a VITA™ plate (ThermoFisher) coated with anti-MUC1* antibody (C3), MEF feeder cells, or Matrigel. Cells on the VITA/C3 antibody surface were cultured for 3 passages in either Minimal Media (MM) plus NM23-H1 S120G dimers (NME1 dimers) or in NME7-AB. Cells plated over MEFs were cultured in MM plus FGF, according to standard practice, for 23 passages. Cells on Matrigel were cultured for a single passage in NME7 in MM media or MN6 media and in the presence or absence of a rho kinase inhibitor (ROCi). Markers of the undesirable primed state are FOXA2, OTX, LHX, and XIST. Markers of the desirable naïve state are OCT4, NANOG, KLF4 and KLF2. As
Human ES cells (BGO1v and HES-3) as well as iPS cells (SC101-A1) were cultured in NME-based media wherein cells were plated over a layer of anti-MUC1* antibody. To identify NME7 species, cells were harvested and lysed with RIPA buffer (Pierce), supplemented with protease inhibitor (Pierce). Cell lysates (20 uL) were separated by electrophoresis on a 12% SDS-PAGE reducing gel and transferred to a PVDF membrane (GE Healthcare). The blot was blocked with PBS-T containing 3% milk and then incubated with primary antibody (anti NM23-H7 clone B-9, Santa Cruz Biotechnology) at 4° C. overnight. After washing with PBS-T, the membrane was incubated with horseradish peroxidase (HRP)-conjugated secondary antibody (goat anti mouse, Pierce) for 1 hr at room temperature. Signals were detected with Immun-Star Chemiluminescence kit (Bio-Rad). The Western blots of
Additionally, human iPS cells (SC101-A1) were cultured as described above or in the presence of siRNA that suppressed OCT4, NME1, NME6 or NME7. The Western blot of
iPS Conditioned media (20 uL) was separated by electrophoresis on either a 12% SDS-PAGE reducing gel and transferred to a PVDF membrane (GE Healthcare). The blot was blocked with PBS-T containing 3% milk and then incubated with primary antibody (anti NM23-H7 clone B-9, Santa Cruz Biotechnology) at 4° C. overnight. After washing with PBS-T, the membrane was incubated with horseradish peroxidase (HRP)-conjugated secondary antibody (goat anti mouse, Pierce) for 1 hr at room temperature. Signals were detected with Immun-Star Chemiluminescence kit (Bio-Rad). Western blot of
A pull down assay was performed using an NME7 specific antibody (NM23 H7 B9, Santa Cruz) on a panel of MUC1*-positive cells. Breast cancer cells (T47D) as well as human ES (BGO1v and HES-3) and iPS(SC101-A1) cells were cultured according to standard protocol (T47D) or cultured in NME-based media over a surface of anti-MUC1* antibody. Cells were lysed with RIPA buffer (Pierce), supplemented with protease inhibitor (Pierce). Cell lysates were supplemented with 10 ug of recombinant NME7-AB incubated at 4° C. for 2 h. Then NME7 was immuno-precipitated at 4° C. overnight with anti NM23-H7 (B-9, Santa Cruz Biotechnology) coupled to Dynabeads protein G (Life technologies). Beads were washed twice with PBS and immuno-precipitated proteins were separated by electrophoresis on a 12% SDS-PAGE reducing gel. Proteins were detected by silver staining (Pierce). The ˜23 kDa bands of proteins that co-immunoprecipitated along with NME7, from the T47D sample and the BGO1v cells, were excised and analyzed by mass spec (Taplin Mass Spectrometry Facility, Harvard Medical School). Mass spec analysis showed that the protein bands that were excised all contained sequences from the NME7 NDPK A domain as shown below. The underlined sequences in the A domain of NME7 were identified by mass spec.
KPDAISKAGEIIEIINK
AGFTITKLKMMMLSRKEALDFHVDHQSRPFFN
GTDGIRNAAHGPDSFASAAR
EMEEFFPSSGGCGPANTAKFTNCTCCIVK
The higher molecular weight protein bands, ˜30 kDa, that immunoprecipitated with NME7 were not analyzed by mass spec and may correspond to either an endogenous NME7 protein that may be a cleavage product or an alternative splice isoform or alternatively could be NME7-AB ˜33 kDa that was added to the cell lysates.
The PSMGFR peptide bearing a C-terminal Cysteine (PSMGFR-Cys) was covalently coupled to BSA using Imject Maleimide activated BSA kit (Thermo Fisher). PSMGFR-Cys coupled BSA was diluted to 10 ug/mL in 0.1M carbonate/bicarbonate buffer pH 9.6 and 50 uL was added to each well of a 96 well plate. After overnight incubation at 4° C., the plate was wash twice with PBS-T and a 3% BSA solution was added to block remaining binding site on the well. After 1 h at RT the plate was washed twice with PBS-T and NME7, diluted in PBS-T+1% BSA, was added at different concentrations. After 1 h at RT the plate was washed 3× with PBS-T and anti-NM23-H7 (B-9, Santa Cruz Biotechnology), diluted in PBS-T+1% BSA, was added at 1/500 dilution. After 1 h at RT the plate was washed 3× with PBS-T and goat anti mouse-HRP, diluted in PBS-T+1% BSA, was added at 1/3333 dilution. After 1 h at RT the plate was washed 3× with PBS-T and binding of NME7 was measured at 415 nm using a ABTS solution (Pierce).
ELISA MUC1* dimerization: The protocol for NME7 binding was used and NME7 was used at 11.6 ug/mL.
After 1 h at RT the plate was washed 3× with PBS-T and HisTagged PSMGFR peptide (PSMGFR-His) or biotinylated PSMGFR peptide (PSMGFR-biotin), diluted in PBS-T+1% BSA, was added at different concentration. After 1 h at RT the plate was washed 3× with PBS-T and anti Histag-HRP (Abcam) or streptavidin-HRP (Pierce), diluted in PBS-T+1% BSA, was added at a concentration of 1/5000. After 1 h at RT the plate was washed 3× with PBS-T and binding of PSMGFR peptide to NME7 already bound to another PSMGFR peptide (which could not signal by anti-His antibody or by streptavidin) coupled BSA was measured at 415 nm using a ABTS solution (Pierce).
WT NME6 cDNA, codon optimized for expression in E. coli was synthesized by our request by Genscript, N.J. The WT NME6 cDNA was then amplified by polymerase chain reaction (PCR) using the following primer: 5′-atcgacatatgacgcaaaatctgggctcggaaatg-3′ (SEQ ID NO:114) and 5′-actgcctcgagtgccggacccagaccacccgtgc-3′ (SEQ ID NO:115). After digestion with NdeI and XhoI restriction enzymes (New England Biolabs), the purified fragment was cloned into the pET21b vector (Novagen) digested with the same restriction enzymes.
LB broth (Luria-Bertani broth) was inoculated with 1/10 of an overnight culture and cultured at 37° C. until OD600 reached ˜0.5. At this point, recombinant protein expression was induced with 0.4 mM Isopropyl-β-D-thio-galactoside (IPTG, Gold Biotechnology) and culture was stopped after 5 h. After harvesting the cells by centrifugation (6000 rpm for 10 min at 4° C.), cell pellet was resuspended with running buffer: PBS pH7.4, 360 mM NaCl, 10 mM imidazole and 8M urea. Cell suspension was incubated on a rotating platform (275 rpm) for 30 min at 37° C. and sonicated on ice for 5 min. Insoluble cell debris was removed by centrifugation (20000 rpm for 30 min at 4° C.). The cleared lysate was then applied to a Ni-NTA column (Qiagen) equilibrated with the running buffer. The column was washed with 4 CV of running buffer, then 4 CV of running buffer supplemented with 30 mM imidazole before eluting the protein off the column with the running buffer (8 CV) supplemented with 420 mM imidazole. The protein was then refolded by dialysis, (
1. Dialyse overnight against 100 mM Tris pH 8.0, 4M urea, 0.2 mM imidazole, 0.4M L-arginine, 1 mM EDTA and 5% glycerol
2. Dialyse 24 h against 100 mM Tris pH 8.0, 2M urea, 0.2 mM imidazole, 0.4M L-arginine, 1 mM EDTA and 5% glycerol
3. Dialyse 24 h against 100 mM Tris pH 8.0, 1M urea, 0.2 mM imidazole, 0.4M L-arginine, 1 mM EDTA and 5% glycerol
4. Dialyse 8 h against 100 mM Tris pH 8.0, 0.2 mM imidazole, 0.4M L-arginine, 1 mM EDTA and 5% glycerol
5. Dialyse overnight against 25 mM Tris pH 8.0, 0.2 mM imidazole, 0.1M L-arginine, 1 mM EDTA and 5% glycerol
6. Dialyse 3×3 h against PBS pH 7.4, 0.2 mM imidazole, 1 mM EDTA and 5% glycerol
7. Dialyse overnight against PBS pH 7.4, 0.2 mM imidazole, 1 mM EDTA and 5% glycerol
8. Centrifuge refolded protein (18,500 rpm) 30 min at 4° C. and collect supernatant for further purification.
The protein was further purified by size exclusion chromatography (Superdex 200).
All of the references cited herein are incorporated by reference in their entirety.
Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention specifically described herein. Such equivalents are intended to be encompassed in the scope of the claims.
| Number | Name | Date | Kind |
|---|---|---|---|
| 8535944 | Bamdad | Sep 2013 | B2 |
| 8859495 | Bamdad | Oct 2014 | B2 |
| 20070243171 | Bunce | Oct 2007 | A1 |
| 20090148535 | Bamdad | Jun 2009 | A1 |
| 20100093092 | Bamdad | Apr 2010 | A1 |
| 20100278788 | Badoer et al. | Nov 2010 | A1 |
| 20100316688 | Bamdad | Dec 2010 | A1 |
| 20110014164 | Huangfu et al. | Jan 2011 | A1 |
| 20120156246 | Bamdad | Jun 2012 | A1 |
| Number | Date | Country |
|---|---|---|
| 2008035110 | Mar 2008 | WO |
| WO 2008070171 | Jun 2008 | WO |
| WO-2009123349 | Oct 2009 | WO |
| WO 2010042891 | Apr 2010 | WO |
| WO-2013059373 | Apr 2013 | WO |
| Entry |
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| Number | Date | Country | |
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| 20150017726 A1 | Jan 2015 | US |
| Number | Date | Country | |
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| 61693712 | Aug 2012 | US | |
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| 61622422 | Apr 2012 | US | |
| 61618578 | Mar 2012 | US | |
| 61548199 | Oct 2011 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2012/060684 | Oct 2012 | US |
| Child | 14254749 | US |
