Patent Grant
11613735
This application a U.S. National stage entry of PCT/CN2015/072232, filed Feb. 4, 2015, which claims benefit of Chinese Provisional Application No. 201410048337.X, filed Feb. 12, 2014, incorporated herein by reference.
The Sequence Listing submitted as a text file named “GHBCL_101_ST25_txt,” created on Feb. 2, 2015, and having a size of 41,627 bytes is hereby incorporated by reference.
The present invention generally relates to use of hepatocyte fate conversion and maturation factors for reprogramming eukaryotic cells into hepatocyte cells.
Functional human cell types are in high demand in the field of regenerative medicine and drug development. They show great potential for repairing or replacing diseased and damaged tissues and can be valuable tools for pharmaceutical applications. However, the application of functional human cell types in these areas is limited due to a shortage of donors (Castell et al., Expert Opin. Drug Metab. Toxicol. 2:183-212 (2006)). To solve this dilemma, novel strategies for generating functionally mature cells are in high demand. Recently, lineage reprogramming has emerged as an effective method for changing the fate of somatic cells (Vierbuchen and Wernig, Mol. Cell, 47: 827-838 (2012)). In principle, one cell type can be converted directly to the final mature state of another cell type and can bypass its intermediate states during lineage reprogramming. Consequently, functionally mature cells may be obtained using this strategy and may potentially provide a promising source of functional human cells.
Functional human hepatocytes are the most significant in vitro model for evaluating drug metabolism and are potentially widely applicable in pharmaceutical development. Because unacceptable metabolic and toxicity effects on the liver are largely responsible for the failure of new chemical entities in drug discovery (Baranczewski et al., Pharmacol. Rep., 58:453-472 (2006)), it is essential to use human hepatocytes, which serve as the closest in vitro model of human liver in assays of absorption, distribution, metabolism, excretion, and toxicity (ADME/Tox), to identify compounds that display favorable pharmacokinetics (Sahi et al., Curr. Drug Discov. Technol., 7:188-198 (2010)). Currently, primary human hepatocytes that are derived from individuals with different genetic backgrounds are frequently used in drug development, but the resulting diversity of genetic backgrounds hinders the reproducibility of the results obtained from pharmaceutical studies using these cells. Additionally, the scarcity of human liver donors greatly limits the use of primary human hepatocytes (Castell et al., Expert Opin. Drug Metab. Toxicol. 2:183-212 (2006)) and, as a result, alternative resources for human hepatocytes with a high reproducibility are urgently required for use in drug discovery.
Different strategies to generate functional hepatocytes have been studied. Human hepatocytes have been derived from human pluripotent stem cells by directed differentiation (Cai et al., Hepatology, 45:1229-1239 (2007); Ogawa et al., Development, 140:3285-3296 (2013); Takebe et al., Nature, 499:481-484 (2013); Zhao et al., Cell Res., 23:157-161 (2013)). This strategy has progressed quickly in recent years, although the immature phenotype of the cells derived from pluripotent stem cells remains a technological obstacle. In principle, fully functional hepatocytes are relatively difficult to obtain using this method, as the whole process involves multiple key steps that affect the final stage of hepatocyte formation. In contrast, lineage reprogramming allows the lineage conversion of a somatic cell without passing through an intermediate state. Although mouse hepatocytes have been transdifferentiated from fibroblasts (Huang et al., Nature, 475:386-389 2011; Sekiya and Suzuki, Nature, 475:390-393 (2011)), these cells still express several hepatoblast markers such as α-fetoprotein (AFP) and lack the expression of several key cytochrome P450 enzymes (CYPs) that are responsible for drug metabolism, suggesting a functionally immature phenotype for these cells (Willenbring, Cell Stem Cell, 9:89-91 (2011)).
There is therefore a need for a method inducing non-hepatocyte cells into functional induced hepatocytes that show improved hepatocyte functional activity, when compared to known induced hepatocytes.
It is therefore an object of the present invention to provide a method of inducing conversion of a non-hepatocyte cell, into an induced hepatocyte cell (iHep) with metabolic function.
It is also an object of the present invention to provide induced hepatic cells with metabolic function.
It is still an object of the present invention to provide a method using induced hepatocytes for drug development, bioartificial liver system and in vivo and in-vitro hepatic applications.
It is further an object of the present invention to provide kits for reprogramming a non-hepatocyte into an iHep.
A method for inducing reprogramming of a cell of a first type which is not a hepatocyte (i.e., non-hepatocyte cells), into a hepatocyte-like cell, as indicated by functional hepatic drug metabolizing and transporting capabilities, is disclosed. These cells are denoted herein as induced hepatocytes (iHeps). The non-hepatocyte is treated to upregulate hepatic fate conversion and maturation factors (“collectively, “Hepatocyte inducing factors”), cultured in somatic cell culture medium (transformation phase), expanded in hepatocyte cell culture medium (expansion phase) and further cultured in hepatocyte maturation medium (maturation phase) for a sufficient period of time to convert the cell into a cell with hepatocyte-like properties.
In a preferred embodiment, the non-hepatocyte cell is transformed to overexpress at least one of the following Hepatocyte inducing factors: Hepatocyte nuclear factor 1-alpha (HNF1A), Hepatocyte nuclear factor 4-alpha (HNF4A), and Hepatocyte nuclear factor 6-alpha (HNF6), Activating transcription factor 5 (ATF5), Prospero homeobox protein 1 (PROX1), and CCAAT/enhancer-binding protein alpha (CEBPA). In some embodiments the cell is transformed to express at least 2, at least 3, at least 4 or at least 5 of the hepatocyte inducing factors. In a preferred embodiment, the cell is transformed to overexpress all 6 Hepatocyte inducing factors. In some embodiments, the method further includes upregulating MYC, and/or downregulating p53 gene expression and/or protein activity. Non-hepatocytes (treated to upregulate hepatocyte inducing factors; and optionally upregulate MYC and optionally, downregulate p53) are then expanded in vitro to obtain iHeps. In one embodiment, transfected cells are cultured in somatic cell culture medium, for example, DMEM, for a period of at least 7 days, until about 80% confluence. The cells are then replated and expanded in hepatocyte cell culture medium (HCM) for about 15 to 30 days, preferably for about 18-30 days, and more preferably, for about 18 days, following which the cells are transferred into a hepatocyte maturation medium for about 5 days. Induced hepatocytes (iHeps) are obtained following this cell culture scheme.
The cells are identified as iheps, based on known structural and functional properties of hepatocytes.
Also disclosed are functional induced hepatocytes (iHeps). In a preferred embodiment, the induced hepatocytes are human induced hepatocytes (hiHeps). iHeps express at least one hepatocyte marker selected from the group consisting of albumin, Cytochrome P450 (Cyp)3A4, CYPB6, CYP1A2, CYP2C9, and CYP2C19. In a preferred embodiment, iHeps express at least two, three or four or five or six of CYPB6, CYP3A4, CYPB6, CYP1A2, CYP2C9, and CYP2C19.
Transplanted hiHeps repopulate up to 30% of the livers of Tet-uPA/Rag2−/−γc−/− mice and secrete more than 300 mg/ml human albumin in vivo. Thus human hepatocytes with drug metabolic function can be generated by lineage reprogramming, thus providing a cell resource for in vitro drug development and in vivo applications within the context of liver disease/failure.
Kits for inducing reprogramming of non-hepatocytes cells into iHeps are also disclosed. The kit includes factors which upregulate the Hepatocyte inducing factors disclosed herein, and optionally, factors which upregulate MYC and downregulate p53 gene expression and/or protein levels.
As used herein a “culture” means a population of cells grown in a medium and optionally passaged. A cell culture may be a primary culture (e.g., a culture that has not been passaged) or may be a secondary or subsequent culture (e.g., a population of cells which have been subcultured or passaged one or more times).
As used herein, “downregulation” or “downregulate” refers to the process by which a cell decreases the quantity and/or activity of a cellular component, for example, DNA, RNA or protein, in response to an external variable.
As used herein, “embryonic stem cell (ESC)-derived hepatocytes (ES-Heps)” refer to induced hepatocytes derived according to the methods disclosed in Zhao, et al., Cell Res., 23(1):157-161 (2013).
As used herein, “functional induced hepatocytes (iHeps)” refers to induced hepatocytes which show the activity of at least one of CYP3A4, CYP2C9, or CYP2C19, at levels 50% higher than the activity of the same enzyme in ES-Heps obtained from the same organism. The activity of the enzyme can be 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100% or more, higher than the activity in ES-Heps.
As used herein, the term “host cell” refers to non-hepatocytes eukaryotic cells into which a recombinant nucleotide, such as a vector, can be introduced.
The term “induced hepatocytes” (iHeps) as used herein refers to cells which are not naturally occurring hepatocytes, and which are artificially derived from non-hepatocyte cells.
The term “isolated” or “purified” when referring to hiHEPS means chemically induced pluripotent stem cells at least 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, or 99% free of contaminating cell types such as non-hepatocyte cells. The isolated iheps may also be substantially free of soluble, naturally occurring molecules.
The terms “oligonucleotide” and “polynucleotide” generally refer to any polyribonucleotide or polydeoxribonucleotide, which may be unmodified RNA or DNA or modified RNA or DNA. Thus, for instance, polynucleotides as used herein refers to, among others, single- and double-stranded DNA, DNA that is a mixture of single- and double-stranded regions, single- and double-stranded RNA, and RNA that is mixture of single- and double-stranded regions, hybrid molecules comprising DNA and RNA that may be single-stranded or, more typically, double-stranded or a mixture of single- and double-stranded regions. The term “nucleic acid” or “nucleic acid sequence” also encompasses a polynucleotide as defined above.
In addition, polynucleotide as used herein refers to triple-stranded regions comprising RNA or DNA or both RNA and DNA. The strands in such regions may be from the same molecule or from different molecules. The regions may include all of one or more of the molecules, but more typically involve only a region of some of the molecules. One of the molecules of a triple-helical region often is an oligonucleotide.
As used herein, the term polynucleotide includes DNAs or RNAs as described above that contain one or more modified bases. Thus, DNAs or RNAs with backbones modified for stability or for other reasons are “polynucleotides” as that term is intended herein. Moreover, DNAs or RNAs comprising unusual bases, such as inosine, or modified bases, such as tritylated bases, to name just two examples, are polynucleotides as the term is used herein.
The term “percent (%) sequence identity” is defined as the percentage of nucleotides or amino acids in a candidate sequence that are identical with the nucleotides or amino acids in a reference nucleic acid sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity. Alignment for purposes of determining percent sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN, ALIGN-2 or Megalign (DNASTAR) software. Appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full-length of the sequences being compared can be determined by known methods.
For purposes herein, the % sequence identity of a given nucleotides or amino acids sequence C to, with, or against a given nucleic acid sequence D (which can alternatively be phrased as a given sequence C that has or comprises a certain % sequence identity to, with, or against a given sequence D) is calculated as follows:
100 times the fraction W/Z,
where W is the number of nucleotides or amino acids scored as identical matches by the sequence alignment program in that program's alignment of C and D, and where Z is the total number of nucleotides or amino acids in D. It will be appreciated that where the length of sequence C is not equal to the length of sequence D, the % sequence identity of C to D will not equal the % sequence identity of D to C
As used herein, “transformed” and “transfected” encompass the introduction of a nucleic acid (e.g. a vector) into a cell by a number of techniques known in the art.
As used herein, a “vector” is a replicon, such as a plasmid, phage, or cosmid, into which another DNA segment may be inserted so as to bring about the replication of the inserted segment. The vectors described herein can be expression vectors.
As used herein, an “expression vector” is a vector that includes one or more expression control sequences.
“Reprogramming” as used herein refers to the conversion of a one specific cell type to another. For example, a cell that is not a hepatocyte cab be reprogrammed into a cell that is morphologically and functionally like a hepatocyte.
As used herein “treating a cell/cells” refers to contacting the cell(s) with factors such as the nucleic acids disclosed herein to downregulate or upregulate the quantity and/or activity of a cellular component, for example, DNA, RNA or protein. This phrase also encompasses contacting the cell(s) with any factors including proteins and small molecules that can downregulate or upregulate the gene/protein of interest.
The term “upregulate expression of” means to affect expression of, for example to induce expression or activity, or induce increased/greater expression or activity relative to an untreated cell.
As used herein, “upregulation” or “upregulate” refers to the process by which a cell increases the quantity and/or activity of a cellular component, for example, DNA, RNA or protein, in response to an external variable.
“Variant” refers to a polypeptide or polynucleotide that differs from a reference polypeptide or polynucleotide, but retains essential properties. A typical variant of a polypeptide differs in amino acid sequence from another, reference polypeptide. Generally, differences are limited so that the sequences of the reference polypeptide and the variant are closely similar overall and, in many regions, identical. A variant and reference polypeptide may differ in amino acid sequence by one or more modifications (e.g., substitutions, additions, and/or deletions). A substituted or inserted amino acid residue may or may not be one encoded by the genetic code. A variant of a polypeptide may be naturally occurring such as an allelic variant, or it may be a variant that is not known to occur naturally.
A. Factors Inducing Non-Hepatocyte Cells into Hepatocyte-Like Properties
Obtaining fully functional cell types is a major challenge for drug discovery, bioartificial liver and regenerative medicine. Currently, a fundamental solution to this key problem is still lacking. Functional human induced hepatocytes (hiHeps) can be generated from fibroblasts by upregulating at least one factor selected from the group consisting of HNF1A, HNF4A, HNF6, ATF5, PROX1, and CEBPA, as well as MYC genes mRNA or protein levels. All known functional variants and isoforms of the hepatocyte inducing factors disclosed herein are contemplated. These known sequences are readily available in the National Center for Biotechnology Information Genebak database.
Preferably, p53 activity is additionally, downregulated as indicated by a downregulation of the p53 gene, mRNA and/or protein levels.
1. Nucleic Acids Encoding Hepatocyte Inducing Factors
i. HNF1A
HNF1A (also known as TCF1) is a tumor suppressor gene involved in liver tumorigenesis. It is located on the long arm of chromosome 12, encoded by 10 exons, spanning 23 kilobases, and is expressed in various tissues, including liver, kidney, pancreas, and digestive tract. It encodes a transcription factor HNF1, which, in the liver, is implicated in hepatocyte differentiation and is required for expression of certain liver-specific genes, including albumin, β-fibrinogen, and α1-antitrypsin. Courtois, et al., Science, 30(4827:688-692 (1987). The HNF1A gene is conserved in chimpanzee, Rhesus monkey, dog, cow, mouse, rat, chicken, zebrafish, and frog.
In a preferred embodiment, a nucleotide encoding HNF1A is represented below by SEQ ID NO:1.
A nucleic acid encoding HNF1A can include a sequence having at least 80%, 85%, 90%, 95%, 99%, or 100% sequence identity to SEQ ID NO:1 or a functional fragment or variant of SEQ ID NO:1.
A number of naturally occurring variants of nucleic acids encoding HNF1A and their activities are known in the art, and include, but are not limited to, the transcript variant for HNF1A as represented by GenBank Accession No: XM_005253931.1.
ii. HNF6
HNF6 was originally characterized as a transcriptional activator of the liver promoter of the 6-phosphofructo-2-kinase (pfk-2) gene, is expressed in liver, brain, spleen, pancreas, and testis. Lannoy, et al., J. Biol. Chem., 273:13552-13562 (1998). Alternative splicing results in multiple transcript variants.
In one embodiment, HNF6 is represented by SEQ ID NO:2.
A nucleic acid encoding HNF6 can include a sequence having at least 80%, 85%, 90%, 95%, 99%, or 100% sequence identity to SEQ ID NO:2 or a functional fragment or variant of SEQ ID NO:2.
A number of naturally occurring variants of nucleic acids encoding HNF6 and their activities are known in the art. A human hepatocyte nuclear factor 6 (HNF6) gene is described under NCBI GenBank Accession No. AF035581. A Homo sapiens transcript variant mRNA is disclosed under Genbank Accession No. NM_004498.2.
iii. HNF4A
Hepatocyte nuclear factor 4 alpha (HNF4alpha, NR2A1, gene symbol HNF4A) is a highly conserved member of the nuclear receptor (NR) superfamily of ligand-dependent transcription factors (Sladeck, et al., Genes Dev., 4(12B): 2353-65 (1990). HNF4A1 is expressed in liver (hepatocytes), kidney, small intestine, etc. HNF4A2 is the most predominant isoform in the liver. HNF4A regulates most if not all of the apolipoprotein genes in the liver and regulates the expression of many cytochrome P450 genes (e.g., CYP3A4, CYP2D6) and Phase II enzymes and hence may play a role in drug metabolism (Gonzalez, et al., Drug Metab. Pharmacokinet., 23(1):2-7 (2008).
In one embodiment, HNF4 is represented by SEQ ID NO:3.
A nucleic acid encoding HNF4 can include a sequence having at least 80%, 85%, 90%, 95%, 99%, or 100% sequence identity to SEQ ID NO:3 or a functional fragment or variant of SEQ ID NO:3.
A number of naturally occurring variants of nucleic acids encoding HNF4 and their activities are known in the art. A human hepatocyte nuclear factor 4 gene is described under NCBI GenBank Accession No. BC137539.1.
iv. ATF5
ATF5 encodes activating transcription factor 5. ATF5 transcripts and protein are expressed in a wide variety of tissues, in particular, high expression of transcripts in liver.
In one embodiment, ATF5 is represented by SEQ ID NO:4.
A nucleic acid encoding ATF5 can include a sequence having at least 80%, 85%, 90%, 95%, 99%, or 100% sequence identity to SEQ ID NO:4 or a functional fragment or variant of SEQ ID NO:4. A number of naturally occurring variants of nucleic acids encoding ATF5 and their activities are known in the art. A human ATF5 transcript variant 3 (mRNA) is described under Genbank Accession No. NM_001290746.1 (Abe, et al., J. Biol. Chem., 289(7):3888-3900 (2014)).
v. PROX1
In one embodiment, PROX1 is represented by SEQ ID NO:5.
A nucleic acid encoding PROX1 can include a sequence having at least 80%, 85%, 90%, 95%, 99%, or 100% sequence identity to SEQ ID NO:5 or a functional fragment or variant of SEQ ID NO:5. A number of naturally occurring variants of nucleic acids encoding PROX1 and their activities are known in the art.
vi. CEBPA
CEBPA encodes a basic leucine zipper (bZIP) transcription factor which can bind as a homodimer to certain promoters and enhancers.
In one embodiment, CEBPA is represented by SEQ ID NO:6.
A nucleic acid encoding CEBPA can include a sequence having at least 80%, 85%, 90%, 95%, 99%, or 100% sequence identity to SEQ ID NO:6 or a functional fragment or variant of SEQ ID NO:6. A number of naturally occurring variants of nucleic acids encoding CEBPA and their activities are known in the art.
vii. MYC
Myc (c-Myc) is a regulator gene that codes for a transcription factor, which is multifunctional, nuclear phosphoprotein that plays a role in cell cycle progression, apoptosis and cellular transformation.
In one embodiment, MYC is represented by SEQ ID NO:7.
2. Vectors Encoding Hepatocyte Inducing Factors
The Hepatocyte inducing factors are introduced into a host cell using suitable transformation vectors. Nucleic acids, such as those described above, can be inserted into vectors for expression in cells. As used herein, a “vector” is a replicon, such as a plasmid, phage, virus or cosmid, into which another DNA segment may be inserted so as to bring about the replication of the inserted segment. Vectors can be expression vectors. An “expression vector” is a vector that includes one or more expression control sequences, and an “expression control sequence” is a DNA sequence that controls and regulates the transcription and/or translation of another DNA sequence.
Nucleic acids in vectors can be operably linked to one or more expression control sequences. For example, the control sequence can be incorporated into a genetic construct so that expression control sequences effectively control expression of a coding sequence of interest. Examples of expression control sequences include promoters, enhancers, and transcription terminating regions. A promoter is an expression control sequence composed of a region of a DNA molecule, typically within 100 nucleotides upstream of the point at which transcription starts (generally near the initiation site for RNA polymerase II). To bring a coding sequence under the control of a promoter, it is necessary to position the translation initiation site of the translational reading frame of the polypeptide between one and about fifty nucleotides downstream of the promoter. Enhancers provide expression specificity in terms of time, location, and level. Unlike promoters, enhancers can function when located at various distances from the transcription site. An enhancer also can be located downstream from the transcription initiation site. A coding sequence is “operably linked” and “under the control” of expression control sequences in a cell when RNA polymerase is able to transcribe the coding sequence into mRNA, which then can be translated into the protein encoded by the coding sequence.
Suitable expression vectors include, without limitation, plasmids and viral vectors derived from, for example, bacteriophage, baculoviruses, tobacco mosaic virus, herpes viruses, cytomegalo virus, retroviruses, vaccinia viruses, adenoviruses, lentiviruses and adeno-associated viruses. Numerous vectors and expression systems are commercially available from such corporations as Novagen (Madison, Wis.), Clontech (Palo Alto, Calif.), Stratagene (La Jolla, Calif.), and Invitrogen Life Technologies (Carlsbad, Calif.).
B. Cells to be Induced
Cells that can be reprogrammed include embryonic stem cells (ESC), induced pluripotent stem cells (iPSC), fibroblast cells, adipose-derived stem cells (ADSC), neural derived stem cells, blood keratinocytes, intestinal epithelial cells and other non-hepatocyte somatic cells. In a preferred embodiment, the non-hepatocyte cell is a fibroblast cell, for example an embryonic fibroblasts (HEFs) or foreskin fibroblasts. The cells are preferably obtained from a mammal, for example, rat, mice, monkeys, dogs, cats, cows, rabbits, horses, pigs Preferably, the cells are obtained from a human subject.
C. Induced Hepatocyte Cells
iHeps are disclosed, which are obtained for example, by a method which includes treating non-hepatocyte cells to overexpress the hepatic fate conversion factors HNF1A, HNF4A, and HNF6 along with the maturation factors ATF5, PROX1, and CEBPA. The non-hepatocyte is treated to overexpress at least one hepatocyte inducing factor selected from the group consisting of HNF1A, HNF4A, HNF6, ATF5, PROX1, and CEBPA. In some embodiments the non-hepatocyte is treated to overexpress or transformed to express at least 2, at least 3, at least 4 or at least 5 of the hepatocyte inducing factors. In a preferred embodiment, the cell is transformed to overexpress all 6 Hepatocyte inducing factors.
iHeps show typical and functional characteristics of hepatocytes in the organisms from which the cell induced was obtained. For example, iHeps show the typical morphology for primary human hepatocytes. iHeps express at least one hepatic marker selected from the group consisting of albumin, Cytochrome P450 (Cyp)3A4 and CypB6. Like primary human hepatocytes, hiHeps express an additional spectrum of phase I and II drug-metabolizing enzymes and phase III drug transporters and albumin. The metabolic activities of at least one of CYP3A4, CYPB6, CYP1A2, CYP2C9, and CYP2C19 are comparable between hiHeps and freshly isolated primary human hepatocytes. Preferably, the iHeps are functional as determined by the metabolic activity of these enzymes being at least 50% higher than the activity of the same enzyme in ES-Heps obtained from the same organism. The activity of the enzyme can be 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95%, 100% or more, higher than the activity in ES-Heps. Most preferably, the activities of all these CYP enzymes in hiHeps are at least 100-fold higher than that of ES-Heps.
In some embodiments, MYC expression levels in iHeps are lower than the levels found in normal hepatocytes in the corresponding organism as measured for example, by quantitative reverse transcriptase polymerase chain reaction (RT-qPCR), i.e., if the donor organism for the non-hepatocyte cell to be induced is a human subject, the levels are compared to normal hepatocytes found in humans.
Functional hiHeps may also express at least one drug metabolic phase II enzyme or phase II transporter selected from the group consisting of UDP glucuronosyltransferase (UGT)1A1, UGT1A3, UGT1A4, UGT1A6, UGT1A9, GSTA1, UGT2B7, UGT2515, Microsomal glutathione-S-transferase 1 (MGST1), nicotinamide N-methyltransferase (NNMT), NTCP, organic anion-transporting polypeptide 1B3 (OATP1B3), Multidrug resistance protein(MRP)6, MRP2, Flavin-containing monooxygenase 5 (FMO5), Monoamine oxidase (MAO)A, MAOB, and epoxide hydrolase 1 (EPHX1). Preferably, endogenous expression of Forkhead box (FOX)A1, FOXA2, FOXA3 and Liver receptor homolog 1 (LRH1) is activated in hiHeps.
In some embodiment where the cell being induced is not an epithelial cell, hiHeps additionally express at least one epithelial cell marker, for example, E-cadherin, and where the cell being induced is a fibroblast, the hiHeps obtained following induction of fibroblasts using the methods disclosed herein, do not express the fibroblast marker genes such as COLIA1, PDGFRB, THY1 and α-fetoprotein as measured for example by RT-PCR.
With respect to functional characteristics associated with mature hepatocytes, hiHeps possess at least one characteristic selected from the group consisting of: albumin secretion, LDL uptake, indocyanine green (ICG) incorporation from cell culture medium and exclusion of the absorbed ICG after withdrawal, glycogen synthesis and storage, and fatty droplet accumulation.
Huang, et al., Nature, 475:386-389 (2011) disclose the direct induction of hepatocyte-like cells from mouse tail-tip fibroblasts by transduction of Gata4, Hnf1α and Foxa3, and inactivation of p19(Arf). Induced cells show typical epithelial morphology. Sekiya and Suzuki, Nature, 475:390-393 (2011)), identified three specific combinations of two transcription factors, Hnf4α plus Foxa1, Foxa2 or Foxa3, that can convert mouse embryonic and adult fibroblasts into cells that resemble hepatocytes in vitro. Cai, et al., Hepatology, 45(5):1229-39 (2007) disclose a three-stage method to direct the differentiation of human embryonic stem cells (hESCs) into hepatic cells in serum-free medium. Human ESCs were first differentiated into definitive endoderm cells by 3 days of Activin A treatment. Next, the presence of fibroblast growth factor-4 and bone morphogenetic protein-2 in the culture medium for 5 days induced efficient hepatic differentiation from definitive endoderm cells, followed by 10 days of further in vitro maturation. Zhao, et al., Cell Res., 23(1):157-161 (2013) disclose a method of promoting the maturation of hESCs into cells with hepatocyte-like properties by inducing expression of PROX1 and HNF6.
In the methods disclosed herein, the non-hepatocyte is reprogrammed into an iHep by upregulating Hepatocyte inducing factors in the cell, optionally in combination with upregulating MYC and downregulating p53 and culturing the cells for a sufficient period of time as disclosed herein to convert the cell into a cell with hepatocyte-like properties. The non-hepatocyte cells to be induced are obtained from the donor animal using methods known in the art. The cells are placed in culture and cultured using methods that are known in the art.
The reprogramming method includes the following steps: (a) treat the cells to upregulate hepatocyte inducing factors and culture the cells in cell culture medium (transformation phase); (b) replate and culture the cells in HCM (expansion phase), and (c) a maturation phase, where cells are cultured in a hepatocyte maturation medium. A schematic for the disclosed method is shown in
In the transformation phase, the treated cells are cultured for a sufficient length of time in conventional cell culture medium, for example, Dulbecco's Modified Eagle's medium (DMEM). Preferably, the cells are cultured for at least 7 days in this first step, to about 80% confluence. The cells then replated and expanded in HCM for a period of about 15 to 30 days, preferably for about 18-30 days, and more preferably, for about 18 days (expansion phase), and then transferred to modified William's E medium for a period of about 5 days (maturation phase), following which induced hepatocytes are harvested. Preferably, p53 siRNA is downregulated at the end of the expansion phase, for example at about day 20-30 post infection, preferably, at about day 25 post infection, before the cells are transferred into the modified William's E medium (
The method includes a step confirming that the non-hepatocytes have acquired hepatocyte-like properties, using morphological and functional characteristics as well as gene expression.
Morphological confirmation methods include the confirmation of morphological characteristics specific for hepatocytes such as cells having a plurality of nuclei observed by a phase microscope and granules rich in cytoplasm observed by an electron microscope, in particular, the presence of glycogen granules.
Treated cells can also be identified as induced hepatocytes using one or more of the following characteristics: their ability to express ALB at a level comparable to that of primary human hepatocytes; expression of one or more of the five major cytochrome P450 enzymes, CYP3A4, CYP1A2, CYP2C9, and CYP2C19; expression of phase II enzyme or phase II transporter selected from the group consisting of UGT1A1, UGT1A3, UGT1A4, UGT1A6, UGT1A9, GSTA1, UGT2B7, UGT2515, MGST1, NNMT, NTCP, OATP1B3, MRP6, MRP2, FMO5, MAOA, MAOB, and EPHX1. Successful induction can be confirmed by the presence of an epithelial marker and the absence of a marker for the cell which is being induced. For example, where the cell being induced is a fibroblast, additional indication that the cells has been induced into a hepatocyte-like cell can be expression of at least one epithelial cell marker, for example, E-cadherin, and absence of expression of the fibroblast marker genes such as COLIA1, PDGFRB, THY1 and α-fetoprotein as measured for example by RT-PCR.
A. Upregulating Hepatocyte Inducing Factors and MYC
Hepatocyte inducing factors and MYC are upregulated by contacting the non-hepatocyte with factors which upregulate gene expression and or protein levels/activity of the Hepatocyte inducing Factors and MYC. These factors include, but are not limited to nucleic acids, proteins and small molecules.
For example, upregulation may be accomplished by exogenously introducing the nucleic acids encoding the hepatocyte inducing Factor(s) and optionally, MYC, into the non-hepatocyte (host cell). The nucleic acid may be homologous or heterologous. The nucleic acid molecule can be DNA or RNA, preferably, mRNA. Preferably, the nucleic acid molecule is introduced into the non-hepatocyte cell by lentiviral expression.
The host cell is transformed to overexpress at least one hepatocyte inducing factor selected from the group consisting of HNF1A, HNF4A, HNF6, ATF5, PROX1, and CEBPA. Preferably, the cell is additionally transformed overexpress the proliferation factor MYC. In some embodiments the cell is transformed to express at least 2, at least 3, at least 4 or at least 5 of the hepatocyte inducing factors. In a preferred embodiment, the cell is transformed to overexpress all 6 Hepatocyte inducing factors.
Vectors containing nucleic acids to be expressed can be transferred into host cells. Nucleic acids can be transfected into mammalian cells by techniques including, for example, calcium phosphate co-precipitation, DEAE-dextran-mediated transfection, lipofection, electroporation, or microinjection. The Ex vivo methods disclosed herein can include, for example, the steps of harvesting cells from a subject/donor, culturing the cells, transducing them with an expression vector, and maintaining the cells under conditions suitable for expression of the encoded polypeptides. These methods are known in the art of molecular biology.
Upregulation may also be accomplished by treating the cells with factors known to increase expression of genes encoding the Hepatocyte inducing factors/MYC and/or factors known to increase the corresponding protein levels. For example, Zhao, et al., Cell Res., 23(1):157-161 (2013), disclose a method for promoting the emergence of PROX1 and HNF6-expressing cells from hESCs using the induction factors FGF7, BMP2 and BMP4. Known factors, including small molecules and/or proteins which upregulate Hepatocyte inducing factors gene expression or protein levels can also be use.
B. Downregulating p53
p53 can be downregulated by treating cells to downregulate p53 gene expression, mRNA levels or protein levels. This step includes contacting the cells with any molecule that is known to downregulate p53 gene expression, mRNA or protein levels, including but not limited to nucleic acid molecules, small molecules and protein.
p53 gene expression can be inhibited using a functional nucleic acid, or vector encoding the same, selected from the group consisting of antisense oligonucleotides, siRNA, shRNA, miRNA, EGSs, ribozymes, and aptamers. Preferably, p53 gene expression is inhibited using siRNA, shRNA, or miRNA.
1. RNA Interference
In some embodiments, P53 gene expression is inhibited through RNA interference. Gene expression can also be effectively silenced in a highly specific manner through RNA interference (RNAi). This silencing was originally observed with the addition of double stranded RNA (dsRNA) (Fire, et al. (1998) Nature, 391:806-11; Napoli, et al. (1990) Plant Cell 2:279-89; Hannon, (2002) Nature, 418:244-51). Once dsRNA enters a cell, it is cleaved by an RNase III-like enzyme, Dicer, into double stranded small interfering RNAs (siRNA) 21-23 nucleotides in length that contains 2 nucleotide overhangs on the 3′ ends (Elbashir, et al. (2001) Genes Dev., 15:188-200; Bernstein, et al. (2001) Nature, 409:363-6; Hammond, et al. (2000) Nature, 404:293-6). In an ATP dependent step, the siRNAs become integrated into a multi-subunit protein complex, commonly known as the RNAi induced silencing complex (RISC), which guides the siRNAs to the target RNA sequence (Nykanen, et al. (2001) Cell, 107:309-21). At some point the siRNA duplex unwinds, and it appears that the antisense strand remains bound to RISC and directs degradation of the complementary mRNA sequence by a combination of endo and exonucleases (Martinez, et al. (2002) Cell, 110:563-74). However, the effect of iRNA or siRNA or their use is not limited to any type of mechanism.
Short Interfering RNA (siRNA) is a double-stranded RNA that can induce sequence-specific post-transcriptional gene silencing, thereby decreasing or even inhibiting gene expression. In one example, a siRNA triggers the specific degradation of homologous RNA molecules, such as mRNAs, within the region of sequence identity between both the siRNA and the target RNA. For example, WO 02/44321 discloses siRNAs capable of sequence-specific degradation of target mRNAs when base-paired with 3′ overhanging ends, herein incorporated by reference for the method of making these siRNAs.
Sequence specific gene silencing can be achieved in mammalian cells using synthetic, short double-stranded RNAs that mimic the siRNAs produced by the enzyme dicer (Elbashir, et al. (2001) Nature, 411:494 498) (Ui-Tei, et al. (2000) FEBS Lett 479:79-82). siRNA can be chemically or in vitro-synthesized or can be the result of short double-stranded hairpin-like RNAs (shRNAs) that are processed into siRNAs inside the cell. Synthetic siRNAs are generally designed using algorithms and a conventional DNA/RNA synthesizer. Suppliers include Ambion (Austin, Tex.), ChemGenes (Ashland, Mass.), Dharmacon (Lafayette, Colo.), Glen Research (Sterling, Va.), MWB Biotech (Esbersberg, Germany), Proligo (Boulder, Colo.), and Qiagen (Vento, The Netherlands). siRNA can also be synthesized in vitro using kits such as Ambion's SILENCER® siRNA Construction Kit.
The production of siRNA from a vector is more commonly done through the transcription of a short hairpin RNAse (shRNAs). Kits for the production of vectors comprising shRNA are available, such as, for example, Imgenex's GENESUPPRESSOR™ Construction Kits and Invitrogen's BLOCK-IT™ inducible RNAi plasmid and lentivirus vectors.
2. Antisense
p53 gene expression can be inhibited by antisense molecules. Antisense molecules are designed to interact with a target nucleic acid molecule through either canonical or non-canonical base pairing. The interaction of the antisense molecule and the target molecule is designed to promote the destruction of the target molecule through, for example, RNAse H mediated RNA-DNA hybrid degradation. Alternatively the antisense molecule is designed to interrupt a processing function that normally would take place on the target molecule, such as transcription or replication. Antisense molecules can be designed based on the sequence of the target molecule. There are numerous methods for optimization of antisense efficiency by finding the most accessible regions of the target molecule. Exemplary methods include in vitro selection experiments and DNA modification studies using DMS and DEPC. It is preferred that antisense molecules bind the target molecule with a dissociation constant (Kd) less than or equal to 10−6, 10−8, 10−10, or 10−12.
An “antisense” nucleic acid sequence (antisense oligonucleotide) can include a nucleotide sequence that is complementary to a “sense” nucleic acid encoding a protein, e.g., complementary to the coding strand of a double-stranded cDNA molecule or complementary to the p53 encoding mRNA. Antisense nucleic acid sequences and delivery methods are well known in the art (Goodchild, Curr. Opin. Mol. Ther., 6(2):120-128 (2004); Clawson, et al., Gene Ther., 11(17):1331-1341 (2004)). The antisense nucleic acid can be complementary to an entire coding strand of a target sequence, or to only a portion thereof. An antisense oligonucleotide can be, for example, about 7, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, or more nucleotides in length.
An antisense nucleic acid sequence can be designed such that it is complementary to the entire p53 mRNA sequence, but can also be an oligonucleotide that is antisense to only a portion of the p53 mRNA. An antisense nucleic acid can be constructed using chemical synthesis and enzymatic ligation reactions using procedures known in the art. For example, an antisense nucleic acid (e.g., an antisense oligonucleotide) can be chemically synthesized using naturally occurring nucleotides or variously modified nucleotides designed to increase the biological stability of the molecules or to increase the physical stability of the duplex formed between the antisense and sense nucleic acids, e.g., phosphorothioate derivatives and acridine substituted nucleotides can be used. The antisense nucleic acid also can be produced biologically using an expression vector into which a nucleic acid has been subcloned in an antisense orientation (i.e., RNA transcribed from the inserted nucleic acid will be of an antisense orientation to a target nucleic acid of interest, described further in the following subsection).
Other examples of useful antisense oligonucleotides include an alpha-anomeric nucleic acid. An alpha-anomeric nucleic acid molecule forms specific double-stranded hybrids with complementary RNA in which, contrary to the usual beta-units, the strands run parallel to each other (Gaultier et al., Nucleic Acids. Res. 15:6625-6641 (1987)). The antisense nucleic acid molecule can also comprise a 2′-o-methylribonucleotide (Inoue et al. Nucleic Acids Res. 15:6131-6148 (1987)) or a chimeric RNA-DNA analogue (Inoue et al. FEBS Lett., 215:327-330 (1987)).
3. Aptamers
In some embodiments, the inhibitory molecule is an Aptamer. Aptamers are molecules that interact with a target molecule, preferably in a specific way. Aptamers can bind the target molecule with a very high degree of specificity. For example, aptamers have been isolated that have greater than a 10,000 fold difference in binding affinities between the target molecule and another molecule that differ at only a single position on the molecule. Because of their tight binding properties, and because the surface features of aptamer targets frequently correspond to functionally relevant parts of the protein target, aptamers can be potent biological antagonists. Typically aptamers are small nucleic acids ranging from 15-50 bases in length that fold into defined secondary and tertiary structures, such as stem-loops or G-quartets. Aptamers can bind small molecules, such as ATP and theophiline, as well as large molecules, such as reverse transcriptase and thrombin. Aptamers can bind very tightly with Kd's from the target molecule of less than 10−12 M. It is preferred that the aptamers bind the target molecule with a Kd less than 10−6, 10−8, 10−10, or 10−12. It is preferred that the aptamer have a Kd with the target molecule at least 10, 100, 1000, 10,000, or 100,000 fold lower than the Kd with a background binding molecule. It is preferred when doing the comparison for a molecule such as a polypeptide, that the background molecule be a different polypeptide.
4. Ribozymes
p53 gene expression can be inhibited using ribozymes. Ribozymes are nucleic acid molecules that are capable of catalyzing a chemical reaction, either intramolecularly or intermolecularly. It is preferred that the ribozymes catalyze intermolecular reactions. There are a number of different types of ribozymes that catalyze nuclease or nucleic acid polymerase type reactions which are based on ribozymes found in natural systems, such as hammerhead ribozymes. There are also a number of ribozymes that are not found in natural systems, but which have been engineered to catalyze specific reactions de novo. Preferred ribozymes cleave RNA or DNA substrates, and more preferably cleave RNA substrates. Ribozymes typically cleave nucleic acid substrates through recognition and binding of the target substrate with subsequent cleavage. This recognition is often based mostly on canonical or non-canonical base pair interactions. This property makes ribozymes particularly good candidates for target specific cleavage of nucleic acids because recognition of the target substrate is based on the target substrates sequence.
5. Triplex Forming Oligonucleotides
p53 gene expression can be inhibited using triplex forming molecules. Triplex forming functional nucleic acid molecules are molecules that can interact with either double-stranded or single-stranded nucleic acid. When triplex molecules interact with a target region, a structure called a triplex is formed in which there are three strands of DNA forming a complex dependent on both Watson-Crick and Hoogsteen base-pairing. Triplex molecules are preferred because they can bind target regions with high affinity and specificity. It is preferred that the triplex forming molecules bind the target molecule with a Kd less than 10−6, 10−8, 10−10, or 10−12.
6. External Guide Sequences
p53 expression can be inhibited using external guide sequences. External guide sequences (EGSs) are molecules that bind a target nucleic acid molecule forming a complex, which is recognized by RNase P, which then cleaves the target molecule. EGSs can be designed to specifically target a RNA molecule of choice. RNAse P aids in processing transfer RNA (tRNA) within a cell. Bacterial RNAse P can be recruited to cleave virtually any RNA sequence by using an EGS that causes the target RNA:EGS complex to mimic the natural tRNA substrate. Similarly, eukaryotic EGS/RNAse P-directed cleavage of RNA can be utilized to cleave desired targets within eukaryotic cells. Representative examples of how to make and use EGS molecules to facilitate cleavage of a variety of different target molecules are known in the art.
7. ShRNA
p53 expression can be inhibited using small hairpin RNAs (shRNAs), and expression constructs engineered to express shRNAs. Transcription of shRNAs is initiated at a polymerase III (pol III) promoter, and is thought to be terminated at position 2 of a 4-5-thymine transcription termination site. Upon expression, shRNAs are thought to fold into a stem-loop structure with 3′ UU-overhangs; subsequently, the ends of these shRNAs are processed, converting the shRNAs into siRNA-like molecules of about 21 nucleotides (Brummelkamp et al., Science 296:550-553 (2002); Lee et al., Nature Biotechnol. 20:500-505 (2002); Miyagishi and Taira, Nature Biotechnol. 20:497-500 (2002); Paddison et al., Genes Dev. 16:948-958 (2002); Paul et al., Nature Biotechnol. 20:505-508 (2002); Sui (2002) supra; Yu et al., Proc. Natl. Acad. Sci. USA 99(9):6047-6052 (2002).
C. Delivery Vehicles
Methods of making and using vectors for in vivo expression of functional nucleic acids such as antisense oligonucleotides, siRNA, shRNA, miRNA, EGSs, ribozymes, and aptamers are known in the art.
For example, the delivery vehicle can be a viral vector, for example a commercially available preparation, such as an adenovirus vector (Quantum Biotechnologies, Inc. (Laval, Quebec, Canada). The viral vector delivery can be via a viral system, such as a retroviral vector system which can package a recombinant retroviral genome. The recombinant retrovirus can then be used to infect and thereby deliver to the infected cells nucleic acid encoding the hepatocyte inducing factor(s). The exact method of introducing the altered nucleic acid into the host cell is, of course, not limited to the use of retroviral vectors. Other techniques are widely available for this procedure including the use of adenoviral vectors, adeno-associated viral (AAV) vectors, lentiviral vectors, pseudotyped retroviral vectors, and others described in (Soofiyani, et al., Advanced Pharmaceutical Bulletin, 3(2):249-255 (2013). Viruses can be modified to enhance safety, increase specific uptake, and improve efficiency (see, for example, Zhang, et al., Chinese J Cancer Res., 30(3):182-8 (2011), Miller, et al., FASEB J, 9(2):190-9 (1995), Verma, et al., Annu Rev Biochem., 74:711-38 (2005)).
Physical transduction techniques can also be used, such as liposome delivery and receptor-mediated and other endocytosis mechanisms (see, for example, Schwartzenberger et al., Blood, 87:472-478 (1996)). Commercially available liposome preparations such as LIPOFECTIN, LIPOFECTAMINE (GIBCO-BRL, Inc., Gaithersburg, Md.), SUPERFECT (Qiagen, Inc. Hilden, Germany) and TRANSFECTAM (Promega Biotec, Inc., Madison, Wis.), as well as other liposomes developed according to procedures standard in the art are well known. In addition, nucleic acid or vectors encoding the hepatocyte inducing factors can be delivered in vivo by electroporation as well as by means of a sonoporation. During electroporation electric pulses are applied across the cell membrane to create a transmembrane potential difference, allowing transient membrane permeation and transfection of nucleic acids through the destabilized membrane (Soofiyani, et al., Advanced Pharmaceutical Bulletin, 3(2):249-255 (2013)). Sonoporation combines the local application of ultrasound waves and the intravascular or intratissue administration of gas microbubbles to transiently increase the permeability of vessels and tissues (Escoffre, et al., Curr Gene Ther., 13(1):2-14 (2013)). Electroporation and ultrasound based techniques are targeted transfection methods because the electric pulse or ultrasound waves can be focused on a target tissue or organ and hence gene delivery and expression should be limited to thereto. Expression or overexpression of the disclosed hepatocyte inducing factors accomplished with any of these or other commonly used gene transfer methods, including, but not limited to hydrodynamic injection, use of a gene gun.
The studies disclosed herein show that human hepatocytes with drug metabolic function can be generated by lineage reprogramming, thus providing a cell resource for pharmaceutical applications.
A. In Vitro and Research Applications
(1) Drug Testing
Liver parenchymal cells play a key role in drug development because the liver plays a central role in the metabolic activity of the drug. At present, the main cause of failure of a drug candidate is its ADME (absorption, distribution, metabolism, excretion) is not ideal. An essential part of drug discovery research is to the metabolic and toxicological effects of the candidate drug on liver cells, human liver parenchymal cells with full participation of drug metabolism. Currently the main hepatocytes used for in vitro drug development are human adult primary hepatocytes. Due to their limited sources, and the difficulty of maintaining primary hepatocyte function in vitro is difficult to maintain, their application in drug development is quite limited, hiHeps disclosed herein which express phase I, II and III drug-metabolizing enzymes can be used in vitro drug metabolism studies.
(ii) Research
The problem encountered in studies involving infectious diseases is the lack of adequate animal models. hiHeps can be used to construct humanized mouse models for study of infectious diseases, for example, hepatitis B and C infections. These animal models can provide a reliable in vivo platform for use in the development of vaccines and drugs for treating infectious diseases, particularly diseases that infect the liver.
B. In Vivo Applications
Liver failure and loss of function is one of the most severe consequences of liver disease. Because of its rapid onset, rapid progression, liver transplantation is the primary means of treatment of these diseases. However, donor scarcity presents a serious problem and many patients die while waiting for liver transplantation.
The studies disclosed herein show that transplanted hiHeps repopulate up to 30% of the livers of Tet-uPA/Rag2−/−γc−/− mice and secrete more than 300 mg/ml human albumin in vivo. Thus, hiHeps can be used in the treatment of liver failure and loss of function diseases, for example.
Transplanting isolated iHeps by percutaneous or transjugular infusion into the portal vein, or injecting into the splenic pulp or the peritoneal cavity, is a less invasive procedure compared with liver transplantation. The iHeps are preferably obtained from the same animal being treated. As the host liver is not removed or resected, the loss of graft function should not worsen liver function. Furthermore, isolated iHeps could be, potentially, cryopreserved for ready access. The iHeps can be used as a vehicle for ex vivo gene therapy for example, for rescuing patients from radiation-induced liver damage resulting from radiotherapy for liver tumors. iHeps can be transplanted into a recipient organism using a carrier such as a matrix known for transplantation of hepatocytes. For example, Zhou, et al., Liver Transpl., 17(4):418-27 (2011) discloses the use of decellularized liver matrix (DLM) as a carrier for hepatocyte transplantation. Schwartz, et al., Int. J. Gastroentrol., 10(1): discloses isolating liver and pancreas cells from tissue samples, seeding onto a poly-L-lactic acid matrix and re-implanting into the mesentery of the same patient.
hiHeps can also be used in the bio-artificial liver support systems. Bioartificial liver support system based on the disclosed cells are constructed to temporarily replace the main function of liver failure (remove hazardous substances, provide the liver synthetic biologically active substances), to stabilize and improve the patient's internal environment, until a suitable donor source for transplantation is available. Methods for making bioartifical liver are disclosed for example in U.S. Publication No. 2008/0206733.
Kits for inducing in vitro reprogramming of non-hepatocytes into induced heptocytes with functional hepatocyte metabolic properties are disclosed. The kit includes factors which up-regulate hepatocyte inducing factors HNF1A, HNF6, HNF4A, ATF5, PROX1, CEPBA, and/or MYC and factors which downregulate p53 gene expression and/or protein activity. In one embodiment, the kit includes any DNA sequence of HNF1A, HNF6, HNF4A, ATF5, PROX1, CEPBA, and/or MYC and DNA sequence to downregulate p53 gene expression. In a preferred embodiment, the kit includes lentiviruses which overexpress HNF1A, HNF6, HNF4A, ATF5, PROX1, CEPBA, and/or MYC gene and nucleic acid which inhibits p53 gene expression.
Materials and Methods
Human Primary Cell Isolation and Culture
The present study was approved by the Clinical Research Ethics Committee of China-Japan Friendship Hospital (Ethical approval No: 2009-50), Stem Cell Research Oversight of Peking University (SCRO201103-03) and conducted according to the principles of the Declaration of Helsinki.
Human embryonic skins and fetal liver tissues at 14 gestational weeks were obtained from abortion with informed patient consent. Fetal liver cells were obtained as previously described (Lilja et al., 64:1240-1248 (1997)). The fetal liver tissue was cut into 1-3 mm3 fragments for digestion in 10 ml medium (RPMI 1640) supplemented with 1 mg/ml collagenase IV (Gibco). Digestion was performed at 37° C. for 15-20 min and erythrocytes were eliminated by slow-speed centrifugation. Cells were washed with RPMI 1640 medium for 3 times. Trypan blue exclusion estimated that cell viability was 90%.
Fresh human embryonic skin tissue (HEF) and ex vivo human adult foreskin tissue (HFF) were sterilized with 75% aqueous ethanol and washed with phosphate buffered saline (PBS). The tissue was carefully separated from subcutaneous tissue with ophthalmic scissors. The tissue was washed several times with PBS, small tissue blocks were seeded in a petri dish, and placed in an incubator at 37° C., 5% CO2. Two hours later, the following were added: DMEM high glucose medium (purchased from Hyclone company, product catalog No. SH30022.01B), 15% fetal bovine serum (FBS), 0.1 mM β-mercaptoethanol, 1% non-essential amino acids, and 1 mM Glutamate, 8 units/ml gentamicin). Cells were digested with 0.25% trypsin and 0.02% EDTA at room temperature for 5 minutes. Cells were seeded at 1:3 in the above-described DMEM high glucose medium in a new Petri dish. Medium was changed every two days, and cells were passaged 1:3 every 4 days to obtain human fibroblasts (derived from fetal skin) and human fibroblasts (derived from adult foreskin). Human skin fibroblasts get to about 80% confluence following cell culture for about 5-7 days.
Human primary hepatocytes were isolated from human donor livers not used for liver transplantation, following informed consent (Seglen, 13:29-83 (1976)) and cultured with HCM (LONZA).
Generation of hiHeps
This study was approved by the Clinical Research Ethics Committee of the China-Japan Friendship Hospital (ethical approval 2009-50) and Stem Cell Research Oversight of Peking University (SCRO201103-03), and conducted according to the principles of the Declaration of Helsinki.
Human fibroblasts were infected overnight and cultured in DMEM plus 10% fetal bovine serum for 1 week before transfer into hepatocyte culture medium (HCM) (Lonza) for expansion.
One day before viral infection, human fibroblasts were seeded at 20,000 cells/well into 12-well cell culture plates containing mammalian somatic cell culture medium, and cultured at 37° C. and 5% carbon dioxide culture for 12 hours; then thereto was added the following lentivirus expression vectors: lentivirus expression vectors expressing HNF1A, HNF6, HNF4A, ATF5, PROX1, CEBPA and MYC, respectively and a lentivirus expressing a DNA(s) for inhibiting the expression of p53, 10 μl for HNF1A, 10 μl for HNF6, 6 μl for HNF4A, 10 μl for ATF5, 3 μl for PROX1, 3 μl for CEBPA, 10 μl for MYC and 10 μl for p53 (lentivirus for inhibiting the expression of p53). The medium was changed after 20 hours, after which the medium was changed every day. Cells were cultured for 7 days in DMEM and then transferred into HCM.
After 3 weeks of culture, HCM was replaced by modified William's E medium (Beijing Vitalstar Biotechnology). Cells were passaged every 4 days, and human hepatocyte-like cells were harvested after 30 days. A schematic for hiHep reprogramming is shown in
Growth Curve and Doubling Times
For MTT assays, the induced cells of expansion stage and maturation stage were plated into 96-well plate (1000 cells per well) and cultured in HCM (before p53 siRNA-GFP silence) or modified WEM (after p53 siRNA-GFP silence) separately for 7 days. MTT assay was done at each day according to the manufacturer's instructions (Vybrant® MTT Cell Proliferation Assay Kit, Invitrogen). To calculate the doubling time of the induced cells in the expansion stage, the induced cells in the expansion stage (before p53 siRNA-GFP silence) were plated at the density of 30000 cells per well, and cultured in 12-well plate coated with matrigel. The growth rate was determined by counting the number of cells using a hemacytometer as a function of time. Data from the exponential phase of growth (data points at 12, 24, 36 and 48 h) were used to obtain an exponential growth curve. Doubling time (Td) was then obtained using the formula: Td=t*ln 2/ln(Nt/N0) where Nt is the cell number at time t; NO is the cell number at the initial time.
Hepatic Differentiation
Human embryonic stem cells (hESCs, ES cell line H1, WiCell research institute) were maintained on irradiated mouse embryonic fibroblasts in hESCs medium (Thomson et al., Science 282:1145-1147 (1998)). hESCs were differentiated into hepatocytes as previously reported (Zhao et al., Cell Res 23:157-161 (2013)).
Molecular Cloning, Lentivirus Production and Transduction
Complementary DNAs of transcriptional factors are amplified from the human full-length TrueClones™ (Origene) and inserted into pCDH-EF1-MCS-T2A-Puro (System Biosciences) according to user's manual (for each of lentivirus expression vectors of HNF1A, HNF6, HNF4A, ATF5, PROX1, and CEBPA, SEQ ID NOs: 1-6 are inserted into restriction enzyme sites of pCDH-EF1-MCS-T2A-Puro, respectively). Lentivirus expression vector of MYC is constructed by inserting SEQ ID NO:7 into restriction enzyme sites (Xho I and EcoR I) of expression vector pLL-IRES-Puro (Zhao Y et al., Cell Stem Cell. 2008 Nov. 6; 3(5): 475-9; available from Beijing Vitalstar Biotechnology, Ltd. or Peking University. For full sequence information, see http://www.sciencegateway.org/protocols/lentivirus/pllmap.html). Lentivirus for inhibiting the expression of p53 is constructed as follows: DNA molecule for interfering with the expression of p53 is inserted into restriction enzyme sites (Hpa I and Xho I) of expression vector pll3.7 (Rubinson and Dillon et al., Nature Genetics, 2003; available from Beijing Vitalstar Biotechnology, Ltd. or Peking University). The DNA molecule for interfering with the expression of p53 is obtained by annealing with a sense chain (5′-TGACTCCAGTGGTAATCTACTTCAAGAGAGTAGATTACCACTGGA GTCTTTTTTC-3′) and a antisense chain (5′-TC GAGAAAAAAGACTCCAGTGGTAATCTACTCTCTTG AAGTAGATTACCACTGGAGT CA-3′). Virus package is conducted as described previously (Zhao et al., Cell Stem Cell, 3:475-479 (2008)). Human fibroblasts are infected in DMEM (Hyclone) with 10% fetal bovine serum, containing 10 μg/ml polybrene for 12 hours. The fibroblasts were replated seven days post infection and cultured in HCM (LONZA). At about 25 days post infection when p53 siRNA was silenced as indicated by a GFP reporter, hiHeps were cultured in modified William's E Medium (Vitalstar Biotechnology).
Albumin ELISA, Periodic Acid-Schiff (PAS) Staining, Indocyanine Green (ICG) Uptake and Release, Low-Density Lipoprotein (LDL) Uptake and Oil Red Staining
Human Albumin was measured using the Human Albumin ELISA Quantitation kit (Bethyl Laboratory). The PAS staining system was purchased from Sigma-Aldrich. Cultures were fixed with 4% paraformaldehyde (DingGuo) and stained according to the manufacturer's instructions. ICG uptake and release was performed as previously described (Cai et al., Hepatology 45:1229-1239 (2007)). For LDL uptake assay, 10 μg/ml DiI-Ac-LDL (Invitrogen) was incubated with hiHeps for 4 h at 37° C. and observed by fluorescence microscopy. For lipid detection, cultures were fixed with 4% paraformaldehyde and treated with 60% isopropanol for 5 min. Then the isopropanol was removed and Oil Red O working solution was added and incubated for 15 min at room temperature. Then the Oil Red O was removed and cultures rinsed with until clear.
CYP Metabolism Assay
Drug metabolic activity was evaluated using the traditional suspension method as previously described (Gebhardt et al., Drug Metab. Rev. 35:145-213 (2003)). hiHeps were cultured in the medium with 50 mM rifampicin, 50 mMb-naphthoflavone, and 1 m Mphenobarbital for 72 hr and refreshed every 24 hr. Cell viability of dissociated hiHeps, HepG2 cells, ES-Heps, fibroblasts, and freshly isolated primary human hepatocytes was measured by trypan blue. One milliliter of prewarmed incubation medium (William's E medium, 10 mM HEPES [pH 7.4], 2 mM GlutaMAX) was added per 1 3 106 total cells (cell suspension). The substrate solutions were prepared with the same incubation medium [400 mM testosterone, 10 mM midazolam, 200 mM phenacetin, 1 mM bupropion, 500 mM (S)-mephenytoin, 50 mM diclofenac]. The reactions were started by mixing 250 ml of the substrate solution with 250 ml of cell suspension in a 5 ml polystyrene round-bottom tube (BD Falcon). The tubes were put in an orbital shaker in the incubator and the shaker speed was adjusted to 210 rpm. After a 15-240 min incubation at 37° C., the tubes were centrifuged at room temperature to collect the supernatant. The reactions were stopped by addition of sample aliquots to tubes containing triple the volume of quenching solvent (methanol) and frozen at −80° C. Isotope-labeled reference metabolites were used as internal standards. Internal reference metabolites for testosterone, midazolam, (S)-mephenytoin, diclofenac, bupropion, and phenacetin are 6b-hydroxytestosterone-[D7], hydroxymidazolam-[13C3], 40-hydroxymephenytoin-[D3], 40-hydroxydiclofenac-[13C6], hydroxybupropion-[D6], and acetomidophenol-[13C2, 15N], respectively. The metabolites were used to make standard curves for the metabolite analyses. Standard metabolites were 6b-hydroxytestosterone, 10-hydroxymidazolam, hydroxybupropion, 40-hydroxydiclofenac, (±)-40-hydroxymephenytoin, and acetaminophen. The metabolites were quantified by Pharmaron using validated traditional LC-MS methods. The results are expressed as picomoles of metabolite formed per minute and per million cells. Chemicals were purchased from Sigma including b-naphthoflavone, rifampicin, testosterone, midazolam, diclofenac, and phenacetin. Standard metabolites and internal reference metabolites were purchased from BD Biosciences. Phenobarbital was a kind gift from Jinning Lou.
qRT-PCR and RT-PCR
Total RNA was isolated by RNeasy Micro Kit (Qiagen) and then reverse-transcribed with SuperScript® III First-Strand Synthesis (Invitrogen). RT-PCR was performed with 2×EasyTaq PCR SuperMix (TransGen) following the manufacturer's instructions. Primers used for specific detection of endogenous gene expression are shown in Tables 1 and 2.
qRT-PCR was performed using Power SYBR® Green PCR Master Mix (Applied Biosystems) on MX3000P Sequence Detection System (Stratagene). Primers used are shown in Table 3.
Primer for 18s rRNA was purchased from QIAGEN. Quantified values were normalized against the input determined by two housekeeping genes (GAPDH or RRN18S). For the positive control in qRT-PCR, five different batches of fresh isolated primary human hepatocytes were collected in RNAprotect (Qiagen) and stored at −20° C. Total RNA was isolated and then reverse-transcribed to cDNA as described above. Equal volumes of cDNA obtained from five different batches of freshly isolated primary human hepatocytes were mixed to be taken as the positive control.
Immunofluorescence and Flow Cytometric Analysis
Cells or tissue sections were fixed in 4% paraformaldehyde (Dingguo) at room temperature for 15 minutes and blocked with PBS containing 0.25% Triton X-100 and 5% normal donkey serum (Jackson ImmunoResearch Laboratories, Inc) at room temperature for 1 hour or at 4° C. overnight. Samples were incubated with primary antibodies at 4° C. overnight, washed three times with PBS and then incubated with appropriate secondary antibodies for 1 hour at room temperature in the dark. Nuclei were stained with DAPI (Roche). Experiments were repeated for three times and typical results were shown. The primary antibodies used for immuno-fluorescence are as follows: rabbit anti CYP3A4, rabbit anti CYP2C9, rabbit anti YP1A2, rabbit anti CYP2E1, rabbit anti CYP2D6 (all from AbD Serotec), Goat anti ALB (Bethyl Laboratories, INC), Rabbit anti NR5A2/LRH1 (Abeam), Rabbit anti COL1A1 (Abeam), Mouse anti E-CAD (Abeam), Mouse anti human nuclei (Millipore). The secondary antibodies used for immunofluorescence are as follows: DyLight® 550 Donkey anti rabbit and DyLight® 550 Donkey anti goat (from Abeam), DyLight 488 donkey anti goat Dylight 549 donkey anti goat, DyLight 488 donkey anti mouse, Dylight 549 donkey anti mouse, DyLight 488 donkey anti rabbit, Dylight 549 donkey anti rabbit (all from Jackson ImmunoResearch Laboratories). Flow cytometric assays were conducted as reported previously (Zhao et al., Cell Res., 23:157-161 (2013)).
RNA-Sequence Analysis
Total RNA was isolated from HEFs, HepG2 cells, ES-Heps, hiHeps and freshly isolated primary human hepatocytes. RNA sequencing libraries were prepared with the Illumina TruSeq RNA Sample Preparation Kit. The fragmented and randomly primed 200-bp paired-end libraries were sequenced on Illumina HiSeq 2000 sequencing system.
Toxicity Assays.
hiHeps were incubated with various concentrations of compounds dissolved in culture medium for 24 h. Cell viability was measured by MTT assay (Invitrogen) following the manufacturer's instructions and as described previously (Khetani and Bhatia, Nat Biotechnol 26, 120-126 (2008)).
Animals and Transplantation
Tet-uPA/Rag2−/−/γc−/− mice on a BALB/c background were purchased from Beijing Vitalstar Biotechnology. hiHeps, ES-Heps, and primary human hepatocytes (2×106 cells/animal) were injected into the spleens of the mice. Blood samples were collected and human ALBUMIN was quantified using the Human Albumin ELISA Quantitation kit (Bethyl Laboratories). Livers of recipient mice were embedded in OCT compound (Sakura) and then frozen in liquid nitrogen. Cryostat sections (10 mm) were stained.
Statistical Analysis
For statistical analysis, a two-tailed unpaired t test was used. Results are expressed as mean±SD. p values are as follows: *p<0.05; **p<0.01; ***p<0.001.
Accession Numbers
RNA-sequencing data have been deposited in the NCBI Gene Expression Omnibus database under accession number GSE54066.
Results
Identification of Factors that Induce Hepatic Fate
To identify the combination of transcription factors that induce human embryonic fibroblasts (HEFs) into hepatocytes, a pool of transcription factors (Table 4) that were previously shown to be expressed in human hepatocytes and are crucial to the determination of hepatic cell fate was selected (Nagaoka and Duncan, Prog. Mol. Biol Transl Sci., 97:79-101 (2010); Zaret, Nat. Rev. Genet., 9:329-340 (2008)).
Previous studies also showed that proliferation arrest and cell death are general barriers to cell reprogramming (Huang et al., Nature, 475:386-389 (2011); Zhao et al., Cell Stem Cell, 3:475-479 (2008)). Thus, MYC was employed in the reprogramming process, as well as p53 small interfering RNA (siRNA) was employed in the reprogramming process. Briefly, HNF1A and HNF4A are preferentially considered because of their critical role in both embryonic and adult liver among the 17 transcription factors. Then additional factors were screened using a “2+1” strategy by the addition of one candidate factor at a time to the combination of HNF1A and HNF4A.
The data showed that HNF6, cooperating with HNF4A and HNF1A, can result in a high percentage of Albumin (ALB)-positive cells within 20 days (data not shown). These three factor induced hepatocyte-like cells (3H cells) exhibited some hepatic properties, including glycogen synthesis and low-density lipoprotein (LDL) uptake (data not shown). However, the expression level of ALB in these cells was extremely low (
Identification of Factors that Generate Mature Hepatocytes
To identify the factors capable of inducing the functional maturation of hepatocyte-like cells, a global gene expression analysis was performed on 3H cells, freshly isolated primary human hepatocytes (F-HEPs), and fetal liver cells. Differential expression of several hepatic transcription factors, including CEBPA, ATF5, and PROX1, was observed among the three samples (data not shown). These three genes were expressed at relatively low levels in the 3H cells and in fetal hepatocytes compared to the levels in adult hepatocytes. This difference was further confirmed by quantitative PCR (
To generate mature human hepatocytes from fibroblasts, the three factors with CEBPA, PROX1, and ATF5, were combined, and overexpressed in HEFs following the scheme shown in
hiHeps Possess the Typical Characteristics of Human Hepatocytes
To evaluate hepatic fate conversion, typical hepatic features were first analyzed. Immunofluorescence microscopy showed that the epithelial marker E-cadherin (ECAD) was coexpressed with ALB in hiHeps (data not shown). In addition, the fibroblast marker COL1A1 was not detected (data not shown). These results indicate a successful mesenchymal-epithelial transition in hiHeps. Next, endogenous hepatic transcription network activation in hiHeps was further examined using RT-PCT.
The RT-PCR results showed that the endogenous expression of FOXA1, FOXA2, and FOXA3 (Zaret et al., Nat. Rev. Genet., 9:329-340 (2008)) was activated in iHeps (
The expression of FOXA2 and LRH1 was confirmed using immunofluorescence (data not shown). Additionally, fibroblast marker genes, including COL1A1, PDGFRB, and THY1, were not detected in hiHeps (
Next, hiHeps was evaluated for functional characteristics of human hepatocytes. hiHeps were competent for LDL uptake (data not shown). In addition, hiHeps could incorporate indocyanine green (ICG) from the medium and exclude the absorbed ICG after withdrawal (data not shown). Oil red O staining in hiHeps showed an accumulation of fatty droplets, and Periodic Acid-Schiff (PAS) staining indicated glycogen synthesis (data not shown). Similar to human adult hepatocytes, hiHeps were AFP negative (data not shown). G banding analysis revealed that hiHeps had a normal karyotype after 7 weeks of culture (data not shown). Besides HEFs, similar results were obtained when adult foreskin fibroblasts were converted as described herein using the same factors (data not shown). Collectively, these results indicate that hiHeps exhibit typical hepatic functional features.
The global gene expression patterns in hiHeps and F-HEPs were compared by RNA sequencing. Principle component analysis and hierarchical clustering analysis revealed that hiHeps established from different donors were clustered with human hepatocytes and separated from human fibroblasts, HepG2 cells, and human embryonic stem cell (ESC)-derived hepatocytes (ES-Heps) (data not shown). Indeed, hepatic transcription factors were upregulated (As it is depicted in
Establishment of the Central Network of Drug Metabolism in hiHeps
To evaluate whether hiHeps expressed key enzymes in drug metabolism, the expression in hiHeps of five key CYP enzymes, CYP1A2, CYP2B6, CYP2C9, CYP2C19, and CYP3A4 in hiHeps was quantitatively confirmed. The five key CYPs are major phase I enzymes that account for 60% of human drug oxidation (Zhou et al., Drug Metab. Rev., 41:89-295 (2009)). As the positive control, pooled F-HEPs from five individual donors were used. Notably, comparable mRNA levels of these major CYPs could be detected in hiHeps and F-HEPs, in contrast to their expression in hepatocytes derived from human ESCs and HepG2 cells (
Level of Key Drug Metabolic Activities in hiHeps is Comparable to that in Freshly Isolated Primary Human Hepatocytes
To evaluate the drug metabolic activities of hiHeps, the studies first focused on CYP3A4. Using ultraperformance liquid chromatography-tandem mass spectrometry technology, the drug metabolic activity of CYP3A4 in hiHeps was detected by using two structurally different substrates, testosterone and midazolam. Because of the remarkable interindividual variability in drug clearance, two batches of freshly isolated primary human hepatocytes were used as the positive control. In contrast to the HepG2 cell line, ES-Heps, and HEFs, hiHeps were able to metabolize the two CYP3A4-selective substrates efficiently and the metabolism efficiency is comparable to the metabolism seen with freshly isolated hepatocytes (F-HEPs) (
To further evaluate the functional central network of drug metabolism in hiHeps, the expression of nuclear receptors between hiHeps and F-HEPs, which are critical in regulating the expression of metabolizing enzymes, was compared. Nuclear receptors that are responsible for the xenobiotic metabolizing system were expressed in hiHeps (
To assess the potential application of hiHeps in studying hepatotoxicity, acute toxicity of model hepatotoxins were quantified. As hepatotoxicity is the most common adverse event resulting in drug failure (Sahi et al., Curr. Drug Discov. Technol., 7:188-198 2010), the sensitivity of drug toxicity is a key index for the potential application of human hepatocytes in drug discovery. hiHeps showed a level of sensitivity comparable to that of primary human hepatocytes when incubated with a series of model hepatotoxins (
Repopulation of Tet-uPA/Rag2−/−γc−/− Mouse Liver with hiHeps
To investigate the capacity of hiHeps to repopulate mouse liver, Tet-uPA (urokinase-type plasminogen activator)/Rag2−/−/γc−/− mice were injected intrasplenically with hiHeps (Song et al., Am. J. Pathol., 175:1975-1983 (2009)). The secretion of human Albumin in mouse serum increased gradually and the highest level reached was 313 mg/ml at 7 weeks after hiHep transplantation (
Discussion
These studies show that human hiHeps are readily and reproducibly generated from HEFs using a combination of hepatic fate conversion factors HNF1A, HNF4A, and HNF6 together with the maturation factors ATF5, PROX1, and CEBPA. Similar to primary human hepatocytes, hiHeps exhibit many typical hepatic features, including their epithelial morphology, expression of hepatocyte specific markers, basic functional properties of hepatocytes, and global gene expression patterns. Importantly, an integral spectrum of phase I and phase II drug-metabolizing enzymes and phase III drug transporters is well established in hiHeps. Furthermore, transplanted hiHeps can repopulate up to 30% of the livers of Tet-uPA/Rag2−/−/γc−/− mice and secrete more than 300 mg/ml human albumin in vivo. This data shows that human hepatocytes with drug-metabolizing functions can be generated from fibroblasts using lineage reprogramming. One key question in lineage reprogramming is how to obtain fully functional cells. In hepatic transdifferentiation, mouse induced hepatocyte-like cells were generated with several important hepatic characteristics, through the expression of hepatic fate determination factors in fibroblasts (Huang et al., 2011; Sekiya and Suzuki, Nature, 475:390-393 (2011)). However, incomplete hepatocyte differentiation and expression of certain hepatoblast markers by hiHeps are compatible with an immature or progenitor-like state (Willenbring, Cell Stem Cell, 9:89-91 (2011)). These studies also show that that certain hepatic fate determination factors could reprogram HEFs into hepatocyte-like cells. However, these cells are not functional until the addition of three additional factors (
The drug metabolic capacity of human hepatocytes is one of the most important functions that distinguish hepatocytes from other lineages and has broad applications in drug development. Efforts to differentiate human pluripotent stem cells into hepatocytes have resulted in cells that were functionally immature. A recent study showed that human ES-Heps express CYP1A2 and CYP3A4 (Zhao et al., Cell Res., 23:157-161 (2013)). However, the activities of these two CYP enzymes were significantly lower than that of primary hepatocytes. In another study, differentiated hepatocytes exhibited CYP3A4 and CYP1A2 activities only comparable to that of cultured primary hepatocytes (Ogawa et al., Development, 140:3285-3296 2013). However, a number of liver-essential functions were progressively lost with time in cultured primary hepatocytes (Elaut et al., Curr. Drug Metab. 7:629-660 (2006)). In the studies disclosed herein, the gold standard, freshly isolated primary human hepatocytes, was used as the positive control. The hiHeps disclosed herein express the key phase I (CYP3A4, CYP2C9, CYP2C19, CYP2B6, and CYP1A2) and phase II drug-metabolizing enzymes and phase III drug transporters at a level comparable to that of freshly isolated primary human hepatocytes. Importantly, the metabolic activities of the five CYP enzymes in hiHeps were comparable to those in freshly isolated primary human hepatocytes, indicating the potential application of hiHeps in evaluating drugs metabolized by these CYP enzymes (
Another key characteristic of human hepatocytes in drug development is their sensitivity to drug toxicity. Human hepatocytes derived from human pluripotent stem cells have a relatively low sensitivity to drug toxicity (Zhao et al., Cell Res., 23:157-161 (2013)). By contrast, the sensitivity of hiHeps disclosed herein to multiple model hepatotoxins is comparable to that of primary human hepatocytes (
Hepatocyte transplantation is a promising alternative to orthotopic liver transplantation (Dhawan et al., Nat Rev Gastroenterol Hepatol, 7:288-298 (2010)). However, the limited supply of donor organs that can provide good-quality cells remains a major challenge. In the studies described herein, hiHeps were able to repopulate mouse liver robustly and secreted up to 313 mg/ml human ALBUMIN, which is two orders of magnitude higher than recent studies using human hepatocytes derived from human embryonic stem cells (
In conclusion, human hepatocytes were generated with drug metabolizing functions using the combined expression of cell fate determination factors and cell maturation factors. The generation of functional human hepatocytes with lineage reprogramming provides a way to obtain well-characterized, reproducible, and functional human hepatocytes for pharmaceutical applications.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201410048337.X | Feb 2014 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2015/072232 | 2/4/2015 | WO |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2015/120776 | 8/20/2015 | WO | A |
| Number | Name | Date | Kind |
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| 20110195056 | Pryor | Aug 2011 | A1 |
| 20110280844 | Yu | Nov 2011 | A1 |
| 20120196360 | Okita | Aug 2012 | A1 |
| 20120231490 | Mizuguchi | Sep 2012 | A1 |
| 20130071365 | Suzuki | Mar 2013 | A1 |
| 20140242595 | Yu | Aug 2014 | A1 |
| Number | Date | Country |
|---|---|---|
| 2013252081 | Jun 2013 | JP |
| 0244321 | Jan 2002 | WO |
| 2011016588 | Feb 2011 | WO |
| 2011130402 | Oct 2011 | WO |
| 2012058868 | May 2012 | WO |
| 2014039768 | Mar 2014 | WO |
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