Patent Application
20230158079
The present invention relates to a composition for treating ischemic diseases or neuroinflammatory diseases containing neural progenitor cells or secretome thereof as active ingredient.
Stem cells are regarded as a promising therapeutic candidate material for various diseases due to the multipotency thereof. For example, mesenchymal stem cells (MSCs) release many nutritional factors that can be easily obtained and isolated and achieve the promotion of angiogenesis and the inhibition of inflammation (Caplan, A. I., & Dennis, J. E. (2006). Journal of Cellular Biochemistry, 98, 1076-1084). These characteristics of MSCs have been considered in studies for the application to the treatment of a number of human diseases. Recent studies have found that MSCs contribute to the tissue repair in a large number of animal models and human clinical treatments (Chen, J., Li, Y., Katakowski, M., et al. (2003). Journal of Neuroscience Research, 73, 778-786; Kopen, G. C., Prockop, D. J., & Phinney, D. G. (1999). Proceedings of the National Academy of Sciences, 96, 10711-10716). Several reports stated the in vitro differentiation ability of MSC into the neural lineage (Bae, K. S., Park, J. B., Kim, H. S., Kim, D. S., Park, D. J., & Kang, S. J. (2011). Yonsei Medical Journal, 52, 401-412) and astrocytes (Kopen, G. C., Prockop, D. J., & Phinney, D. G. (1999). Proceedings of the National Academy of Sciences, 96, 10711-10716), but there is no definite evidence as to what functions the differentiated cells perform in vivo. It seems that the favorable effect of MSCs is induced by paracrine mechanisms rather than cell replacement, and therefore, the transplantation of MSCs would have temporary and limited effects but not the alleviation maintained for a long period of time (Cho, S. R., Kim, Y. R., Kang, H. S., et al. (2009). Cell Transplantation, 18, 1359-1368).
In contrast, embryonic stem cells (ESCs) may differentiate into all particular cell types derived from three embryonic germ layers, and have a strong self-renewal ability. Noticeably, neural precursor cells (NPCs) derived from ESCs, first, differentiate into a particular cell type of neural lineage cells including neural cells, astrocytes, and oligodendrocyte, and thus are considered to be a cell source for repair of brain tissues. These cells secrete some factors for promoting the survival and proliferation of endogenous neural precursor cells (Capone, C., Frigerio, S., Fumagalli, S., et al. (2007). PLoS One, 7, e373). However, it has not yet been known how NPCs differentiated from ESCs or the culture liquid of NPCs contribute to the improvement of functions after transplantation in disease models Throughout the entire specification, many papers and patent documents are referenced and their citations are represented.
The disclosure of the cited papers and patent documents are entirely incorporated by reference into the present specification, and the level of the technical field within which the present invention falls and the details of the present invention are explained more clearly.
The present inventors endeavored to develop a fundamental method for treating ischemic disease or neuroinflammatory disease. As a result, the present inventors found, when neural progenitor cells expressing PSA-NCAM, which is a nerve adhesibe molecule on the cell surface, are injected into the lesion site, neuroregeneration is enhanced, vascularization is promoted and the inflammatory reaction is suppressed, so that ischemic diseases caused by vascular damage and nerve tissue damage from inflammation are treated efficiently, thereby completing the present invention. In addition, as an approach different from stem cell transplantation, it is possible to reduce the ischemic injury area and restore the nerve function by administering to the lesion site of the neuroepithelial cell secretory proteins (secretome), thereby regaining the lost function in neuroinflammatory or neurodegenerative diseases such as ischemic diseases and inflammation, Thereby confirming that the disease can be effectively treated, thereby completing the present invention.
Accordingly, an aspect of the present invention is to provide a composition for treating ischemic disease or neuroinflammatory disease.
Another aspect of the present invention is to provide a method for treating ischemic disease or neuroinflammatory disease.
Other purposes and advantages of the present invention will become more obvious with the following detailed description of the invention, claims, and drawings.
In accordance with an aspect of the present invention, there is provided a composition for treating ischemic disease or neuroinflammatory disease, the composition containing poly-sialylated neural cell adhesion molecule (PSA-NCAM)-positive neural precursor cells as an active ingredient.
In accordance with another aspect of the present invention, there is provided a method for treating ischemic disease or neuroinflammatory disease, the method comprising administering a composition containing poly-sialylated neural cell adhesion molecule (PSA-NCAM)-positive neural precursor cells as an active ingredient to a subject in need thereof.
According to the present invention, the composition of the present invention restores blood vessels of ischemic tissues or inhibits inflammatory responses in a subject with ischemic disease or neuroinflammatory disease, and thus, suppresses the development of symptoms of the diseases, or removes or relieves the diseases. Therefore, the composition of the present invention per se may be a composition for treating ischemic disease or neuroinflammatory disease, or may be applied as a treatment adjuvant for the diseases when administered with other anti-ischemic/anti-inflammatory compositions. As used herein, the term “treatment” or “treatment agent” includes a meaning of “treatment aid” or “treatment adjuvant”.
According to the present invention, the composition of the present invention significantly increases an angiogenesis-inducing factor, angiopoietin-1, and greatly increases the number of blood vessels and the concentration in microvessels at sites of administration (or transplantation). Therefore, the composition of the present invention can be used as a composition for efficiently treating ischemic disease, wherein the composition restores blood vessel tissues or increases the number of blood vessels in a subject having a reduced blood flow rate caused by the loss of blood vessel tissues, deficiency of angiogenesis, or formation of abnormal blood vessels, thereby restoring the blood flow rate.
According to the present invention, the composition of the present invention inhibits the activation of reactive microglial cells and astrocytes in administered (or transplanted) neural tissues. Microglial cells perform a primary immune function in the central nervous system, and the activated microglial cells, unlike microglial cells in a normal state, perform active phagocytosis and cell proliferation, and generate inflammation-mediated materials through the expression of genes, such as cytokines (e.g., TNF-α, IL-1R, and IL-6), chemokines, inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2). Activated astrocytes also secrete inflammatory cytokines, such as IL-6, TGF-β, LIF, or IL-1, and the secreted cytokines again activate microglial cells and astrocytes, thereby aggravating environments in tissues. Therefore, the composition of the present invention, which inhibits the activation of microglial cells and astrocytes, can effectively block the damage of neural tissues due to inflammatory responses.
According to an embodiment of the present invention, the composition of the present invention increases the expression of angiopoietin-1.
As used herein, the term “increasing expression” refers to significantly increasing the expression of a gene or a protein so as to be measurable, compared with normal persons, and more specifically, the term refers to being an expression level of 130% or more compared with controls.
According to an embodiment of the present invention, the composition of the present invention inhibits the activation of glial cells or astrocytes.
As used herein, the term “inhibiting activation” refers to an in vivo transformation that causes deteriorations in the number, functions, and activation of glial cells or astrocytes, and for example, refers to significantly decreasing the expression of a specific marker (e.g., CD68 or GFAP) of those cells, being impossible to detect the expression, or making the expression an insignificant level.
According to an embodiment of the present invention, the PSA-NCAM-positive neural precursor cells are separated from neural rosettes differentiated from pluripotent stem cells.
According to the present invention, the PSA-NCAM-positive neural precursor cells may be separated from neural rosettes, which are differentiated from pluripotent stem cells through the stimulation of neural differentiation, using anti-PSA-NCAM-antibody.
In accordance with another aspect of the present invention, there is provided a composition for treating ischemic disease or neuroinflammatory disease, the composition containing, as an active ingredient, a secretome of neural precursor cells.
In accordance with another aspect of the present invention, there is provided a method for treating ischemic disease or neuroinflammatory disease, the method comprising administering a composition containing, as an active ingredient, a secretome of neural precursor cells to a subject in need thereof.
As used herein, the term “secretome of neural precursor cells” refers to an aggregate of proteins secreted from neural precursor cells to the outside (culture medium) when the neural precursor cells are cultured.
According to an embodiment of the present invention, the neural precursor cells used in the preparation of the secretome of the present invention are differentiated from pluripotent stem cells.
Acceding to an embodiment of the present invention, the neural precursor cells are neural precursor cells at the stage of neural rosettes formed by the differentiation of pluripotent stem cells (e.g., embryonic stem cells or induced pluripotent stem cells) into neural lineage cells.
According to an embodiment of the present invention, the neural precursor cells are PSA-NCAM-positive neural precursor cells.
According to another embodiment of the present invention, the neural precursor cells are PSA-NCAM-negative neural precursor cells.
The PSA-NCAM-positive or negative neural precursor cells may be separated from neural rosettes, which are differentiated from pluripotent stem cells through stimulation of neural differentiation, using anti-PSA-NCAM-antibody.
According to an embodiment, the secretome is in a form of being contained in a cell culture liquid obtained by culturing neural precursor cells in an animal cell culture medium. That is, the composition of the present invention may be contained in a culture liquid of neural precursor cells, containing a secretome of neural precursor cells.
According to an embodiment of the present invention, the cell culture liquid of the neural precursor cells may be obtained by culturing the neural precursor cells in a serum-free animal cell culture medium containing insulin/transferrin/selenium (ITS) and basic fibroblast growth factor (bFGT) and then removing the cells. For the culturing, neural precursor cells that are obtained by subculturing (e.g., at least four passages) the neural precursor cells in a bFGF-containing animal cell culture medium supplemented with, for example, N2, B-27, and/or Gem21.
The removal of the cells from the culture medium may be conducted by using an ordinary cell separation method, such as centrifugation or filtration.
For the animal cell culture medium, an ordinary medium that is used for culturing neural precursor cells may be used without limitation. For example, DMEM/F12, DMEM or RPMI-1640 may be used.
According to an embodiment of the present invention, the neural precursor cells are differentiated from human induced pluripotent stem cells, and the secretome of neural precursor cells include the following proteins:
Agrin, annexin A5, BSG (Basigin), biglycan, calponin-3, coactosin-like protein, cofilin-1, collagen alpha-2, cullin-3, destrin, dystroglycan, ephrin-B2, exportin-2, ezrin, fibronectin, fibulin-1, frizzled-related protein, gelatin-3 binding protein, granulins, growth/differentiation factor 11, haptoglobin, hemopexin, high mobility group protein B2, hornerin, importin-9, insulin-like growth factor-binding protein 2, Lupus La protein, macrophage migration inhibitory factor, midkine, moesin, neuropilin 2, pleiotrophin, profilin-1, protein DJ-1, radixin, secreted frizzled-related protein-2, septin-11, talin-1, testican, thymopoietin, transgelin-3 and vimentin.
According to an embodiment of the present invention, the neural precursor cells are differentiated from human embryonic stem cells, and the secretome of neural precursor cells include the following proteins:
Agrin, annexin A2, attractin, biglycan, ceruloplasmin, cofilin-1, collagen alpha-1, coronin-1X, dermicidin, DERP12, eprin-B3, exostosin-2, ezrin, gelatin-3 binding protein, granulins, growth/differentiation factor 11, haptoglobin, hemopexin, high mobility group protein B2, hornerin, insulin-like growth factor-binding protein 2, Lupus La protein, midkine, moesin, multiple epidermal growth factor-like domains protein 8, nidogen-1, parathymosin, profilin-2, protein DJ-1, secreted frizzled-related protein-2, secretogranin, talin-1, thymosin beta-4, TGFBI (Transforming growth factor-beta-induced protein ig-h3), transgelin and vimentin.
Hereinafter, the common contents of the composition and the treatment method of the present invention are described.
As used herein, the term “stem cells” is a generic term for undifferentiated cells before differentiation into respective cells constituting tissues, and the stem cells have an ability to be differentiated into particular cells by particular differentiation stimulations (environment). Unlike cell division-ceased undifferentiated cells, the stem cells are capable of producing the same cells as their own through cell division (self-renewal), and have plasticity in differentiation, in which the stem cells are differentiated into particular cells by the application of the differentiation stimulation and may be differentiated into various cells by different environments or by different differentiation.
The stem cells used in the present invention are pluripotent stem cells that proliferate indefinitely in vitro and can be differentiated into various cells derived from all embryonic layers (ectoderm, mesoderm, and endoderm). More specifically, the pluripotent stem cells are embryonic stem cells, induced pluripotent stem cells (iPSCs), embryonic germ cells, or embryonic carcinoma cells.
The embryonic stem cells are derived from the inner cell mass (ICM) of the blastocyst, and the embryonic germ cells are derived from primordial germ cells present in 5-10 week-old gonadal ridges.
Induced pluripotent stem cells (iPSCs) are one type of pluripotent stem cells artificially derived from non-pluripotent cells (e.g., somatic cells) by inserting a particular gene imparting pluripotency therein. Induced pluripotent stem cells are considered to be the same as pluripotent stem cells (e.g., embryonic stem cells) since the induced pluripotent stem cells have highly similar stem cell genes and protein expression, chromosomal methylation pattern, doubling time, embryoid body formation capacity, teratoma formation capacity, viable chimera formation capacity, hybridizability, and differention ability as embryonic stem cells.
The term “neural rosettes” refers to neural stems cell at the initial stage in the neural differentiation procedure of human embryonic stem cells, and the neural rosette has a cylindrical radial form. The neural rosettes are composed of cells expressing initial neuroectodermal markers, such as Pax6 and Sox1, and may be differentiated into various neural cells and neuroglial cells. The stimulation of neural differentiation may be differentiated by a method that is ordinarily conducted in the art, for example, serum-free media (Tropepe V et al., Neuron. 30:6578 (2001)), fibroblast growth factors (FGFs), and treatment with morphogens, such as Wnt and retinoic acid (RA) (Ying Q L et al. Nat Biotechnol. 21:183186 (2003)), but is not limited thereto.
Polyclonal antibodies or monoclonal antibodies may be used as the antibody. The antibodies against PSA-NCAM may be produced by the methods that are conventionally conducted in the art, for example, a fusion method (Kohler and Milstein, European Journal of Immunology, 6:511-519 (1976)), a recombinant DNA method (U.S. Pat. No. 4,816,56), or a phage antibody library method (Clackson et al, Nature, 352:624-628 (1991) and Marks et al, J. Mol. Biol., 222:58, 1-597 (1991)). A general procedure for antibody production is described in detail in Harlow, E. and Lane, D., Using Antibodies: A Laboratory Manual, Cold Spring Harbor Press, New York, 1999; Zola, H., Monoclonal Antibodies: A Manual of Techniques, CRC Press, Inc., Boca Raton, Fla., 1984; and Coligan, CURRENT PROTOCOLS IN IMMUNOLOGY, Wiley/Greene, N Y, 1991, the disclosure of which are incorporated herein by reference.
For example, hybridoma cells producing monoclonal antibodies may be obtained by fusing immortal cell lines to antibody-producing lymphocytes, the technology for which has been well known to those skilled in the art, and can be easily conducted. The polyclonal antibodies may be obtained by injecting PSA-NCAM antigens into an appropriate animal, collecting antisera from the animal, and then isolating antibodies from the antisera using the known affinity technique.
As used herein to recite the PSA-NCAM, the term “antibody” refers to a an antibody specific to PSA-NCAM, and the antibody specifically binds to the PSA-NCAM protein, and includes a complete form of an antibody and an antigen binding fragment of the antibody molecule. The complete antibody has a structure having two full-length light chains and two full-length heavy chains, and the light chains are linked to the heavy chains via a disulfide linkage, respectively. The antigen-binding fragment of the antibody molecule is a fragment having an antigen binding function, and includes Fab, F(ab′), F(ab′)2, and Fv.
For the separation of PSA-NCAM-positive neural precursor cells using an antibody, fluorescence-activating cell sorters (FACS), magnetic activated cell sorter (MACS), antibody-coated plastic adherence, and complement-mediated lysis may be used.
As used herein, the term “treatment” refers to: (a) suppressing the development of disease, disorder, or symptom; (b) reducing disease, disorder, or symptom; or (c) removing the symptoms of disease, disorder, or symptom. The composition of the present invention suppresses the development of symptoms of ischemic disease or neuroinflammatory disease, or removes or reduces the symptoms of ischemic disease or neuroinflammatory disease. Therefore, the composition of the present invention per se may be a composition for treating ischemic disease or neuroinflammatory disease, or may be applied as a treatment adjuvant for the diseases when administered with other anti-ischemic/anti-inflammatory compositions. As used herein, the term “treatment” or “treatment agent” includes a meaning of “treatment aid” or “therapeutic adjuvant”.
As used herein, the term “ischemic disease” refers to a disease of tissue necrosis through a reduction in the blood flow rate and a blockage of blood supply, caused by blood leakage, embolism, or infarction due to injuries of blood vessels.
According to an embodiment of the present invention, the ischemic disease that can be treated by the composition of the present invention is selected from the group consisting of ischemic heart disease, myocardial infarction, angina pectoris, lower limb artery ischemic disease, distal limb ischemic disease, and cerebrovascular ischemic disease.
As used herein, the term “ischemic heart disease” refers to a disease caused by the reduction in blood flow into heart muscle due to the damage, narrowness, and occlusion of coronary arteries for supplying blood to the heart. More specifically, the ischemic heart disease that can be treated by the composition of the present invention is selected from the group consisting of angina, myocardial infarction, and cardiac failure.
As used herein, the term “ischemic cerebrovascular disease” refers to a disease of the damage of brain tissues caused by the non-supply of blood flow due to the damage, narrowness, or occlusion of the brain blood vessels. More specifically, the ischemic cerebrovascular disease is ischemic stroke.
As used herein, the term “neuroinflammatory disease” refers to a disease caused by the damage of neural tissues due to inflammatory responses.
According to an embodiment of the present invention, the neuroinflammatory disease that can be treated by the composition of the present invention is selected from the group consisting of Alzheimer's disease, Parkinson's disease, Huntington's disease, Lou Gehrig's disease, Creutzfeldt Jakob disease, multiple sclerosis, amyotrophic lateral sclerosis, diffuse Lewy body disease, leukencephalitis, temporal lobe epilepsy, and inflammatory spinal cord injury.
As used herein, the term “administration” or “administer” refers to a method wherein a therapeutically effective amount of the composition of the present invention is directly administered to a subject to form the same amount thereof in the body of the subject. Therefore, the term “administer” includes the injection of an active ingredient (a secretome of PSA-NCAM-positive neural precursor cells or neural precursor cells) around a site of lesion, and thus the term “administer” is used in the same meaning as the term “inject”.
The term “therapeutically effective amount” of the composition refers to the content of an extract, which is sufficient to provide a therapeutic or prophylactic effect to a subject to be administered, and thus the term has a meaning including “prophylactically effective amount”. As used herein, the term “subject” includes, but is not limited to, human, mouse, rat, guinea pig, dog, cat, horse, cow, pig, monkey, chimpanzee, beaver, or rhesus monkey. Specifically, the subject of the present invention is human.
In cases where the composition of the present invention is prepared as a pharmaceutical composition, the pharmaceutical composition of the present invention contains a pharmaceutically acceptable carrier. The pharmaceutically acceptable carrier contained in the pharmaceutical composition of the present invention is one that is conventionally used in the formulation, and examples thereof may include, but are not limited to, lactose, dextrose, sucrose, sorbitol, mannitol, starch, acacia gum, calcium phosphate, alginate, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water, syrup, methyl cellulose, methyl hydroxybenzoate, propyl hydroxybenzoate, talc, magnesium stearate, mineral oil, saline, phosphate buffered saline (PBS), and media.
The pharmaceutical composition of the present invention may further contain, in addition to the above ingredients, a lubricant, a wetting agent, a sweetening agent, a flavoring agent, an emulsifier, a suspending agent, a preservative, and the like. Suitable pharmaceutically acceptable carriers and preparations are described in detail in Remington's Pharmaceutical Sciences (19th ed., 1995).
The pharmaceutical composition of the present invention may be administered orally or parenterally, and examples of parenteral administration may include intramuscular administration, intracerebroventricular administration, intrathecal administration, or intravascular administration.
A suitable dose of the pharmaceutical composition of the present invention may vary depending on various factors, such as the method for formulation, the manner of administration, the age, body weight, gender, morbidity, and diet of the patient, time of administration, route of administration, excretion rate, and response sensitivity. The general dose of the pharmaceutical composition of the present invention is 102-1010 cells per day on the basis of an adult.
The pharmaceutical composition of the present invention may be formulated into a unit dosage form or may be prepared in a multi-dose container by using a pharmaceutically acceptable carrier and/or excipient according to the method easily conducted by a person having an ordinary skill in the art to which the present invention pertains. Here, the dosage form may be a solution in an oily or aqueous medium, a suspension, a syrup, or an emulsion, an extract, a pulvis, a powder, a granule, a tablet, or a capsule, and may further include a dispersant or a stabilizer.
Features and advantages of the present invention are summarized as follows:
(a) The present invention provides a composition for treating ischemic diseases or neuroinflammatory diseases.
(b) PSA-NCAM-positive neural progenitor cells used in the present invention promote angiogenesis in injected tissue and inhibit an inflammatory response. The PSA-NCAM-positive neural progenitor cells can be simply isolated by using an anti-PSA-NCAM-antibody, and exhibit excellent angiogenic and anti-inflammatory activities compared with mesenchymal stem cells, and thus can be useful as a composition for effectively treating ischemic diseases caused by a vascular injury and nerve damage diseases caused by inflammation.
(c) In addition, a secretome of the neural progenitor cells of the present invention reduces the ischemic injury site and allows a neurological function to recover, and thus can be used as an agent for treating ischemic diseases and degenerative nervous system disorders such as nerve damage diseases caused by inflammation.
Hereinafter, the present invention will be described in detail with reference to examples. These examples are only for illustrating the present invention more specifically, and it will be apparent to those skilled in the art that the scope of the present invention is not limited by these examples.
Methods
Culture and Differentiation of Human MSCs and Human ESC-Derived NPCPSA-NCA+
The use of human cells was approved by the Institutional Review Board (IRB No. 4-2008-0643). Human bone marrow was obtained by aspiration from the posterior iliac crest from healthy adult volunteers who provided informed consent. Briefly, bone marrow mononuclear cells were isolated using density gradient centrifugation (GE Healthcare, Uppsala, Sweden) and were plated at a density of 1×106 cells/cm2 in DMEM supplemented with 10% FBS (Gibco, Grand Island, N.Y.), and cultured at 37° C. in a humidified atmosphere containing 5% CO2. After 24 h, non-adherent cells were washed and removed. The medium was changed every 3rd day and the cells were sub-cultured using 0.05% trypsin/EDTA (Invitrogen, Carlsbad, Calif.) when they reached 90% confluence.
Adherent MSCs at passages 3-5 were used for this study. For neural induction, embryoid bodies (EBs) derived from hESCs were cultured for 4 days in suspension with 5 μM dorsomorphin (DM) (Sigma, St. Louis, Mo.) and 5-10 μM SB431542 (SB) (Calbiochem, San Diego, Calif.) in hESC medium deprived of bFGF (Invitrogen), and then attached on Matrigel-coated dishes (BD Biosciences, Bedford, Mass.) in 1×N2 (Invitrogen) media supplemented with 20 ng/ml bFGF for the additional 5 days (Kim, D. S., Lee, D. R., Kim, H. S., et al. (2012). PLoS One, 7, e39715). Neural rosettes that appeared in the center of attached EB colonies were carefully isolated using pulled glass pipettes from the surrounding flat cells. Small rosette clumps were then seeded on Matrigel-coated dishes after gentle trituration and cultured in DMEM/F12 supplemented with 1×N2, 1×B27 (all from Invitrogen) (referred to as N2B27 medium) plus 20 ng/ml bFGF (Kim, D. S., Lee, J. S., Leem, J. W., et al. (2010). Stem Cell Reviews and Reports, 6, 270-281).
Isolation of PSA-NCAM-Positive NPCs by MACS
Expanded neural rosette cells at 80-90% confluence were exposed to 10 μM Y27632 (Sigma) for 1 h to prevent cell death prior to being subjected to MACS procedure. After dissociation using Accutase (Invitrogen), the cells (˜1×108 cells) were briefly blocked in PBS with 2% BSA, and then incubated with anti-PSANCAM antibody conjugated with microbeads (Miltenyi Biotec) for 15 min at 4° C. After extensive washing, the cell suspension was subjected to the MACS procedure and positively-labeled cells that remained in the column were eluted to a tube with culture media. Isolated NPCPSA-NCAM+ were re-plated on the culture dish at a density of 4-5×105 cells/cm2 in N2B27 medium or NBG medium plus 20 ng/ml of bFGF (1×N2, 0.5×B27, and 0.5×G21 supplement (Gemini BioProducts, West Sacramento, Calif.)). Culture medium was changed every day and the cells were passaged every 2-3 days.
Establishment of Stroke Model and Stereotaxic Injection of NPCPSA-NCAM+
The 2-month aged male Sprague-Dawley rats (approximately 250-300 g in body weight) were anesthetized with 3% isoflurane (Hana Pharm, Seoul, Korea) in a 70-30% mixture of N2O to O2. The left common carotid artery and external carotid artery were isolated and ligated with a 4-0 surgical suture. A nylon thread was inserted into the left internal carotid artery and advanced to the Circle of Willis (permanent middle cerebral artery occlusion: pMCAo). The thread was left in place until the rats were sacrificed.
Stereotaxic injection of NPCPSA-NCAM+, MSCs, or PBS was performed 2 days after pMCAo. Rats were anesthetized with zoletil (Virbac S.A., France, 25 mg/kg) and then placed in a stereotaxic surgical apparatus (David Kopf Instruments, Tujunga, Calif.). A 26-gauge needle (Hamilton syringe, Hamilton, Reno, Nev.) was inserted into the left striatum (coordinates from the bregma: anteroposterior +0.7 mm, mediolateral −2 mm and dorsoventral −5.5 mm, −2.5 mm from meninges); 5 μl of NPCPSA-NCAM+ or MSCs (1×105 cells/μl each) or PBS was injected into the 5.5 mm and −2.5 mm sites. All cells were constantly infused into the left striatum at a rate of 1 μl/min with continuous agitation to prevent cellular aggregation. Nine animals died while pMCAo surgery and cell transplantation were performed.
All animals were housed in the facility approved by the Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC), using a 12 h light/dark cycle. The experiment was approved by the Institutional Review Board (IRB No. 4-2011-0087).
Behavioral Tests
Foot fault test: The foot fault test measures the accuracy of forepaw placement on an equi-distant grid (60×60 cm, 6 cm distance) during a 2-min testing period. This test was a modified procedure that is based on the previous study [12, 13].
Asymmetric behavior test: The modified elevated body swing test was adapted from the previous report. Rats were examined for lateral movements after elevation by their tails up to 10 cm above the surface of the testing area. The frequency of left or right swing was scored for 1 min. Asymmetric score value was calculated by the following scores; score 0—torso twist, left and right swing, score 1—asymmetric twist<30°, score 2—asymmetric twist>30°. According to the direction of torso twisting, the score was counted as either ipsilateral twist (same as infarct site) or contralateral twist (opposite of infarct site).
Beam balance test: The beam walking apparatus is composed a beam (100×5×2 cm). Motor performance was graded on a 6-point scale adapted from a previous description; score 1—balance with steady posture and paws on top of the beam, score 2—grasps side of beam and has shaky movement, score 3—one or more paws slip off beam, score 4—attempts to balance on the beam but falls off, score 5—drapes over the beam but falls off, score 6—falls off the beam with no attempt to balance.
Prehensile traction test: The prehensile portion of the test involves the rat's ability to hang onto the horizontal rope by its forepaws. The prehensile traction test was used to measure the rat's muscle strength. This test was adapted from similar tests described previously. The steel bar (2-cm diameter, 100-cm length) was placed horizontally 70 cm above the sponge rubber pad (7.5 cm thickness). The rat's forepaws were placed on the steel bar and the animal was released. The rat was allowed to hang onto the steel bar for up to 5 s. Time of falling was noted as well as whether or not rat brought the rear limb up to the bar with the following scores; score 0—the rat hangs on for 5 s and brings rear limb up, score 1—rat hangs on for 5 s and no rear limb is brought up, score 2—rat hangs on for 3-4 s, score 3—the rat hangs on for 0-2 s.
Modified neurological severity score (mNSS): The neurological severity score is a composite of motor, sensory, and reflex tests as described previously. The objective quantifications were based on the asymmetric behavior test, beam balance test, prehensile traction test, open field test (rotation frequency), and foot fault test with the following scores; score 0—no deficits, score 2—difficulty in fully extending the contralateral forelimb (3 front foot fault<10), score 4—unable to extend the contralateral forelimb (front foot fault?10), score 6-mild circling to the contralateral side (1<rotation or asymmetric twisting<5), score 8—severe circling (rotation or asymmetric twisting?5), score 10—falling to the contralateral side (prehensile traction 2).
Immunohistochemical Analysis and Quantification
The brain was fixed for 24 h in 4% paraformaldehyde and washed with PBS. For the paraffin sections, the tissues were dehydrated in a graded ethanol series and then embedded in paraffin. The paraffin-embedded brain was sectioned into 5-μm-thick layers on a microtome, deparaffinized in xylene for 10 min, and rehydrated in a graded alcohol series. Sections were treated with 10 mM citric acid for 1 h followed by the addition of 5% BSA solution containing PBS and 0.5% Triton X-100. Thereafter, the brain sections were incubated with primary antibodies to DCX (Abcam), Tuj1 (Covance), hNu (Millipore, clone 235-1), GFAP (Millipore), Ki67 (Leica Microsystems), hMito (Millipore), MAP2 (Millipore), human Nestin (Millipore, clone 10C2), or ED-1 (Abcam) (1:100) for 10-12 h at 4° C. Following the overnight incubation with the primary antibodies, the sections were washed with PBS before incubating them with a fluorescently-labeled secondary antibody, anti-rabbit IgG, for 31 h. The sections were then washed once more with PBS before being mounted with 1 μg/ml 4′,6′-diamidino-2-phenylindole (DAPI). A fluorescent microscope (Olympus IX71) was used to produce fluorescent images of the sections. In order to accurately determine the numbers of neuronal cells in the brain that reacted with specific antibodies, a blind test was utilized. Three individuals, all of whom had no previous knowledge of the experiment, were asked to count the number of ED-1+ cells and α-SMA+ vessels (with diameter of 50 μm or less) in five of the squares with 50 mm2 on a slide. An investigator then took the results of all three individuals to accurately determine the number of detected neurons.
Twenty six days after transplantation, the rats (n=10 per group) were anesthetized with zoletil (Virbac S.A., France, 25 mg/kg) and perfused with PBS and 4% paraformaldehyde in PBS (pH 7.5).
For infarct area measurement, the brain sections were stained with hematoxylin and photographed with a microscope (Zeiss, Oberkochen, Germany). The indirect lesion area, in which the intact area of the ipsilateral hemisphere was subtracted from the area of the contralatera hemisphere, was calculated. Relative infarct area was analyzed with NIH Image J program (version 1.47). It was presented as an average percentage of the indirect lesion compared with contralateral hemisphere.
Reverse Transcription-Polymerase Chain Reaction (RT-PCR)
Total RNA was isolated using Trizol reagent (Invitrogen). Standard reverse-transcription (RT) was first conducted using Transcriptase II (Invitrogen) and then, RT-PCR was performed with specific PCR primer set: Forward primer: TGTGTCCATCAGCTCCAGTTGC, Reverse primer: CGGCTACCATGCTCGAGATAGG) for angiopoietin 1 (Bioneer, Daejeon, Korea). The PCR products were run at 1.2% agarose gel and then stained with ethidium bromide to detect bands (approximate size: 400 base pairs) under UV light. Finally, the detected bands were quantified by use of NIH Image J program (version 1.47).
Statistical Analysis
The data were expressed as mean±S.E.M. Data of behavioral test and infarct area were analyzed by ANOVA and independent t-test using the Statistical Package for Social Sciences (SPSS) version 20.0. Differences with P-values<0.05 were considered to be statistically significant.
Results
Transplantation of NPCPSA-NCAM+ Reduced Infarction Area in Host Brain
The overall design for this experiment is shown in
The severity of neural tissue damage was determined as brain area which is not normally stained with hematoxylin at day 26 following transplantation. Infarct lesions mainly appeared on the cortex and striatum. Infarction area was obviously larger in ischemic brains treated with PBS than in those transplanted with MSCs or NPCPSA-NCAM+ (
Transplantation of NPCPSA-NCA+ Improved Behavioral Performances of a Rat Stroke Model
The rats lost 40 g of their body weight compared to a baseline measured on the first day after pMCAo. The weight loss reached maximum at day 7 after treatment in PBS-treated rats. In MSC-transplanted group, the body weight was recovered to baseline state by day 17 after transplantation. However, the significant recovery of body weight began to appear from day 3 after transplantation in the NPCPSA-NCAM+-transplanted group when compared with PBS controls (P<0.05) (
While all rats displayed relatively little asymmetry in EBTS before pMCAo, asymmetry was evident in all animals after pMCAo. On day 3 post-transplantation, NPCPSA-NCAM+- and MSC-transplanted groups started to show ipsilateral twisting behavior. Whereas MSC-transplanted group showed modest improvement up to day 13 after transplantation (P<0.05), the asymmetric behavior score significantly decreased in NPCPSA-NCAM+ transplanted group at day 7 and lasted up to day 24 after transplantation (P<0.01) (
NPCPSA-NCAM+ transplantation also improved functional recovery in the beam balance test from day 3 through 24, compared with MSC-transplanted group and PBS controls (P<0.01) (
Prehensile traction score, negatively related with muscle strength of the forepaw, gradually decreased in NPCPSA-NCAM+ transplanted group from day 3 through 24 (P<0.01) (
To normalize the quantifications of neurologic outcome, the present inventors finally assessed the mNSS criteria based on a asymmetric behavior score, beam balance test, prehensile traction test, open field test (rotation frequency, data not shown), and foot fault test. The mNSS showed that progressive recovery in neurological function becomes significant after day 3 in both NPCPSA-NCAM+-and MSC-transplanted groups compared to PBS-treated groups (P<0.05) (
Transplanted NPCPSA-NCA+ Survived and Differentiated into with Neuronal Commitment in Host Brain
To track destiny of transplanted cells, the present inventors performed histologic analysis with hNu (human-specific nuclei), Ki67 (proliferating cell marker), DCX (neuroblast marker), nestin (neural stem cell marker), and Tuj1 (neuronal marker) antibodies at day 26. Following transplantation of NPCPSA-NCAM+, most cells were found at the original transplantation site (i.e., striatum). The survival, proliferation, and differentiation of transplanted NPCPSA-NCAM+ were confirmed by Ki67+, DCX+, Tuj1+, and nestin+ cells in damaged brain (
Whereas many transplanted NPCPSA-NCAM+ demonstrated good survival and integration into damaged tissue, only a few MSCs were detected with hNu expression at day 26 following transplantation (
While the hMito+MAP2+ and hNu+MAP2+ double-labeled cells were detected in NPCPSA-NCAM+-transplanted rats (
Transplantation of NPCPSA-NCAM+ Suppressed Reactive Glial Activation in Host Brain
Expression of GFAP (astrocyte marker), was notably low in NPCPSA-NCAM+-transplanted group, although some GFAP positive cells were found along the needle tracks (
Ischemic stroke induces adverse microglial response accompanied by tissue damage. Thus, the present inventors examined the microglial activation in ischemic brain tissues at day 26 following transplantation using an ED1 antibody that recognizes CD68 (active microglial marker) (
Transplantation of NPCPSA-NCAM+ Enhanced Angiogenesis in Host Brain
Endogenous angiogenesis was examined in ischemic brain tissues using α-SMA antibody, a smooth muscle actin marker. As a result, it was observed that the number of α-SMA-reactive vessels in NPCPSA-NCAM+-transplanted rats increased around the graft site, compared with those of MSC- and PBS-treated groups (
When the expression levels of pro-angiogenic marker, angiopoietin-1, in the brain tissues were investigated using RT-PCR at day 7 and 26 after transplantation, the levels were substantially higher in NPCPSA-NCAM+-transplanted rats at day 26 than other groups (P<0.05) (
Materials and Methods
Human ESC-Derived NPCPSA-NCAM+ Cells
The use of human cells was approved by the Institutional Review Board (IRB No. 4-2008-0643). For neural induction, embryoid bodies (EBs) derived from hESCs and iPSC were cultured for 4 days in suspension with 5 μM dorsomorphin (DM) (Sigma, St. Louis, Mo.) and 5-10 μM SB431542 (SB) (Calbiochem, San Diego, Calif.) in hESC medium deprived of bFGF (Invitrogen), and then attached on Matrigel-coated dishes (BD Biosciences, Bedford, Mass.) in 1×N2 (Invitrogen) media supplemented with 20 ng/ml bFGF for the additional 5 days (Kim, D. S., Lee, D. R., Kim, H. S., et al. (2012). Highly pure and expandable PSA-NCAM-positive neural precursors from human ESC and iPSC-derived neural rosettes. PLoS One, 7, e39715). Neural rosettes that appeared in the center of attached EB colonies were carefully isolated using pulled glass pipettes from the surrounding flat cells. Small rosette clumps were then seeded on Matrigel-coated dishes and cultured in DMEM/F12 supplemented with 1×N2, 1×B27 (Invitrogen) (Kim, D. S., Lee, J. S., Leem, J. W., et al. (2010). Robust enhancement of neural differentiation from human ES and iPS cells regardless of their innate difference in differentiation propensity. Stem Cell Reviews and Reports, 6, 270-281).
Expanded neural rosette cells at 80-90% confluence were exposed to 10 μM Y27632 (Sigma) for 1 h to prevent cell death prior to being subjected to MACS procedure. After dissociation using Accutase (Invitrogen), the cells (1×108 cells or less) were briefly blocked in PBS with 1% BSA, and then incubated with anti-PSA-NCAM antibody conjugated with microbeads (Miltenyi Biotec) for 15 min at 4° C. After extensive washing, the cell suspension was subjected to the MACS procedure, and positively-labeled cells that remained in the column were eluted to a tube with culture media. Isolated NPCPSA-NCAM+ were re-plated on the culture dish at a density of 4 to 5×105 cells/cm2 in N2B27 medium or NBG medium plus 20 ng/ml of bFGF (1×N2, 0.5×B27, and 0.5×G21 supplement (Gemini BioProducts, West Sacramento, Calif.)). Culture medium was changed every day and the cells were passaged every 2-3 days.
Isolation of Secretome in Human Pluripotent Stem Cell-Derived Neural Precursor Cells (NPSs)
The obtained human pluripotent stem cell-neural precursor cells (PSA-NCAM-positive neural precursor cells) were repeatedly cultured and amplified for 4 passages or more in a Matrigel-coated 60-mm dish with serum removal supplements of N2 (100×—final concentration 1×), B-27 (50×—final concentration 0.5×) and Gem21 (50×—final concentration 0.5×) and bFGF (20 ng/ml) in a base culture (DMEM/F-12), and then grown in 8-10 dishes until the cells reached 90% confluence. Following removal of the culture liquid, the cells were washed three times with phosphate buffered saline, and cultured for 24 h in a serum-free base culture liquid (DMEM/F12) supplemented with only ITS (100×—final concentration 1×) and bFGF (20 ng/ml). For a control, the same amount of base culture liquid with the same composition (base culture liquid supplemented with the same amount of ITS and bFGF) was put in a dish without cells, and cultured in an incubator for 24 h, and then collected. The culture liquid was all collected and centrifuged (800 g at 30 min) to remove cellular debris, and then directly frozen in a freezer at −70° C., and, when necessary, was thawed before use.
Establishment of Stroke Model
In order to measure the neural protective effects against neural damage due to local ischemic stroke, an applied intraluminal suture method was used. This method is a local ischemic stroke model developed by Zia Longa (Zea Longa, et al, Stroke, 1989, 20, 84-91), and an advantage of clinical similarity, unlike other models. For this reason, this model is suitable to search for ischemia-reperfusion mechanism or the screening of effects of several drugs.
After acclimatization for one week, animals (male Sprague-Dawley rat, body weight 250-300 g) were anesthetized using a respiration anesthetic machine, and isoflurane was used for an anesthetic drug. White rats were first subjected to general anesthesia using a mixture gas of 80% N2O and 20% O2, and 5% isoflurane, which was then maintained at 2-2.5% for anesthesia. For the establishment of stroke model, the left neck skin of the white rats was incised, and then the common carotid artery, external carotid artery, and internal carotid artery were isolated, and the respective arteries were slightly tied with a black silk thread to block the blood flow. The common carotid artery was cut in half, and the 25-mm 4-0 nylon probe with an end of 0.40 mm, obtained by rounding the end of the nylon suture using cautery, was inserted through the cut section. The nylon probe inserted into the external carotid artery was inserted and fixed into the middle cerebral artery via the internal carotid artery. After the probe is inserted at about 18-20 mm from the branch site of the common carotid artery, the origin of the middle cerebral artery was blocked, and then fixed by a thread to permanently occlude the middle cerebral artery. Thereafter, the skin incision site was again sutured, and then the rats were naturally recovered from the anesthesia.
Injection of Secretome into Stroke Model Through Cerebral Artery and Behavioral Test
After the baseline for the behavioral test was established one day after stroke induction, an insulin syringe needle is inserted into the internal carotid artery via the right external carotid artery in the same manner as stroke model establishment, and through the needle, 0.2 mg/kg (volume 50 μl) of the secretome was intraarterially injected, and the same volume of the culture liquid or phosphate buffered saline (PBS) was administered as a control. After the injection of the secretome liquid, the state of the animals was observed for 14 days. The weight measurement was conducted once before injection and four times after injection, and the behavioral analysis was conducted.
1) Torso twisting test: In order to test the upper body posture considered as the sense of the cerebral cortex and striatum of animals, asymmetric behavior was measured.
2) Beam balance test: The gross vestibulomotor function was evaluated through steady posture of the animals on the narrow beam.
3) Foot-fault test: This test is used when the adjustment (cooperation) and unification (integration) of the motor movement are tested. The foot fault is defined that the paw falls between the grid bars or the rat misplaces a forelimb or hind-limb. The foot fault is symmetric in normal animals.
4) Prehensile Traction test: The prehensile portion of the test involves the rat's ability to hang onto the horizontal rope by its forepaws. The prehensile traction test was used to measure the rat's muscle strength. This test was adapted from similar tests described previously. The steel bar (2-cm diameter, 100-cm length) was placed horizontally 70 cm above the sponge rubber pad (7.5 cm thickness). The rat's forepaws were placed on the steel bar and the animal was released. The animals were allowed to hang onto the steel bar for up to 5 s. Time of falling was noted as well as whether or not the animals brought the rear limb up to the bar with the following scores; score 0—the rat hangs on for 5 s and brings rear limb up, score 1—rat hangs on for 5 s and no rear limb is brought up, score 2—rat hangs on for 3-4 s, score 3—the rat hangs on for 0-2 s.
5) Open-field test: This test is used to find out general walking activity levels. The activity, emotion, and behavioral patterns of the animals were measured by directly measuring the behavioral aspects and characteristics.
6) Modified Neural Severity Score (mNSS): The score is a total score of motor, sensory, balance, reaction, and emotion test values obtained through the above various tests, and the score is calculated by the following criteria (mNSS is measured by adding up scores for each subject).
Open Field Test (Measuring Emotion, Activity, and Behavioral Patterns of Animals).
No movement: 3
1-20: 2
21-30: 1
30 or more: 0
Prehensile Traction Test (Muscular Measurement)
0-5 s: 3
6-10 s: 2
11-20 s: 1
21 s or over: 0
Beam Balance Test (Measurement of Sense of Balance)
Score 0: 1=Stable posture
Score 1: 3=one or more paws slip off beam.
Score 2: 5=drapes over the beam but falls off.
Foot Fault Test (Motor Cooperation Ability)
0-5 s: 0
6-10 s: 1
11-20 s: 2
21 s or above: 3
Upper Body Posture Test (Asymmetric Behavior Test)
0: 2
1-4: 1
5 or more: 0
The white rats were anesthetized with zoletil 14 days after ischemic induction, and subjected to lung open and right auricle incision. A needle was injected into the left ventricle, and then, the heart was perfused with PBS using a pump to remove blood flow, and then the brain tissue was extracted. The tissue sections for sample construction were embedded in paraffin on the basis of bregma. For verification of damaged brain tissue, the brain tissue sections were stained with haematoxylin and dehydrated, and the slide was photographed using a digital camera, and then transferred to a computer. The percentage of infarction area was calculated by equation 1 using an image analysis program (image J).
Percentage of infarct (%)=(the area of the contralateral hemisphere−the intact area of the ipsilateral hemisphere)/the area of the contralateral hemisphere×100 Equation 1
Secretomics
The secretome of neural precursor cells derived from hESC and the secretome of neural precursor cells derived from human iPSC were separated on SDS-PAGE using 4-12% gradient Novex Bis-Tris gel (Invitrogen), and then gels were stained with Gel Code Blue staining reagent (Piece) to show protein bands. The stained gels were cut into 10 bands with the same size, which were then subjected to In-Gel Tryptic Digestion by a known method.
The peptides prepared by the In-gel tryptic digestion were analyzed by the LinearTrap Quadrupole (LTQ) mass spectrometer (Thermo Finnigan) coupled with Nano Ultra Performance liquid chromatography (Eksigent Technologies). Specifically, trypsinized peptides were applied to an analytical column (75 μm×11 cm) packed with C18 regular 5 μm-sized resin. A linear 45 min gradient was achieved from 97% solvent A (0.1% formic acid in distilled water) to 60% solvent B (0.1% formic acid in acetonitrile) at a flow rate of 0.3 μl/min. The separated peptide ions were electrosprayed into the nano-electrospray ionisation (ESI) source. All MS/MS spectra were acquired by data-dependent scans in which the five most abundant spectra from the full MS scan were selected for fragmentation. The repeat count for dynamic exclusion was set to 1, the repeat duration was 30 s, the dynamic exclusion duration was set to 180 s, the exclusion mass width was 1.5 Da, and the list of dynamic exclusion was 50.
The identification of peptides and proteins was researched from ipi.HUMAN v3.76 database (89 378 entries) using Turbo-SEQUEST algorithm (Thermo Finnigan). Following database research, the identified peptides and proteins were confirmed using scaffold 2 (Proteome Software). Among the peptides obtained from the SEQUEST search, a set of peptides with a PeptideProphet probability greater than 0.95 was selected. Furthermore, a list of proteins that had a ProteinProphet probability greater than 0.99 and also had more than two unique peptides obtained.
Statistical Analysis
The statistical significance among groups was obtained using one-way analysis of variance (ANOVA) with Tukey's correction, and a p value<0.05 was determined to be statistically significant.
Results
To investigate the alleviation of the disease by the secretome of neural precursor cells in a stoke model, the following three groups were tested for 2 weeks. At 24 h after stroke induction, white rats with the induced disease confirmed by behavior test were arbitrarily allocated into three groups, and an equal volume (50 μl) of the secretome (0.2 mg/kg, volume 50 μl), medium, or PBS was injected into the right external carotid artery. The condition and weight of animals were monitored at 3, 7, 10, and 14 after the injection of each material, and behavior analysis was performed.
Ischemic Lesion Analysis Results
The induction of stroke through permanent MCAO in white rats induced extensive brain lesion. The brain was extracted 14 days after the stroke induction, and then the damage and the damaged sites of the brain were confirmed by TTC (2,3,5-triphenyltetrazolium chloride) staining. TTC staining occurs by a reaction with normal mitochondrial oxidative enzyme system in cells, and the damaged mitochondria by ischemic damage are not stained due to the disturbance of the oxidative system, showing white, which can differentiate the damaged sites of the brain.
As shown in
Body Weight Analysis Results
The stroke induction reduces the motor performance of white rats, the immediate weight loss was advanced by 7 days, and various treatment agents induced the body weight increase through the recovery of motor performance. The injection of the secretome also induced the body weight increase similar to cell transplantation (
Behavior Analysis Results
The secretome-treated group showed a statistically significant behavior improvement effect compared with the two controls in the beam balance test, and there was an immediate effect, for example, the effect was exhibited from day 3 post-treatment (
In addition, the secretome-treated group showed a statistically significant effect compared with the two controls on day 7 post-treatment (injection) in the prehensile traction test.
Further, the injection of the secretome showed the reduction effect in the foot fault frequency in a net (
Modified Neurological Severity Score (mNSS) Analysis Results
The modified neurological severity score (mNSS) test is a composite table for measuring neurological functions. Motor (muscle state) and sensory (vision, touch, and proproceptive) items were evaluated. Normal score is 0, and the higher score, the more severe is the dysfunctions. As shown in
In the mNSS test, the PBS control showed that the average score was 5.4 n day 1 and 5.5 on day 14 after the ischemic induction, indicating that the neurobehavioral disorders caused by stroke was maintained. The medium control showed a temporary behavior improvement effect on day 3 of treatment, but did not exert an additional improvement effect. Whereas, the secretome-treated group showed a continuous behavior improvement effect from day 3 of treatment (mNSS score: 4.5) to day 10 of treatment (mNSS score: 3).
Secretome Analysis Results
The secretome obtained from neural precursor cells derived from iPSCs includes the following proteins: Agrin, annexin A5, BSG (Basigin), biglycan, calponin-3, coactosin-like protein, cofilin-1, collagen alpha-2, cullin-3, destrin, dystroglycan, ephrin-B2, exportin-2, ezrin, fibronectin, fibulin-1, frizzled-related protein, gelatin-3 binding protein, granulins, growth/differentiation factor 11, haptoglobin, hemopexin, high mobility group protein B2, hornerin, importin-9, insulin-like growth factor-binding protein 2, Lupus La protein, macrophage migration inhibitory factor, midkine, moesin, neuropilin 2, pleiotrophin, profilin-1, protein DJ-1, radixin, secreted frizzled-related protein-2, septin-11, talin-1, testican, thymopoietin, transgelin-3 and vimentin.
The secretome obtained from neural precursor cells derived from human embryonic stem cells includes the following proteins: Agrin, annexin A2, attractin, biglycan, ceruloplasmin, cofilin-1, collagen alpha-1, coronin-1X, dermicidin, DERP12, eprin-B3, exostosin-2, ezrin, gelatin-3 binding protein, granulins, growth/differentiation factor 11, haptoglobin, hemopexin, high mobility group protein B2, hornerin, insulin-like growth factor-binding protein 2, Lupus La protein, midkine, moesin, multiple epidermal growth factor-like domains protein 8, nidogen-1, parathymosin, profilin-2, protein DJ-1, secreted frizzled-related protein-2, secretogranin, talin-1, thymosin beta-4, TGFBI (Transforming growth factor-beta-induced protein ig-h3), transgelin and vimentin.
Although the present invention has been described in detail with reference to the specific features, it will be apparent to those skilled in the art that this description is only for a preferred embodiment and does not limit the scope of the present invention. Thus, the substantial scope of the present invention will be defined by the appended claims and equivalents thereof.
This application contains references to amino acid sequences and/or nucleic acid sequences which have been submitted concurrently herewith as the sequence listing .xml file entitled “000190uscoa_SequenceListing_ST26.xml”, file size 3.69 kilobytes (KB), created on 19 Aug. 2022. The aforementioned sequence listing is hereby incorporated by reference in its entirety pursuant to 37 C.F.R. § 1.52(e)(5).
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2014-0080009 | Jun 2014 | KR | national |
This application is a continuation application of U.S. application Ser. No. 15/322,003, filed on 23 Dec. 2016, which is a national phase entry of PCT Application No. PCT/KR2015/006588, filed on 26 Jun. 2015, which claims priority to Korean Patent Application No. 10-2014-0080009, filed on 27 Jun. 2014. The entire disclosure of the applications identified in this paragraph is incorporated herein by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15322003 | Dec 2016 | US |
| Child | 17884021 | US |
