Neural progenitor cells derived from embryonic stem cells

• US 20060078543A1
• Filed: 09/29/2005
• Published: 04/13/2006
• Est. Priority Date: 03/14/2000
• Status: Abandoned Application

• Current Assignee: Benjamin Eithan Reubinoff, Martin Frederick Pera, Tamir Ben-Hur
• Original Assignee: Benjamin Eithan Reubinoff, Martin Frederick Pera, Tamir Ben-Hur
• Inventors: Ben-Hur, Tamir, Pera, Martin Frederick, Reubinoff, Benjamin Eithan
• Application Number:
  US11/238,574
• Publication Number:
  US 20060078543A1
• Time in Patent Office: Days
• US Class Current: 424/93.210
• CPC Class Codes: A61K 35/12 Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells vaccines or medicinal preparations containing antigens or antibodies A61K39/00
• CPC Class Codes: A61P 17/02 for treating wounds, ulcers, burns, scars, keloids, or the like
• CPC Class Codes: A61P 25/00 Drugs for disorders of the nervous system
• CPC Class Codes: A61P 25/28 for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• CPC Class Codes: A61P 37/00 Drugs for immunological or allergic disorders
• CPC Class Codes: A61P 43/00 Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• CPC Class Codes: A61P 9/00 Drugs for disorders of the cardiovascular system
• CPC Class Codes: C12N 2500/32 Amino acids
• CPC Class Codes: C12N 2501/11 Epidermal growth factor [EGF]
• CPC Class Codes: C12N 2501/115 Basic fibroblast growth factor (bFGF, FGF-2)
• CPC Class Codes: C12N 2501/135 Platelet-derived growth factor [PDGF]
• CPC Class Codes: C12N 2501/155 Bone morphogenic proteins [BMP]; Osteogenins; Osteogenic factor; Bone inducing factor
• CPC Class Codes: C12N 2501/385 of the family of the retinoic acid recptor, e.g. RAR, RXR; Peroxisome proliferator-activated receptor [PPAR]
• CPC Class Codes: C12N 2501/39 Steroid hormones
• CPC Class Codes: C12N 2501/91 Heparin
• CPC Class Codes: C12N 2502/13 connective tissue cells; generic mesenchyme cells, e.g. so-called "embryonic fibroblasts"
• CPC Class Codes: C12N 2506/02 from embryonic cells
• CPC Class Codes: C12N 5/0606 Pluripotent embryonic cells, e.g. embryonic stem cells [ES] embryonic germ cells C12N5/0611, induced pluripotent stem cells C12N5/0696
• CPC Class Codes: C12N 5/0619 Neurons
• CPC Class Codes: C12N 5/0622 Glial cells, e.g. astrocytes, oligodendrocytes; Schwann cells
• CPC Class Codes: C12N 5/0623 : Stem cells

Abstract

The present invention relates to undifferentiated human embryonic stem cells, methods of cultivation and propagation and production of differentiated cells. In particular it relates to the production of human ES cells capable of yielding somatic differentiated cells in vitro, as well as committed progenitor cells such as neural progenitor cells capable of giving rise to mature somatic cells including neural cells and/or glial cells and uses thereof. This invention provides methods that generate in vitro and in vivo models of controlled differentiation of ES cells towards the neural lineage. The model, and cells that are generated along the pathway of neural differentiation may be used for: the study of the cellular and molecular biology of human neural development, discovery of genes, growth factors, and differentiation factors that play a role in neural differentiation and regeneration, drug discovery and the development of screening assays for teratogenic, toxic and neuroprotective effects.

Claims

1. An enriched preparation of human undifferentiated embryonic stem cells wherein said cells are capable of proliferation in vitro and differentiation to neural progenitor cells, neuron cells and/or glial cells.

2. The enriched preparation of human undifferentiated embryonic stem cells according to claim 1 wherein said cells maintain an undifferentiated state when cultured on a fibroblast feeder layer in the absence of a differentiating signal.

3. The enriched preparation of human undifferentiated embryonic stem cells according to claim 1 or 2 wherein said cells are capable of differentiation into neural progenitor cells.

4. An undifferentiated human embryonic stem cell wherein the cell is capable of proliferation in vitro and differentiation to neural progenitor cells, neuron cells and/or glial cells and is immunoreactive with markers for human pluripotent stem cells including SSEA-4, GCTM-2 antigen, and TRA 1-60.

5. The undifferentiated human embryonic stem cell according to claim 4 wherein the cell expresses Oct-4.

6. The undifferentiated human embryonic stem cell according to claim 5 wherein said cell maintains a diploid karyotype during prolonged cultivation in vivo.

7. The undifferentiated human embryonic stem cell according to any one of claims 4 to 6 which forms tumors when injected in the testis of immunodeprived SCID mice.

8. A differentiated committed human progenitor cell line capable of differentiation and propagation into mature neurons and/or glial cells said cell line derived from undifferentiated human embryonic stem cells.

9. The differentiated committed human progenitor cell line according to claim 8 capable of establishing a graft in a recipient brain.

10. The differentiated committed human progenitor cell line according to claim 9 capable of differentiating in vivo into other cell lineages including neurons and glial cells wherein the glial cells are selected from the group including astrocytes and oligodendrocytes.

11. A neural progenitor cell differentiated in vitro from an undifferentiated human embryonic stem cell.

12. The neural progenitor cell according to claim 11 wherein said cell is capable of proliferation.

13. The neural progenitor cell according to claim 11 wherein said cell is capable of differentiating to a mature neuron cell or glial cell.

14. The neural progenitor cell according to claim 11 wherein said cell is capable of transdifferentiation into other cell lineages to generate stem cells and differentiated cells of non-neural phenotype including hemangioblast, haematopoietic stem cells, endothelial stem cells, embryonic endoderm and ectodermal cells.

15. The differentiated neural progenitor cell according claims 8 or 11 characterised by expressed markers including markers of the neuroectodermal lineage;

markers of neural progenitor cells;

neuro-filament proteins;

monoclonal antibodies including MAP2ab;

glutamate;

synaptophysin;

glutamic acid decarboxylase;

GABA, serotonin, tyrosine hydroxylase;

β

-tubulin;

β

-tubulin III;

GABA Aα

2 receptor, glial fibrillary acidic protein (GFAP), 2′

,3′

-cyclic nucleotide 3′

-phosphodiesterase (CNPase), plp, DM-20, O4 and NG-2 immunostaining.

16. The neural progenitor cell according to claim 15 which expresses markers of neuroectoderm and neural progenitor cells selected from the group including polysialylated N-CAM, N-CAM, A2B5, nestin, vimentin and the transcriptional factor Pax-6, and do not express Oct-4.

17. The neural progenitor cell according to claim 16 wherein said cell is capable of establishing a graft in a recipient brain.

18. The neural progenitor cell according to claim 17 wherein said cell can incorporate extensively into a recipient brain.

19. The neural progenitor cell according to claim 18 wherein said cell is capable of migrating along host brain pathways.

20. The neural progenitor cell according to claim 19 wherein said cell is capable of wide spread distribution in host brain.

21. The neural progenitor cell according to claim 20 wherein said cell is responsive to host environmental signals.

22. The neural progenitor cell according to claim 21 wherein said cell differentiates in response to local host environmental signals.

23. The neural progenitor cell according to claim 22 wherein said cell is capable of differentiation to progeny of neural lineages selected from the group including neurons, oligodendrocyte and astrocyte in a recipient brain.

24. The enriched preparation of neural progenitor cells including an enrichment of cells according to claim 23.

25. The enriched preparation of neural progenitor cells according to claim 24 wherein said cells are capable of prolonged undifferentiated proliferation and expansion in in vitro culture.

26. The enriched preparation of neural progenitor cells according to claim 24 wherein said cells are capable of differentiation into neurons, mature neurons and glial cells.

27. The enriched preparation of neural progenitor cells according to claim 24 wherein said cells are capable of establishing a graft in a recipient brain in the absence of tumors.

28. The enriched preparation of neural progenitor cells according to claim 25 wherein said cells may be recovered from cryopreservation.

29. A method of preparing undifferentiated human embryonic stem cells for differentiation into neural progenitor cells, said method including:

obtaining an in vitro fertilised human embryo and growing the embryo to a blastocyst stage of development;

removing inner cells mass (ICM) cells from the embryo;

culturing ICM cells under conditions which do not induce extraembryonic differentiation and cell death, and promote proliferation of undifferentiated stem cells; and

recovering the stem cells.

30. The method according to claim 29 including culturing the ICM cells on a fibroblast feeder layer to promote proliferation of embryonic stem cells prior to recovering the stem cells from the feeder layer.

31. The method according to claim 30 wherein said fibroblasts are selected from human or mouse fibroblasts or a combination of human and mouse fibroblasts.

32. The method according to claim 31 wherein the fibroblast feeder layer comprises embryonic fibroblasts.

33. The method according to claim 32 wherein said fibroblasts are derived from inbred 129/Sv or CBA mice or mice from a cross of 129/Sv with C57/B16 strains.

34. The method according to claim 30 wherein said fibroblast feeder layer has a density of approximately 25,000 human and 70,000 mouse cells per cm² or 75,000 to 100,000 mouse cells per cm².

35. The method according to claim 34 wherein the fibroblast feeder layer is established 6 to 48 hours prior to addition of ES or ICM cells.

36. The method according to claim 35 wherein the fibroblast feeder cells are arrested in their growth.

37. The method according to claim 36 wherein the fibroblast feeder cells are arrested by irradiation or treated with mitomycin C.

38. The method according to claims 29 further including:

replating the stem cells from the fibroblast feeder layer onto another fibroblast feeder layer; and

culturing the stem cells for a period sufficient to promote proliferation of morphologically undifferentiated stem cells.

39. The undifferentiated human embryonic stem cell prepared by a method according to claim 38.

60. A method of producing an enriched preparation of human ES derived neural progenitor cells, said method comprising:

obtaining an undifferentiated human embryonic stem cell according to claim 39;

inducing somatic differentiation of the embryonic stem cell to a neural progenitor cell by a method according to claim 40;

identifying a neural progenitor cell by expressed markers of primitive neuroectoderm and neural stem cells and wherein said markers are selected from the group including polysialyated N-CAM, N-CAM, A2B5, intermediate filament proteins including nestin and vimentin and the transcription factor Pax-6; and

culturing the neural progenitor cells to promote proliferation and propagation.

61. The method according to claim 60 wherein the neural progenitor cells are cultured as spheres or monolayers in serum free medium comprising DMEM/F12 supplemented with B27 and growth factors.

62. The method according to claim 61 wherein the growth factors include EGF and bFGF.

63. The method according to claim 62 including further culturing to eliminate non-neural cells, in particular extrambryonic endodermal cells, said culturing comprising further selective culturing in serum free media including DMEM/F12 supplemented with B27 and growth factors.

64. The method according to claim 63 wherein the further culturing includes the transfer of undifferentiated ES cell clumps into serum free medium comprised of DMEM/F12 supplemented with B27, bFGF and EGF and cultivation of the resulting neural progenitors as spheres or monolayers.

40. A method of inducing somatic differentiation of stem cells in vitro into progenitor cells said method comprising:

obtaining undifferentiated embryonic stem cells; and

providing a differentiating signal under conditions which are non-permissive for stem cell renewal, do not kill cells and/or induces unidirectional differentiation toward extraembryonic lineages.

41. The method according to claim 40 wherein said undifferentiated embryonic stem cell is an undifferentiated human embryonic stem cell wherein the cell is capable of proliferation in vitro and differentiation to neural progenitor cells, neuron cells and/or glial cells and is immunoreactive with markers for human pluripotent stem cells including SSEA-4, GCTM-2 antigen, and TRA 1-60.

42. The method according to claim 40 wherein the conditions for inducing somatic differentiation of stem cells are selected from any one of the following including:

culturing the undifferentiated stem cells for prolonged periods and at high density on a fibroblast feeder cell layer to induce differentiation;

culturing the undifferentiated stem cells in serum free media;

culturing the undifferentiated stem cells on a differentiation inducing fibroblast feeder layer and wherein said fibroblast feeder layer does not induce extra embryonic differentiation and cell death;

culturing to a high density in monolayer or on semi-permeable membranes so as to create structures mimicing the postimplantation phase of human development;

or

culturing in the presence of a chemical differentiation factor selected from the group including bone morphogenic protein-2 or antagonists thereof.

43. A differentiated progenitor cell prepared by the method according to any one of claims 40 to 42.

44. The differentiated progenitor cell according to claim 43 selected from the group consisting of a neural progenitor cell, mesodermal progenitor cell including hemangioblast, hematopoietic or endothelial stem cells, endodermal and ectodermal progenitors.

45. The differentiated progenitor cell according to claim 44 which is a neural progenitor cell capable of differentiating into a neuron cell and/or a glial cell.

65. A method of transplanting ES derived neural progenitor cells in a host, said method comprising:

obtaining a source of neural progenitor cells prepared by a method according to claims 40;

culturing the neural progenitor cells in the presence of serum free medium supplemented with B27 and growth factors including, EGF and bFGF; and

injecting the neural progenitor cells into the nervous system of the host.

66. The method according to claim 65 wherein the neural progenitor cells are injected into the lateral cerebral ventricle of the nervous system.

67. A method of producing a stable graft of neural cells and contributing in the histogenesis of a living host said method comprising:

transplanting ES derived neural progenitor cells into a living host by a method according to claim 66.

68. A method of modifying a nervous system of a host, said method comprising transplanting ES derived neural progenitor cells by a method according to claims 67.

69. The method according to claim 68 wherein said modifying of the nervous system includes any one of replacing deficient neuronal or glial cell populations, restoring deficient functions or activating regenerative and healing processes in the nervous system to regenerate cell populations.

70. The method according to claim 68 wherein the neural progenitor cells comprise genetically modified neural progenitor cells.

71. The method according to claim 70 wherein the genetically modified neural progenitor cells express specific desired genes at the target organ.

72. A method for treating a pathological condition of the nervous system comprising modifying a nervous system of a patient according to claims 68.

73. The method according to claim 72 wherein the pathological condition is selected from the group including neurodegenerative disorders, mental disorders, vascular conditions, autoimmune disorders, congenital disorders, and trauma.

46. A method of inducing somatic cells from embryonic stem cell derived somatic progenitors, said method comprising:

obtaining a source of embryonic stem cell derived somatic progenitors;

culturing the progenitor cells on an adhesive substrate; and

inducing the cells to differentiate to somatic cells under conditions which favour somatic differentiation.

47. The method according to claim 46 wherein said embryonic stem cell derived somatic progenitor cells are grown in the presence of a serum free media and growth factors and are induced to differentiate by withdrawal of the growth factors.

48. The method according to claim 46 wherein the embryonic stem cell-derived progenitor cell is a cell selected from the group consisting of a neural progenitor cell, mesodermal progenitor cell including hemangioblast, hematopoietic or endothelial stem cells, endodermal and ectodermal progenitors.

49. The method according to claim 46 wherein the progenitor cells are cultured on an adhesive substrate selected from poly-D-lysine and laminin or poly-D-lysine and fibronectin.

50. The method according to claim 49 wherein the progenitor cells are cultured on poly-D-lysine and laminin.

51. The method according to claim 50 wherein the cells are further cultured in the presence of retinoic acid.

52. The method according to claim 47 wherein said somatic cells induced are neurons including mature neurons.

53. A mature neuron cell prepared by the method according to claim 52 and characterised by expression of the 160 kDa neurofilament protein, MAP2ab, glutamate, synaptophysin, glutamic acid decarboxylase (GAD), GABA, tyrosine hydroxylase and serotonin.

54. The method according to claim 49 wherein the progenitor cells are cultured on poly-D-lysine and fibronectin.

55. The method according to claim 54 wherein the progenitor cells are cultured before and after plating on poly-D-lysine and fibronectin in serum free medium in the presence of PDGF-AA and bFGF.

56. The method according to claim 55 wherein the progenitor cells are cultured after plating in the presence of PDGF-AA, basic FGF and EGF.

57. The method according to claim 56 further including culturing the somatic progenitor cells after plating in the presence of T3.

58. The method according to claim 57 wherein said somatic cells induced are glial cells including astrocyte and oligodendrocyte cells.

59. An oligodendrocyte cell prepared by the method according to claim 58 and characterized by RNA transcription of MBP, plp, dm-20 and immunostaining for O4 and NG-2.