Culture System and Method for Propagation of Human Blastocyst-Derived Stem Cells

• US 20090269830A1
• Filed: 03/16/2007
• Published: 10/29/2009
• Est. Priority Date: 03/17/2006
• Status: Abandoned Application

• Current Assignee: Cellartis AB (Ningbo Junsheng Investment Group Co., Ltd.)
• Original Assignee: Cellartis AB (Ningbo Junsheng Investment Group Co., Ltd.)
• Inventors: Ellerstrom, Catharina, Semb, Henrik, Strehl, Raimund
• Application Number:
  US12/225,201
• Publication Number:
  US 20090269830A1
• Time in Patent Office: Days
• US Class Current: 435/213
• CPC Class Codes: C12N 2501/115 Basic fibroblast growth factor (bFGF, FGF-2)
• CPC Class Codes: C12N 2502/13 connective tissue cells; generic mesenchyme cells, e.g. so-called "embryonic fibroblasts"
• CPC Class Codes: C12N 2502/1323 Adult fibroblasts
• CPC Class Codes: C12N 2502/99 genetically modified cells
• CPC Class Codes: C12N 2509/00 Methods for the dissociation of cells, e.g. specific use of enzymes
• 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

Abstract

The present invention relates to a culture system for and a method for propagation of human blastocyst-derived stem cells (hBS cells) upon enzymatic dissociation into a single cell suspension. The culture system for propagation of human blastocyst-derived stem (hBS) cells comprises

• i) human feeder cells at a density of at least 50,000 cells/cm²,
• ii) one or more dissociation agents for dissociation of hBS cell colonies into a single cell suspension, and
• iii) a supportive culture medium,
  which culture system makes it possible to propagate hBS cells by dissociation of hBS cell colonies into a single cell suspension at each consecutive passage for an extended time period, while maintaining the significant characteristics of hBS cells.

Claims

1. A culture system for propagation of human blastocyst-derived stem (hBS) cells comprising

i) human feeder cells at a density of at least 50,000 cells/cm²,

ii) one or more dissociation agents for dissociation of hBS cell colonies into a single cell suspension, and

iii) a supportive culture medium.

2. A culture system according to claim 1, wherein the density of human feeder cells is from about 50,000 to about 500,000 cells/cm².

3. A culture system according to claim 1, wherein the human feeder cells are derived from human tissue.

4. A culture system according to claim 3, wherein the human tissue is derived from embryonic, fetal, neonatal, juvenile, or adult tissue.

5. A culture system according to claim 3, wherein the human tissue is derived from skin, including foreskin, umbilical chord, muscle, lung, epithelium, placenta, fallopian tube, glandula, stroma or breast.

6. A culture system according to claim 1, wherein the human feeder cells are derived in vitro from hBS cells or cells derived from hBS cells.

7. A culture system according to claim 1, wherein the human feeder cells are derived from cell types pertaining to the group consisting of human fibroblasts, fibrocytes, myocytes, keratinocytes, endothelial cells and epithelial cells.

8. A culture system according to claim 1, wherein the human feeder cells are fibroblasts.

9. A culture system according to claim 8, wherein the feeder cells are derived from human neonatal foreskin fibroblasts.

10. A culture system according to claim 6, wherein the cells derived from hBS cells are fibroblasts or have a mesenchymal phenotype.

11. A culture system according to claim 1, wherein the human feeder cells are derived from embryonic fibroblasts, extraembryonic endoderm cells, extraembryonic mesoderm cells, fetal fibroblasts and/or fibrocytes, fetal muscle cells, fetal skin cells, fetal lung cells, fetal endothelial cells, fetal epithelial cells, umbilical chord mesenchymal cells, placental fibroblasts and/or fibrocytes, placental endothelial cells, post-natal human foreskin fibroblasts and/or fibrocytes, post-natal muscle cells, post-natal skin cells, post-natal endothelial cells, adult skin fibroblasts and/or fibrocytes, adult muscle cells, adult fallopian tube endothelial cells, adult glandular endometrial cells, adult stromal endometrial cells, adult breast cancer parenchymal cells, adult endothelial cells, adult epithelial cells or adult keratinocytes.

12. A culture system according to claim 1, wherein the human feeder cells have been growth inactivated.

13. A culture system according to claim 12, wherein the human feeder cells have been growth inactivated by mitomycin treatment.

14. A culture system according to claim 12, wherein the human feeder cells have been growth inactivated by irradiation.

15. A culture system according to claim 1, wherein the human feeder cells are seeded from about 1 to about 10 days prior to seeding the hBS cells.

16. A culture system according to claim 15, wherein the culture medium is changed at least one time prior to seeding the hBS cells.

17. A culture system according to claim 1, wherein one or more dissociation agents is an enzyme.

18. A culture system according to claim 17, wherein the enzyme is a proteolytic enzyme.

19. A culture system according to claim 17, wherein the enzyme is a collagenolytic enzyme.

20. A culture system according to claim 17, wherein the enzyme is selected from the group consisting of trypsin, trypsin-like, dispase, dispase-like, pronase, pronase-like, collagenase, collagense-like and matrix metalloproteinases.

21. A culture system according to claim 17, wherein the enzyme is a recombinant enzyme.

22. A culture system according to claim 1, wherein one or more dissociation agents is a chelating agent.

23. A culture system according to claim 22, wherein the chelating agent is a chelator of divalent cations.

24. A culture system according to claim 22, wherein the chelating agent is selected from the group consisting of EDTA, EGTA and HEDTA.

25. A culture system according to claim 1, wherein the one or more dissociation agents is a combination of at least two dissociation agents.

26. A culture system according to claim 25, wherein the combination of dissociation agents comprises one or more enzymes and one or more chelating agents.

27. A culture system according to claim 25, wherein the combination of dissociation agents is xeno-free.

28. A culture system according to claim 25, wherein the combination of dissociation agents is selected from the group of commercially available combinations consisting of TrypLE™

Select, Accutase™ and

Accumax™

.

29. A culture system according to claim 1, wherein the supportive culture medium is selected from the group consisting of DMEM and IMDM.

30. A culture system according to claim 1, wherein the supportive culture medium is supplemented with from about 0.5 to about 1000 ng/ml hrbFGF.

31. A culture system according to claim 1, wherein the supportive culture medium is supplemented with from about 1 to about 40% serum.

32. A culture system according to claim 31, wherein the serum is FBS or human serum.

33. A culture system according to claim 1, the culture system comprising

i) human neonatal foreskin feeder cells at a density of at least 70,000 cells/cm²,

ii) TrypLE™

Select for dissociation of hBS cell colonies into a single cell suspension, and

iii) VitroHES™

supplemented with at least 4 ng/ml hrbFGF supportive culture medium, which culture system makes it possible to propagate hBS cells by dissociation of hBS cell colonies into a single cell suspension at each consecutive passage for an extended time period, while maintaining the significant characteristics of hBS cells.

34. A method for propagation of hBS cells in a culture system as defined in claim 1, the method comprising the steps of:

i) optionally, performing an adjustment procedure in order for the hBS cells obtained from a master cell line to adjust to the culture system,

ii) dissociating the hBS cells into a single cell suspension by the use of one or more dissociation agents,

iii) distributing the single cell suspension in a split ratio of at least 1;

4 into one or more culture vessels comprising human feeder cells at a density of at least 50,000 cells/cm², iv) incubating the hBS cells for from about 3 to about 25 days upon regular medium changes, and

v) repeating n times from step ii), wherein n is an integer of at least 1,

in order to propagate the hBS cells, while maintaining the significant characteristics of such cells.

35. A method according to claim 34, further comprising the steps of:

vi) analyzing the cells obtained in step iv) to see whether the significant characteristics of hBS cells are maintained, and

vii) repeating from step ii) if the significant characteristics of hBS cells are maintained.

36. A method according to claim 34, wherein n is at least 5.

37. A method according to claim 34, wherein the dissociation of hBS cell colonies into a single cell suspension in step ii) is performed by treating the hBS cell colonies with one or more dissociation agents.

38. A method according to claim 34, wherein the effect of the one or more dissociation agents is diminished prior to step iii).

39. A method according to claim 38, wherein the effect of the one or more dissociation agents is diminished by physical removal of the one or more dissociation agents, dilution of the one or more dissociation agents, addition of one or more inhibitors of the one or more dissociation agents, addition of one or more substrates of the one or more dissociation agents in excess or inherent auto-inhibition of the one or more dissociation agents.

40. A method according to claim 34, wherein the split ratio is from about 1:

4 to about 1;

5000.

41. A method according to claim 40, wherein the split ratio is 1:

20.

42. A method according to claim 34, wherein the hBS cells obtained in step iii) are incubated for from about 3 to about 25 days.

43. A method according to claim 34, wherein the medium changes in step iv) are performed from about 1 to about 14 times a week.

44. A method according to claim 34, wherein the adjustment procedure comprises the steps of:

a) dissociating the hBS cell colonies into a single cell suspension by use of one or more dissociation agents,

b) distributing the single cell suspension in a split ratio of at least 1;

3 into one or more culture vessels comprising human feeder cells at a density of at least 50,000 cells/cm²,

c) incubating the hBS cells for from about 5 to about 30 days upon medium changes at regular time intervals, and

d) optionally, repeating from step a) at the most 5 times,

in order to obtain homogeneous undifferentiated hBS cells colonies.

45. A method according to claim 44, wherein the hBS cells obtained in step c) are incubated for from about 5 to about 30 days.

46. A method according to claim 44, wherein step d) is included.

47. A method according to claim 46, wherein repetition from step a) is performed at the most 5 times.

48. A method according to claim 44, wherein the medium changes in step c) are performed from about 1 to about 14 times a week.

49. A method according to claim 34, comprising the steps of

i) performing an adjustment procedure comprising the steps of a) dissociating the hBS cell colonies into a single cell suspension by use of one or more dissociation agents, b) distributing the single cell suspension in a split ratio of at least 1:

3 into one or more culture vessels comprising human feeder cells at a density of at least 50,000 cells/cm², c) incubating the hBS cells for from about 5 to about 30 days upon medium changes at regular time intervals, d) repeating from step a) at the most 5 times, in order to obtain homogeneous undifferentiated hBS cells colonies,

ii) dissociating the hBS cells into a single cell suspension by the use one or more dissociation agents,

iii) distributing the single cell suspension in a split ratio of at least 1;

4 into one or more culture vessels comprising human feeder cells at a density of at least 50,000 cells/cm²,

iv) incubating the hBS cells for from about 3 to about 25 days upon regular medium changes, and

v) repeating at least 20 times from step ii),

in order to propagate the hBS cells, while maintaining the significant characteristics of such cells.

50. A single cell suspension of hBS cells, wherein less than 10% of the cells appear as clusters of cells, the single cell suspension being capable of surviving and maintaining the significant characteristics of hBS cells for more than 20 passages, when subjected to a method for propagation of such cells as defined in claim 34.

51. A xeno-free single cell suspension of hBS cells, wherein less than 10% of the cells appear as clusters of cells, the single cell suspension being capable of surviving and maintaining the significant characteristics of hBS cells for more than 20 passages, when subjected to a method for propagation of such cells as defined in claim 34.

52. An improved cell line from hBS cells, which is capable of surviving and maintaining the significant characteristics of hBS cells for more than 20 passages, when subjected to a method for propagation of such cells as defined in claim 34.

58. A kit comprising the following components:

i) a single hBS cell population obtainable by a method as defined in claim 34, and

ii) a user manual describing a method for propagation of the hBS cells.

60. A kit comprising, a first component comprising i) a single cell population obtainable by a method as defined in claim 34,

and at least one of the following components

ii) human feeder cells,

iii) one or more dissociation agents for dissociation of hBS cell colonies into a single cell suspension, and

iv) a supportive culture medium.

61. A kit according to claim 58, wherein the single cell population is derived from a xeno-free derived hBS cell line and any other components are xeno-free.

53-57. -57. (canceled)

59. (canceled)