초록 ▼

The present invention relates to methods for rapidly expanding a stem cell population with or without culture supplements in simulated microgravity conditions. The present invention relates to methods for rapidly increasing the life span of stem cell populations without culture supplements in simula

The present invention relates to methods for rapidly expanding a stem cell population with or without culture supplements in simulated microgravity conditions. The present invention relates to methods for rapidly increasing the life span of stem cell populations without culture supplements in simulated microgravity conditions. The present invention also relates to methods for increasing the sensitivity of cancer stem cells to chemotherapeutic agents by culturing the cancer stem cells under microgravity conditions and in the presence of omega-3 fatty acids. The methods of the present invention can also be used to proliferate cancer cells by culturing them in the presence of omega-3 fatty acids. The present invention also relates to methods for testing the sensitivity of cancer cells and cancer stem cells to chemotherapeutic agents by culturing the cancer cells and cancer stem cells under microgravity conditions. The methods of the present invention can also be used to produce tissue for use in transplantation by culturing stem cells or cancer stem cells under microgravity conditions. The methods of the present invention can also be used to produce cellular factors and growth factors by culturing stem cells or cancer stem cells under microgravity conditions. The methods of the present invention can also be used to produce cellular factors and growth factors to promote differentiation of cancer stem cells under microgravity conditions.

대표청구항 ▼

1. A method for increasing telomere length in stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB), culturing said stem cells under conditions allowing for telomere growth, isolating said stem cells, and determining the telomere length. 2. The method of claim

1. A method for increasing telomere length in stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB), culturing said stem cells under conditions allowing for telomere growth, isolating said stem cells, and determining the telomere length. 2. The method of claim 1 wherein use of said HFB leads to a low shear environment with a maximum shear force at 10 rpm of about 0.01 dyne/cm2. 3. The method of claim 1 wherein said telomeres are lengthened by about 6-24 repeats as compared to stem cells grown in normal gravity conditions. 4. A method for increasing telomerase activity in stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB), culturing said stem cells under conditions allowing for increased telomerase activity, isolating said stem cells, and determining the telomerase activity. 5. The method of claim 4 wherein use of said HFB leads to a low shear environment with a maximum shear force at 10 rpm of about 0.01 dyne/cm2. 6. A method for increasing the life span of stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB), culturing said stem cells under conditions allowing for increased life span, isolating said stem cells, and determining the telomerase activity in said stem cells, wherein an increase in telomerase length is indicative of increased life span. 7. The method of claim 6 wherein the telomeres of said stem cells are lengthened. 8. The method of claim 6 wherein use of said HFB leads to a low shear environment with a maximum shear force at 10 rpm of about 0.01 dyne/cm2. 9. A method for selectively enriching a stem cell population comprising: seeding a heterogeneous population of cells into a Hydrodynamic Focusing Bioreactor (HFB), the heterogeneous population of cells including one or more stem cells and one or more differentiated cells; andculturing said heterogeneous population of cells under microgravity conditions in the HFB for a period of time sufficient to selectively kill the one or more differentiated cells and selectively enrich the one or more stem cells to thereby selectively enrich the stem cell population. 10. The method of claim 9 wherein the microgravitational force exerted by said HFB is between about 0.01 to about 0.99 g. 11. The method of claim 10 wherein the micro gravitational force exerted by said HFB is about 0.01 g. 12. The method of claim 9 wherein the enriched cell population is CD133+. 13. The method of claim 9 wherein the enriched cell population comprises adult stem cells. 14. The method of claim 9 wherein the enriched cell population comprises cancer stem cells. 15. The method of claim 9 wherein said stem cells are embryonic stem cells. 16. The method of claim 9 wherein said stem cells are grown at a temperature of about 35° C. to about 39° C. 17. The method of claim 16 wherein said stem cells are grown at a temperature of about 37° C. 18. The method of claim 9 wherein said stem cells are cultured in said HFB for about 1 to about 35 days. 19. The method of claim 18 wherein said stem cells are cultured in said HFB for about 7 days. 20. The method of claim 9 wherein said stem cells are cultured at an initial concentration of about 0.0005 to about 1.0×106 cells per ml medium. 21. The method of claim 20 wherein said stem cells are cultured at an initial concentration of about 2.5×105 cells per ml medium. 22. The method of claim 9 wherein the rotational speed of said HFB is from about 1 to about 30 rpm. 23. The method of claim 22 wherein the rotational speed of said HFB is about 25 rpm. 24. The method of claim 9 wherein said stem cells are derived from a cancer patient. 25. The method of claim 24 wherein said cancer patient has a cancer selected from the group consisting of liquid tumor and solid organ tumor. 26. The method of claim 9 wherein said stem cells are derived from a healthy patient. 27. The method of claim 9 wherein said stem cells are genetically modified. 28. The method of claim 9 wherein use of said HFB leads to a low shear environment with a maximum shear force at 10 rpm of about 0.01 dyne/cm2. 29. The method of claim 9 wherein said stem cells are cultured in a culture medium comprising from about 0 to about 20 percent serum, about 1 mM L-Glutamine, 100 U/mL penicillin, and 100 ug/mL Streptomycin. 30. A method for culturing stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB) and culturing said stem cells under conditions allowing for telomere growth. 31. A method for culturing stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB) and culturing said stem cells under conditions allowing for increased telomerase activity. 32. A method for culturing stem cells comprising: seeding said stem cells into a Hydrodynamic Focusing Bioreactor (HFB) and culturing said stem cells under conditions allowing for increased life span. 33. A method for proliferating cancer cells comprising seeding cancer cells into a Hydrodynamic Focusing Bioreactor (HFB) culturing said cancer cells, and allowing said cancer cells to form into cancerous tissue. 34. The method of claim 33 wherein said cancer cells are cultured in the presence of omega-3 fatty acids.