The SAGE Encyclopedia of Stem Cell Research. Группа авторов

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The SAGE Encyclopedia of Stem Cell Research - Группа авторов

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primary immunodeficiency diseases such as AIDS, adult stem cells offer the promise of treating such conditions through stem cell therapy. Pluripotent stem cells, the master cells capable of generating cells from the three basic body layers, such as adult stem cells, can self-renew. In so doing, they are able to regenerate the missing immune cells at the basis of nearly all primary immunodeficiency illnesses. The transplantation of reconstituted stem cells using normal genes could therefore restore the immune function and provide a new quality of life to affected individuals.

      What are the challenges to the use of adult stem cells?

      For many years, adult stem cells have been used therapeutically in the form of bone marrow transplants. Nevertheless, the scientific community is still facing today a series of challenges that need to be overcome before stem cells can be deemed ready to effectively treat a wider range of diseases.

      Researchers are still attempting to grasp the unique molecular and genetic basis for the phenomenon enabling these cells to replicate endlessly. As we can see, challenges pertaining to the immune system constitute a significant impediment to the reliable application of stem cell therapies.

      Cell therapy surely provides exceptional prospects to disease treatment, yet the value of these technological accomplishments will only be fully realized once the therapeutic techniques underway are carefully applied to patients through clinical programs capable of ensuring efficacious and tangible results at a reasonable cost.

      Morenike Trenou

      Independent Scholar

      See Also: Embryonic Stem Cells, Methods to Produce; Pluripotent Stem Cells, Embryonic; Pluripotent Stem Cells, Germ; Stem Cell Markers.

      Further Readings

      Abraham, E. J., C. A. Leech, J. C. Lin, et al. “Insulinotropic Hormone Glucagon-Like Peptide-1 Differentiation of Human Pancreatic Islet-Derived Progenitor Cells Into Insulin-Producing Cells.” Endocrinology, v.143 (2002).

      Alison, M. R., R. Poulsom, R. Jeffery, et al. “Hepatocytes From Non-Hepatic Adult Stem Cells.” Nature, v.406/6793 (2002).

      American Diabetes Association. “Economic Costs of Diabetes in the U.S. in 2007.” Diabetes Care, v.31 (2008).

      Audet, J., C. L. Miller, S. Rose-John, et al. “Distinct Role of gp130 Activation in Promoting Self-Renewal Divisions by Mitogenically Stimulated Murine Hematopoietic Stem Cells.” Proceedings of the National Academy of Sciences of the USA, v.98/4 (February 13, 2001).

      Baeyens, L., S. De Breuck, J. Lardon, et al. “In Vitro Generation of Insulin-Producing Beta Cells From Adult Exocrine Pancreatic Cells.” Diabetologia, v.48 (2005).

      Baum, C. M., I. L.Weissman, A. S. Tsukamoto, et al. “Isolation of a Candidate Human Hematopoietic Stem-Cell Population.” Proceedings of the National Academy of Sciences of the USA, v.89 (1992).

      Bittner, R. E., C. Schöfer, K. Weipoltshammer, et al. “Recruitment of Bone-Marrow-Derived Cells by Skeletal and Cardiac Muscle in Adult Dystrophic mdx Mice.” Anatomy and Embryology (Berl), v.199/5 (1999).

      Boiani, M., S. Eckardt, H. R. Schöler, et al. “Oct4 Distribution and Level in Mouse Clones: Consequences for Pluripotency.” Genes and Development, v.16/10 (2002).

      Centers for Disease Control and Prevention. “National Diabetes Fact Sheet: General Information and National Estimates on Diabetes in the United States, 2005.” http://www.cdc.gov/diabetes/pubs/pdf/ndfs_2005.pdf (Accessed April 24, 2008).

      Chen, J., C. M. Astle, and D. E. Harrison. “Development and Aging of Primitive Hematopoietic Stem Cells in BALB/cBy Mice.” Experimental Hematology, v./5 (1999).

      Childs, R., A. Chernoff, N. Contentin, et al. “Regression of Metastatic Renal-Cell Carcinoma after Nonmyeloablative Allogeneic Peripheral-Blood Stem-Cell Transplantation. New England Journal of Medicine, v.343 (2000).

      Cutler, C. and J. H. Antin. “Peripheral Blood Stem Cells for Allogeneic Transplantation: A Review.” Stem Cells, v.19 (2001).

      De Filippo, R. E., J. J. Yoo, and A. Atala. “Engineering of Vaginal Tissue in Vivo.” Tissue Engineering, v.9 (2003).

      de Miguel, M. P., S. Fuentes-Julián, and Y. Alcaina, “Pluripotent Stem Cells: Origin, Maintenance and Induction.” Stem Cell Reviews and Reports, v.6/4 (2010).

      Doetschman, T., H. Eistetter, M. Katz, et al. “The in Vitro Development of Blastocyst-Derived Embryonic Stem Cell Lines: Formation of Visceral Yolk Sac, Blood Islands and Myocardium.” Journal of Embryology and Experimental Morphology, v.87 (1985).

      Domen, J. and I. L. Weissman. “Hematopoietic Stem Cells Need Two Signals to Prevent Apoptosis; BCL-2 Can Provide One of These, Kitl/c-Kit Signaling the Other.” Journal of Experimental Medicine, v.192/12 (2000).

      Dor, Y., J. Brown, O. I. Martinez, et al. “Adult Pancreatic Beta-Cells Are Formed by Self-duplication Rather Than Stem-Cell Differentiation.” Nature, v.429 (2004).

      Dzierzak, E. “Embryonic Beginnings of Definitive Hematopoietic Stem Cells.” Annals of the New York Academy of Sciences, v.872 (1999).

      Dzierzak, E., A. Medvinsky, and M. de Bruijn. “Qualitative and Quantitative Aspects of Hematopoietic Cell Development in the Mammalian Embryo.” Immunology Today, v.19/5 (1998).

      Ema, H., H. Takano, K. Sudo, et al. “In Vitro Self-Renewal Division of Hematopoietic Stem Cells.” Journal of Experimental Medicine, v.192/9 (2000).

      Evans, M. J. and M. H. Kaufman. “Establishment in Culture of Pluripotential Cells From Mouse Embryos.” Nature, v.292/5819 (1981).

      Ferranninni, E. “Insulin Resistance Versus Insulin Deficiency in Non-Insulin-Dependent Diabetes Mellitus: Problems and Prospects.” Endocrine Reviews, v.19. (1998).

      Gallacher, L., B. Murdoch, D. Wu, et al. “Identification of Novel Circulating Human Embryonic Blood Stem Cells.” Blood, v.96/5 (2000).

      Guz, Y., I. Nasir, and G. Teitelman. “Regeneration of Pancreatic Beta Cells From Intra-Islet Precursor Cells in an Experimental Model of Diabetes.” Endocrinology, v.142 (2001).

      Hill, J. O. and J. C. Peters. “Environmental Contributions to the Obesity Epidemic.” Science, v.280 (1998).

      Hull, M. G., C. M. Glazener, N. J. Kelly, et al. “Population Study of Causes, Treatment, and Outcome of Infertility.” British Medical Journal, v.291/6510 (1985).

      King, H., R. E. Aubert, and W. H. Herman. “Global Burden of Diabetes, 1995–2025: Prevalence, Numerical Estimates, and Projections.” Diabetes Care, v.21 (1998).

      Kolios, G. and Y. Moodley. “Introduction to Stem Cells and Regenerative Medicine.” Respiration, v.85/1 (2013).

      Lee, C. S., D. D. De Leon, K. H. Kaestner, et al. “Regeneration of Pancreatic Islets After Partial Pancreatectomy in Mice Does Not Involve the Reactivation of Neurogenin-3.” Diabetes, v.55 (2006).

      Lipsett,

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