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Year 2015, Volume: 36 Issue: 3, 2009 - 2015, 13.05.2015

Abstract

References

  • Jiang Y, Henderson D, Blackstad M et al. Neuroectodermal differentiation from mouse multipotent adult progenitor cells. Proc Natl Acad Sci U S A 2003;100 (Suppl 1):11854– 11860.
  • Reyes M, Lund T, Lenvik T et al. Purification and ex vivo expansion of postnatal human marrow mesodermal progenitor cells. Blood 2001;98:2615–2625.
  • Schwartz RE, Reyes M, Koodie L et al. Multipotent adult progenitor cells from bone marrow differentiate into functional hepatocyte-like cells. J Clin Invest 2002;109:1291– 1302.
  • Scheffler B,Walton N.M.,2005.Phenotypic and functional characterization of adult brain neuropoiesis. Proc. Natl. Acad. Sci. USA 102,9353 -9358.

The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep

Year 2015, Volume: 36 Issue: 3, 2009 - 2015, 13.05.2015

Abstract

The main problem with embryonic stem cell research is the tissue incompatibility. Millions of lines must be established in order to serve a significant percentage of potential patients. The use of autologous adult stem cells (cells from the patient) eliminates the problems with tumorogenesis, mutation, and tissue incompatibility.Multipotent stem cells can be found in the numerous adult tissues. The isolation and expansion of neural cell types has become increasinglyrelevant in restorative neurobiology. To examine the developmentalpotential of adult  sheep brain cells, we applied conditionsfavoring the growth of neural stem cells and bone marrow stem cells  to multiple corticalregions, resulting in the identification and selection of apopulation of adult sheep neural progenitors.. It has also been seen that BMSC can differentiate into neural cells and therefore can be used for restoration of brain damage. We tested the theory that BMSC could change into neural precursor cells by co culturing BMSC, identified by using β-galatosidase, with fetal primary neuronal cultures. We concluded that, our findings suggestan unprecedented developmental plasticity and proliferative  potential are retained in CNS glia throughout life and the use of autologous adult stem cells  eliminates the problems with tumor genesis, mutation, and tissue incompatibility in both NSC,s and ESC,s therapy.

References

  • Jiang Y, Henderson D, Blackstad M et al. Neuroectodermal differentiation from mouse multipotent adult progenitor cells. Proc Natl Acad Sci U S A 2003;100 (Suppl 1):11854– 11860.
  • Reyes M, Lund T, Lenvik T et al. Purification and ex vivo expansion of postnatal human marrow mesodermal progenitor cells. Blood 2001;98:2615–2625.
  • Schwartz RE, Reyes M, Koodie L et al. Multipotent adult progenitor cells from bone marrow differentiate into functional hepatocyte-like cells. J Clin Invest 2002;109:1291– 1302.
  • Scheffler B,Walton N.M.,2005.Phenotypic and functional characterization of adult brain neuropoiesis. Proc. Natl. Acad. Sci. USA 102,9353 -9358.
There are 4 citations in total.

Details

Primary Language English
Subjects Engineering
Journal Section Special
Authors

M.e Akbarı

Sh Salehın This is me

Publication Date May 13, 2015
Published in Issue Year 2015 Volume: 36 Issue: 3

Cite

APA Akbarı, M., & Salehın, S. (2015). The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi, 36(3), 2009-2015.
AMA Akbarı M, Salehın S. The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi. May 2015;36(3):2009-2015.
Chicago Akbarı, M.e, and Sh Salehın. “The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep”. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi 36, no. 3 (May 2015): 2009-15.
EndNote Akbarı M, Salehın S (May 1, 2015) The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi 36 3 2009–2015.
IEEE M. Akbarı and S. Salehın, “The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep”, Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi, vol. 36, no. 3, pp. 2009–2015, 2015.
ISNAD Akbarı, M.e - Salehın, Sh. “The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep”. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi 36/3 (May 2015), 2009-2015.
JAMA Akbarı M, Salehın S. The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi. 2015;36:2009–2015.
MLA Akbarı, M.e and Sh Salehın. “The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep”. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi, vol. 36, no. 3, 2015, pp. 2009-15.
Vancouver Akbarı M, Salehın S. The Study of Comparative Nsc, S And Bmsc, S Neurons Therapy For Treatment of Artificially Created Neuron Disorders In Sheep. Cumhuriyet Üniversitesi Fen Edebiyat Fakültesi Fen Bilimleri Dergisi. 2015;36(3):2009-15.