emerging Technology Platforms For Stem Cells the Latest In Applied Stem Cell Research adult And Embryonic Stem Cells Are Set To Play An Integral Part In The New Paradigm Of Personal Medicine And Genetic Therapies. However, Researchers Still Seek To Better Understand These Cells, Their Potential Us
Taking stem cells to the clinic: Major challenges
✍ Scribed by Ariff Bongso; Chui-Yee Fong; Kalamegam Gauthaman
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 259 KB
- Volume
- 105
- Category
- Article
- ISSN
- 0730-2312
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Stem cell therapy offers tremendous promise in the treatment of many incurable diseases. A variety of stem cell types are being studied but human embryonic stem cells (hESCs) appear to be the most versatile as they are pluripotent and can theoretically differentiate into all the tissues of the human body via the three primordial germ layers and the male and female germ lines. Currently, hESCs have been successfully converted in vitro into functional insulin secreting islets, cardiomyocytes, and neuronal cells and transfer of such cells into diabetic, ischaemic, and parkinsonian animal models respectively have shown successful engraftment. However, hESC‐derived tissue application in the human is fraught with the problems of ethics, immunorejection, tumorigenesis from rogue undifferentiated hESCs, and inadequate cell numbers because of long population doubling times in hESCs. Human mesenchymal stem cells (hMSC) though not tumorigenic, also have their limitations of multipotency, immunorejection, and are currently confined to autologous transplantation with the genuine benefits in allogeneic settings not conclusively shown in large controlled human trials. Human Wharton's jelly stem cells (WJSC) from the umbilical cord matrix which are of epiblast origin and containing both hESC and hMSC markers appear to be less troublesome in not being an ethically controversial source, widely multipotent, not tumorigenic, maintain “stemness” for several serial passages and because of short population doubling time can be scaled up in large numbers. This report describes in detail the hurdles all these stem cell types have to overcome before stem cell‐based therapy becomes a genuine reality. J. Cell. Biochem. 105: 1352–1360, 2008. © 2008 Wiley‐Liss, Inc.
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