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Technical Challenges in the Derivation of Human Pluripotent Cells

It has long been discovered that human pluripotent cells could be isolated from the blastocyst state of embryos and called human embryonic stem cells (ESCs). These cells can be adapted and propagated indefinitely in culture in an undifferentiated manner as well as differentiated into cell representi...

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Detalles Bibliográficos
Autores principales: Noisa, Parinya, Parnpai, Rangsun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138062/
https://www.ncbi.nlm.nih.gov/pubmed/21776284
http://dx.doi.org/10.4061/2011/907961
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author Noisa, Parinya
Parnpai, Rangsun
author_facet Noisa, Parinya
Parnpai, Rangsun
author_sort Noisa, Parinya
collection PubMed
description It has long been discovered that human pluripotent cells could be isolated from the blastocyst state of embryos and called human embryonic stem cells (ESCs). These cells can be adapted and propagated indefinitely in culture in an undifferentiated manner as well as differentiated into cell representing the three major germ layers: endoderm, mesoderm, and ectoderm. However, the derivation of human pluripotent cells from donated embryos is limited and restricted by ethical concerns. Therefore, various approaches have been explored and proved their success. Human pluripotent cells can also be derived experimentally by the nuclear reprogramming of somatic cells. These techniques include somatic cell nuclear transfer (SCNT), cell fusion and overexpression of pluripotent genes. In this paper, we discuss the technical challenges of these approaches for nuclear reprogramming, involving their advantages and limitations. We will also highlight the possible applications of these techniques in the study of stem cell biology.
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spelling pubmed-31380622011-07-20 Technical Challenges in the Derivation of Human Pluripotent Cells Noisa, Parinya Parnpai, Rangsun Stem Cells Int Review Article It has long been discovered that human pluripotent cells could be isolated from the blastocyst state of embryos and called human embryonic stem cells (ESCs). These cells can be adapted and propagated indefinitely in culture in an undifferentiated manner as well as differentiated into cell representing the three major germ layers: endoderm, mesoderm, and ectoderm. However, the derivation of human pluripotent cells from donated embryos is limited and restricted by ethical concerns. Therefore, various approaches have been explored and proved their success. Human pluripotent cells can also be derived experimentally by the nuclear reprogramming of somatic cells. These techniques include somatic cell nuclear transfer (SCNT), cell fusion and overexpression of pluripotent genes. In this paper, we discuss the technical challenges of these approaches for nuclear reprogramming, involving their advantages and limitations. We will also highlight the possible applications of these techniques in the study of stem cell biology. SAGE-Hindawi Access to Research 2011-06-19 /pmc/articles/PMC3138062/ /pubmed/21776284 http://dx.doi.org/10.4061/2011/907961 Text en Copyright © 2011 P. Noisa and R. Parnpai. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Noisa, Parinya
Parnpai, Rangsun
Technical Challenges in the Derivation of Human Pluripotent Cells
title Technical Challenges in the Derivation of Human Pluripotent Cells
title_full Technical Challenges in the Derivation of Human Pluripotent Cells
title_fullStr Technical Challenges in the Derivation of Human Pluripotent Cells
title_full_unstemmed Technical Challenges in the Derivation of Human Pluripotent Cells
title_short Technical Challenges in the Derivation of Human Pluripotent Cells
title_sort technical challenges in the derivation of human pluripotent cells
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3138062/
https://www.ncbi.nlm.nih.gov/pubmed/21776284
http://dx.doi.org/10.4061/2011/907961
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