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Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming
Possessing the ability of self-renewal with immortalization and potential for differentiation into different cell types, stem cells, particularly embryonic stem cells (ESC), have attracted significant attention since their discovery. As ESC research has played an essential role in developing our und...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736417/ https://www.ncbi.nlm.nih.gov/pubmed/26880993 http://dx.doi.org/10.1155/2016/8415010 |
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author | Ji, Pengfei Manupipatpong, Sasicha Xie, Nina Li, Yujing |
author_facet | Ji, Pengfei Manupipatpong, Sasicha Xie, Nina Li, Yujing |
author_sort | Ji, Pengfei |
collection | PubMed |
description | Possessing the ability of self-renewal with immortalization and potential for differentiation into different cell types, stem cells, particularly embryonic stem cells (ESC), have attracted significant attention since their discovery. As ESC research has played an essential role in developing our understanding of the mechanisms underlying reproduction, development, and cell (de)differentiation, significant efforts have been made in the biomedical study of ESC in recent decades. However, such studies of ESC have been hampered by the ethical issues and technological challenges surrounding them, therefore dramatically inhibiting the potential applications of ESC in basic biomedical studies and clinical medicine. Induced pluripotent stem cells (iPSCs), generated from the reprogrammed somatic cells, share similar characteristics including but not limited to the morphology and growth of ESC, self-renewal, and potential differentiation into various cell types. The discovery of the iPSC, unhindered by the aforementioned limitations of ESC, introduces a viable alternative to ESC. More importantly, the applications of iPSC in the development of disease models such as neurodegenerative disorders greatly enhance our understanding of the pathogenesis of such diseases and also facilitate the development of clinical therapeutic strategies using iPSC generated from patient somatic cells to avoid an immune rejection. In this review, we highlight the advances in iPSCs generation methods as well as the mechanisms behind their reprogramming. We also discuss future perspectives for the development of iPSC generation methods with higher efficiency and safety. |
format | Online Article Text |
id | pubmed-4736417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47364172016-02-15 Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming Ji, Pengfei Manupipatpong, Sasicha Xie, Nina Li, Yujing Stem Cells Int Review Article Possessing the ability of self-renewal with immortalization and potential for differentiation into different cell types, stem cells, particularly embryonic stem cells (ESC), have attracted significant attention since their discovery. As ESC research has played an essential role in developing our understanding of the mechanisms underlying reproduction, development, and cell (de)differentiation, significant efforts have been made in the biomedical study of ESC in recent decades. However, such studies of ESC have been hampered by the ethical issues and technological challenges surrounding them, therefore dramatically inhibiting the potential applications of ESC in basic biomedical studies and clinical medicine. Induced pluripotent stem cells (iPSCs), generated from the reprogrammed somatic cells, share similar characteristics including but not limited to the morphology and growth of ESC, self-renewal, and potential differentiation into various cell types. The discovery of the iPSC, unhindered by the aforementioned limitations of ESC, introduces a viable alternative to ESC. More importantly, the applications of iPSC in the development of disease models such as neurodegenerative disorders greatly enhance our understanding of the pathogenesis of such diseases and also facilitate the development of clinical therapeutic strategies using iPSC generated from patient somatic cells to avoid an immune rejection. In this review, we highlight the advances in iPSCs generation methods as well as the mechanisms behind their reprogramming. We also discuss future perspectives for the development of iPSC generation methods with higher efficiency and safety. Hindawi Publishing Corporation 2016 2016-01-05 /pmc/articles/PMC4736417/ /pubmed/26880993 http://dx.doi.org/10.1155/2016/8415010 Text en Copyright © 2016 Pengfei Ji et al. https://creativecommons.org/licenses/by/4.0/ 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 Ji, Pengfei Manupipatpong, Sasicha Xie, Nina Li, Yujing Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming |
title | Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming |
title_full | Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming |
title_fullStr | Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming |
title_full_unstemmed | Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming |
title_short | Induced Pluripotent Stem Cells: Generation Strategy and Epigenetic Mystery behind Reprogramming |
title_sort | induced pluripotent stem cells: generation strategy and epigenetic mystery behind reprogramming |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736417/ https://www.ncbi.nlm.nih.gov/pubmed/26880993 http://dx.doi.org/10.1155/2016/8415010 |
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