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Reconstructing blood from induced pluripotent stem cells
The direct reprogramming of human somatic cells to induced pluripotent stem cells (iPSCs) offers exciting prospects for disease modelling and regenerative medicine. Several recent reports support the feasibility of generating various blood cell types from iPSCs through in vitro-directed differentiat...
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Formato: | Texto |
Lenguaje: | English |
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Medicine Reports Ltd
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950048/ https://www.ncbi.nlm.nih.gov/pubmed/20948840 http://dx.doi.org/10.3410/M2-44 |
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author | Papapetrou, Eirini P Sadelain, Michel |
author_facet | Papapetrou, Eirini P Sadelain, Michel |
author_sort | Papapetrou, Eirini P |
collection | PubMed |
description | The direct reprogramming of human somatic cells to induced pluripotent stem cells (iPSCs) offers exciting prospects for disease modelling and regenerative medicine. Several recent reports support the feasibility of generating various blood cell types from iPSCs through in vitro-directed differentiation. However, the derivation of hematopoietic stem cells (HSCs) capable of long-term reconstitution of all hematopoietic lineages appears to be more challenging. These hurdles notwithstanding, cell engineering strategies aiming to correct genetic defects at the stem cell level are already emerging. Robust methodologies for the generation of definitive human HSCs conferring high-level, multilineage, long-term, hematopoietic reconstitution thus are direly needed before the therapeutic potential and safety of iPSC-derived cell products can be thoroughly investigated. |
format | Text |
id | pubmed-2950048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Medicine Reports Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-29500482010-10-14 Reconstructing blood from induced pluripotent stem cells Papapetrou, Eirini P Sadelain, Michel F1000 Med Rep Review Article The direct reprogramming of human somatic cells to induced pluripotent stem cells (iPSCs) offers exciting prospects for disease modelling and regenerative medicine. Several recent reports support the feasibility of generating various blood cell types from iPSCs through in vitro-directed differentiation. However, the derivation of hematopoietic stem cells (HSCs) capable of long-term reconstitution of all hematopoietic lineages appears to be more challenging. These hurdles notwithstanding, cell engineering strategies aiming to correct genetic defects at the stem cell level are already emerging. Robust methodologies for the generation of definitive human HSCs conferring high-level, multilineage, long-term, hematopoietic reconstitution thus are direly needed before the therapeutic potential and safety of iPSC-derived cell products can be thoroughly investigated. Medicine Reports Ltd 2010-06-16 /pmc/articles/PMC2950048/ /pubmed/20948840 http://dx.doi.org/10.3410/M2-44 Text en © 2010 Medicine Reports Ltd http://creativecommons.org/licenses/by-nc/3.0/legalcode This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. You may not use this work for commercial purposes |
spellingShingle | Review Article Papapetrou, Eirini P Sadelain, Michel Reconstructing blood from induced pluripotent stem cells |
title | Reconstructing blood from induced pluripotent stem cells |
title_full | Reconstructing blood from induced pluripotent stem cells |
title_fullStr | Reconstructing blood from induced pluripotent stem cells |
title_full_unstemmed | Reconstructing blood from induced pluripotent stem cells |
title_short | Reconstructing blood from induced pluripotent stem cells |
title_sort | reconstructing blood from induced pluripotent stem cells |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2950048/ https://www.ncbi.nlm.nih.gov/pubmed/20948840 http://dx.doi.org/10.3410/M2-44 |
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