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Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature
The complexity of human pluripotent stem cell (hPSC) fate represents both opportunity and challenge. In theory, all somatic cell types can be differentiated from hPSCs, opening the door to many opportunities in transplant medicine. However, such clinical applications require high standards of purity...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972883/ https://www.ncbi.nlm.nih.gov/pubmed/27547711 http://dx.doi.org/10.1007/s40778-016-0060-6 |
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author | West, Michael D. Nasonkin, Igor Larocca, David Chapman, Karen B. Binette, Francois Sternberg, Hal |
author_facet | West, Michael D. Nasonkin, Igor Larocca, David Chapman, Karen B. Binette, Francois Sternberg, Hal |
author_sort | West, Michael D. |
collection | PubMed |
description | The complexity of human pluripotent stem cell (hPSC) fate represents both opportunity and challenge. In theory, all somatic cell types can be differentiated from hPSCs, opening the door to many opportunities in transplant medicine. However, such clinical applications require high standards of purity and identity, that challenge many existing protocols. This underscores the need for increasing precision in the description of cell identity during hPSC differentiation. We highlight one salient example, namely, the numerous published reports of hPSC-derived mesenchymal stem cells (MSCs). We suggest that many of these reports likely represent an improper use of certain cluster of differentiation (CD) antigens in defining bone marrow-derived MSCs. Instead, most such hPSC-derived mesenchymal cells are likely a complex mixture of embryonic anlagen, primarily of diverse mesodermal and neural crest origins, making precise identification, reproducible manufacture, and uniform differentiation difficult to achieve. We describe a potential path forward that may provide more precision in nomenclature, and cells with higher purity and identity for potential therapeutic use. |
format | Online Article Text |
id | pubmed-4972883 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-49728832016-08-17 Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature West, Michael D. Nasonkin, Igor Larocca, David Chapman, Karen B. Binette, Francois Sternberg, Hal Curr Stem Cell Rep Stem Cells: Policies from the Bench to the Clinic (AI Caplan and TL Bonfield, Section Editors) The complexity of human pluripotent stem cell (hPSC) fate represents both opportunity and challenge. In theory, all somatic cell types can be differentiated from hPSCs, opening the door to many opportunities in transplant medicine. However, such clinical applications require high standards of purity and identity, that challenge many existing protocols. This underscores the need for increasing precision in the description of cell identity during hPSC differentiation. We highlight one salient example, namely, the numerous published reports of hPSC-derived mesenchymal stem cells (MSCs). We suggest that many of these reports likely represent an improper use of certain cluster of differentiation (CD) antigens in defining bone marrow-derived MSCs. Instead, most such hPSC-derived mesenchymal cells are likely a complex mixture of embryonic anlagen, primarily of diverse mesodermal and neural crest origins, making precise identification, reproducible manufacture, and uniform differentiation difficult to achieve. We describe a potential path forward that may provide more precision in nomenclature, and cells with higher purity and identity for potential therapeutic use. Springer International Publishing 2016-07-28 2016 /pmc/articles/PMC4972883/ /pubmed/27547711 http://dx.doi.org/10.1007/s40778-016-0060-6 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Stem Cells: Policies from the Bench to the Clinic (AI Caplan and TL Bonfield, Section Editors) West, Michael D. Nasonkin, Igor Larocca, David Chapman, Karen B. Binette, Francois Sternberg, Hal Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature |
title | Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature |
title_full | Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature |
title_fullStr | Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature |
title_full_unstemmed | Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature |
title_short | Adult Versus Pluripotent Stem Cell-Derived Mesenchymal Stem Cells: The Need for More Precise Nomenclature |
title_sort | adult versus pluripotent stem cell-derived mesenchymal stem cells: the need for more precise nomenclature |
topic | Stem Cells: Policies from the Bench to the Clinic (AI Caplan and TL Bonfield, Section Editors) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972883/ https://www.ncbi.nlm.nih.gov/pubmed/27547711 http://dx.doi.org/10.1007/s40778-016-0060-6 |
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