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Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells
Joint injury and osteoarthritis affect millions of people worldwide, but attempts to generate articular cartilage using adult stem/progenitor cells have been unsuccessful. We hypothesized that recapitulation of the human developmental chondrogenic program using pluripotent stem cells (PSCs) may repr...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871393/ https://www.ncbi.nlm.nih.gov/pubmed/24371811 http://dx.doi.org/10.1016/j.stemcr.2013.10.012 |
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author | Wu, Ling Bluguermann, Carolina Kyupelyan, Levon Latour, Brooke Gonzalez, Stephanie Shah, Saumya Galic, Zoran Ge, Sundi Zhu, Yuhua Petrigliano, Frank A. Nsair, Ali Miriuka, Santiago G. Li, Xinmin Lyons, Karen M. Crooks, Gay M. McAllister, David R. Van Handel, Ben Adams, John S. Evseenko, Denis |
author_facet | Wu, Ling Bluguermann, Carolina Kyupelyan, Levon Latour, Brooke Gonzalez, Stephanie Shah, Saumya Galic, Zoran Ge, Sundi Zhu, Yuhua Petrigliano, Frank A. Nsair, Ali Miriuka, Santiago G. Li, Xinmin Lyons, Karen M. Crooks, Gay M. McAllister, David R. Van Handel, Ben Adams, John S. Evseenko, Denis |
author_sort | Wu, Ling |
collection | PubMed |
description | Joint injury and osteoarthritis affect millions of people worldwide, but attempts to generate articular cartilage using adult stem/progenitor cells have been unsuccessful. We hypothesized that recapitulation of the human developmental chondrogenic program using pluripotent stem cells (PSCs) may represent a superior approach for cartilage restoration. Using laser-capture microdissection followed by microarray analysis, we first defined a surface phenotype (CD166(low/neg)CD146(low/neg)CD73(+)CD44(low)BMPR1B(+)) distinguishing the earliest cartilage committed cells (prechondrocytes) at 5–6 weeks of development. Functional studies confirmed these cells are chondrocyte progenitors. From 12 weeks, only the superficial layers of articular cartilage were enriched in cells with this progenitor phenotype. Isolation of cells with a similar immunophenotype from differentiating human PSCs revealed a population of CD166(low/neg)BMPR1B(+) putative cartilage-committed progenitors. Taken as a whole, these data define a developmental approach for the generation of highly purified functional human chondrocytes from PSCs that could enable substantial progress in cartilage tissue engineering. |
format | Online Article Text |
id | pubmed-3871393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-38713932013-12-26 Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells Wu, Ling Bluguermann, Carolina Kyupelyan, Levon Latour, Brooke Gonzalez, Stephanie Shah, Saumya Galic, Zoran Ge, Sundi Zhu, Yuhua Petrigliano, Frank A. Nsair, Ali Miriuka, Santiago G. Li, Xinmin Lyons, Karen M. Crooks, Gay M. McAllister, David R. Van Handel, Ben Adams, John S. Evseenko, Denis Stem Cell Reports Article Joint injury and osteoarthritis affect millions of people worldwide, but attempts to generate articular cartilage using adult stem/progenitor cells have been unsuccessful. We hypothesized that recapitulation of the human developmental chondrogenic program using pluripotent stem cells (PSCs) may represent a superior approach for cartilage restoration. Using laser-capture microdissection followed by microarray analysis, we first defined a surface phenotype (CD166(low/neg)CD146(low/neg)CD73(+)CD44(low)BMPR1B(+)) distinguishing the earliest cartilage committed cells (prechondrocytes) at 5–6 weeks of development. Functional studies confirmed these cells are chondrocyte progenitors. From 12 weeks, only the superficial layers of articular cartilage were enriched in cells with this progenitor phenotype. Isolation of cells with a similar immunophenotype from differentiating human PSCs revealed a population of CD166(low/neg)BMPR1B(+) putative cartilage-committed progenitors. Taken as a whole, these data define a developmental approach for the generation of highly purified functional human chondrocytes from PSCs that could enable substantial progress in cartilage tissue engineering. Elsevier 2013-12-12 /pmc/articles/PMC3871393/ /pubmed/24371811 http://dx.doi.org/10.1016/j.stemcr.2013.10.012 Text en © 2013 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-No Derivative Works License, which permits non-commercial use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Wu, Ling Bluguermann, Carolina Kyupelyan, Levon Latour, Brooke Gonzalez, Stephanie Shah, Saumya Galic, Zoran Ge, Sundi Zhu, Yuhua Petrigliano, Frank A. Nsair, Ali Miriuka, Santiago G. Li, Xinmin Lyons, Karen M. Crooks, Gay M. McAllister, David R. Van Handel, Ben Adams, John S. Evseenko, Denis Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells |
title | Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells |
title_full | Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells |
title_fullStr | Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells |
title_full_unstemmed | Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells |
title_short | Human Developmental Chondrogenesis as a Basis for Engineering Chondrocytes from Pluripotent Stem Cells |
title_sort | human developmental chondrogenesis as a basis for engineering chondrocytes from pluripotent stem cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3871393/ https://www.ncbi.nlm.nih.gov/pubmed/24371811 http://dx.doi.org/10.1016/j.stemcr.2013.10.012 |
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