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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2013
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.
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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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