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Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality

The repair of injured tendons remains a formidable clinical challenge because of our limited understanding of tendon stem cells and the regulation of tenogenesis. With single-cell analysis to characterize the gene expression profiles of individual cells isolated from tendon tissue, a subpopulation o...

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Autores principales: Yin, Zi, Hu, Jia-jie, Yang, Long, Zheng, Ze-Feng, An, Cheng-rui, Wu, Bing-bing, Zhang, Can, Shen, Wei-Liang, Liu, Huan-huan, Chen, Jia-lin, Heng, Boon Chin, Guo, Guo-ji, Chen, Xiao, Ouyang, Hong-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5262457/
https://www.ncbi.nlm.nih.gov/pubmed/28138519
http://dx.doi.org/10.1126/sciadv.1600874
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author Yin, Zi
Hu, Jia-jie
Yang, Long
Zheng, Ze-Feng
An, Cheng-rui
Wu, Bing-bing
Zhang, Can
Shen, Wei-Liang
Liu, Huan-huan
Chen, Jia-lin
Heng, Boon Chin
Guo, Guo-ji
Chen, Xiao
Ouyang, Hong-Wei
author_facet Yin, Zi
Hu, Jia-jie
Yang, Long
Zheng, Ze-Feng
An, Cheng-rui
Wu, Bing-bing
Zhang, Can
Shen, Wei-Liang
Liu, Huan-huan
Chen, Jia-lin
Heng, Boon Chin
Guo, Guo-ji
Chen, Xiao
Ouyang, Hong-Wei
author_sort Yin, Zi
collection PubMed
description The repair of injured tendons remains a formidable clinical challenge because of our limited understanding of tendon stem cells and the regulation of tenogenesis. With single-cell analysis to characterize the gene expression profiles of individual cells isolated from tendon tissue, a subpopulation of nestin(+) tendon stem/progenitor cells (TSPCs) was identified within the tendon cell population. Using Gene Expression Omnibus datasets and immunofluorescence assays, we found that nestin expression was activated at specific stages of tendon development. Moreover, isolated nestin(+) TSPCs exhibited superior tenogenic capacity compared to nestin(−) TSPCs. Knockdown of nestin expression in TSPCs suppressed their clonogenic capacity and reduced their tenogenic potential significantly both in vitro and in vivo. Hence, these findings provide new insights into the identification of subpopulations of TSPCs and illustrate the crucial roles of nestin in TSPC fate decisions and phenotype maintenance, which may assist in future therapeutic strategies to treat tendon disease.
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spelling pubmed-52624572017-01-30 Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality Yin, Zi Hu, Jia-jie Yang, Long Zheng, Ze-Feng An, Cheng-rui Wu, Bing-bing Zhang, Can Shen, Wei-Liang Liu, Huan-huan Chen, Jia-lin Heng, Boon Chin Guo, Guo-ji Chen, Xiao Ouyang, Hong-Wei Sci Adv Research Articles The repair of injured tendons remains a formidable clinical challenge because of our limited understanding of tendon stem cells and the regulation of tenogenesis. With single-cell analysis to characterize the gene expression profiles of individual cells isolated from tendon tissue, a subpopulation of nestin(+) tendon stem/progenitor cells (TSPCs) was identified within the tendon cell population. Using Gene Expression Omnibus datasets and immunofluorescence assays, we found that nestin expression was activated at specific stages of tendon development. Moreover, isolated nestin(+) TSPCs exhibited superior tenogenic capacity compared to nestin(−) TSPCs. Knockdown of nestin expression in TSPCs suppressed their clonogenic capacity and reduced their tenogenic potential significantly both in vitro and in vivo. Hence, these findings provide new insights into the identification of subpopulations of TSPCs and illustrate the crucial roles of nestin in TSPC fate decisions and phenotype maintenance, which may assist in future therapeutic strategies to treat tendon disease. American Association for the Advancement of Science 2016-11-18 /pmc/articles/PMC5262457/ /pubmed/28138519 http://dx.doi.org/10.1126/sciadv.1600874 Text en Copyright © 2016, The Authors http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Yin, Zi
Hu, Jia-jie
Yang, Long
Zheng, Ze-Feng
An, Cheng-rui
Wu, Bing-bing
Zhang, Can
Shen, Wei-Liang
Liu, Huan-huan
Chen, Jia-lin
Heng, Boon Chin
Guo, Guo-ji
Chen, Xiao
Ouyang, Hong-Wei
Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
title Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
title_full Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
title_fullStr Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
title_full_unstemmed Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
title_short Single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
title_sort single-cell analysis reveals a nestin(+) tendon stem/progenitor cell population with strong tenogenic potentiality
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5262457/
https://www.ncbi.nlm.nih.gov/pubmed/28138519
http://dx.doi.org/10.1126/sciadv.1600874
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