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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2016
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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. |
format | Online Article Text |
id | pubmed-5262457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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