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Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture

Although being of utmost importance for human health and mobility, stem cell identity and hierarchical organization of musculoskeletal progenitors remain largely unexplored. Here, cells from E10.5, E12.5, and E15.5 murine limbs are analyzed by high throughput single‐cell RNA sequencing to illustrate...

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Detalles Bibliográficos
Autores principales: Yin, Zi, Lin, Junxin, Yan, Ruojin, Liu, Richun, Liu, Mengfei, Zhou, Bo, Zhou, Wenyan, An, Chengrui, Chen, Yangwu, Hu, Yejun, Fan, Chunmei, Zhao, Kun, Wu, Bingbing, Zou, Xiaohui, Zhang, Jin, El‐Hashash, Ahmed H., Chen, Xiao, Ouyang, Hongwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710003/
https://www.ncbi.nlm.nih.gov/pubmed/33304744
http://dx.doi.org/10.1002/advs.202000938
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author Yin, Zi
Lin, Junxin
Yan, Ruojin
Liu, Richun
Liu, Mengfei
Zhou, Bo
Zhou, Wenyan
An, Chengrui
Chen, Yangwu
Hu, Yejun
Fan, Chunmei
Zhao, Kun
Wu, Bingbing
Zou, Xiaohui
Zhang, Jin
El‐Hashash, Ahmed H.
Chen, Xiao
Ouyang, Hongwei
author_facet Yin, Zi
Lin, Junxin
Yan, Ruojin
Liu, Richun
Liu, Mengfei
Zhou, Bo
Zhou, Wenyan
An, Chengrui
Chen, Yangwu
Hu, Yejun
Fan, Chunmei
Zhao, Kun
Wu, Bingbing
Zou, Xiaohui
Zhang, Jin
El‐Hashash, Ahmed H.
Chen, Xiao
Ouyang, Hongwei
author_sort Yin, Zi
collection PubMed
description Although being of utmost importance for human health and mobility, stem cell identity and hierarchical organization of musculoskeletal progenitors remain largely unexplored. Here, cells from E10.5, E12.5, and E15.5 murine limbs are analyzed by high throughput single‐cell RNA sequencing to illustrate the cellular architecture during limb development. Single‐cell transcriptional profiling demonstrates the identity and differentiation architecture of musculoskeletal stem cells (MSSC), soft and hard tissue progenitors through expression pattern of musculoskeletal markers (scleraxis [Scx], Hoxd13, Sox9, and Col1a1). This is confirmed by genetic in vivo lineage tracing. Moreover, single‐cell analyses of Scx knockout mice tissues illustrates that Scx regulates MSSC self‐renewal and proliferation potential. A high‐throughput and low‐cost multi‐tissues RNA sequencing strategy further provides evidence that musculoskeletal system tissues, including muscle, bone, meniscus, and cartilage, are all abnormally developed in Scx knockout mice. These results establish the presence of an indispensable limb Scx+Hoxd13+ MSSC population and their differentiation into soft tissue progenitors (Scx+Col1a1+) and hard tissue progenitors (Scx+Sox9+). Collectively, this study paves the way for systematically decoding the complex molecular mechanisms and cellular programs of musculoskeletal tissues morphogenesis in limb development and regeneration.
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spelling pubmed-77100032020-12-09 Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture Yin, Zi Lin, Junxin Yan, Ruojin Liu, Richun Liu, Mengfei Zhou, Bo Zhou, Wenyan An, Chengrui Chen, Yangwu Hu, Yejun Fan, Chunmei Zhao, Kun Wu, Bingbing Zou, Xiaohui Zhang, Jin El‐Hashash, Ahmed H. Chen, Xiao Ouyang, Hongwei Adv Sci (Weinh) Full Papers Although being of utmost importance for human health and mobility, stem cell identity and hierarchical organization of musculoskeletal progenitors remain largely unexplored. Here, cells from E10.5, E12.5, and E15.5 murine limbs are analyzed by high throughput single‐cell RNA sequencing to illustrate the cellular architecture during limb development. Single‐cell transcriptional profiling demonstrates the identity and differentiation architecture of musculoskeletal stem cells (MSSC), soft and hard tissue progenitors through expression pattern of musculoskeletal markers (scleraxis [Scx], Hoxd13, Sox9, and Col1a1). This is confirmed by genetic in vivo lineage tracing. Moreover, single‐cell analyses of Scx knockout mice tissues illustrates that Scx regulates MSSC self‐renewal and proliferation potential. A high‐throughput and low‐cost multi‐tissues RNA sequencing strategy further provides evidence that musculoskeletal system tissues, including muscle, bone, meniscus, and cartilage, are all abnormally developed in Scx knockout mice. These results establish the presence of an indispensable limb Scx+Hoxd13+ MSSC population and their differentiation into soft tissue progenitors (Scx+Col1a1+) and hard tissue progenitors (Scx+Sox9+). Collectively, this study paves the way for systematically decoding the complex molecular mechanisms and cellular programs of musculoskeletal tissues morphogenesis in limb development and regeneration. John Wiley and Sons Inc. 2020-10-22 /pmc/articles/PMC7710003/ /pubmed/33304744 http://dx.doi.org/10.1002/advs.202000938 Text en © 2020 The Authors. Published by Wiley‐VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Yin, Zi
Lin, Junxin
Yan, Ruojin
Liu, Richun
Liu, Mengfei
Zhou, Bo
Zhou, Wenyan
An, Chengrui
Chen, Yangwu
Hu, Yejun
Fan, Chunmei
Zhao, Kun
Wu, Bingbing
Zou, Xiaohui
Zhang, Jin
El‐Hashash, Ahmed H.
Chen, Xiao
Ouyang, Hongwei
Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture
title Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture
title_full Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture
title_fullStr Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture
title_full_unstemmed Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture
title_short Atlas of Musculoskeletal Stem Cells with the Soft and Hard Tissue Differentiation Architecture
title_sort atlas of musculoskeletal stem cells with the soft and hard tissue differentiation architecture
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710003/
https://www.ncbi.nlm.nih.gov/pubmed/33304744
http://dx.doi.org/10.1002/advs.202000938
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