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Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1

Mechanical force regulates bone density, modeling, and homeostasis. Substantial periosteal bone formation is generated by external mechanical stimuli, yet its mechanism is poorly understood. Here, it is shown that myeloid‐lineage cells differentiate into subgroups and regulate periosteal bone format...

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Autores principales: Deng, Ruoxian, Li, Changwei, Wang, Xiao, Chang, Leilei, Ni, Shuangfei, Zhang, Weixin, Xue, Peng, Pan, Dayu, Wan, Mei, Deng, Lianfu, Cao, Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787385/
https://www.ncbi.nlm.nih.gov/pubmed/34854257
http://dx.doi.org/10.1002/advs.202103343
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author Deng, Ruoxian
Li, Changwei
Wang, Xiao
Chang, Leilei
Ni, Shuangfei
Zhang, Weixin
Xue, Peng
Pan, Dayu
Wan, Mei
Deng, Lianfu
Cao, Xu
author_facet Deng, Ruoxian
Li, Changwei
Wang, Xiao
Chang, Leilei
Ni, Shuangfei
Zhang, Weixin
Xue, Peng
Pan, Dayu
Wan, Mei
Deng, Lianfu
Cao, Xu
author_sort Deng, Ruoxian
collection PubMed
description Mechanical force regulates bone density, modeling, and homeostasis. Substantial periosteal bone formation is generated by external mechanical stimuli, yet its mechanism is poorly understood. Here, it is shown that myeloid‐lineage cells differentiate into subgroups and regulate periosteal bone formation in response to mechanical loading. Mechanical loading on tibiae significantly increases the number of periosteal myeloid‐lineage cells and the levels of active transforming growth factor β (TGF‐β), resulting in cortical bone formation. Knockout of Tgfb1 in myeloid‐lineage cells attenuates mechanical loading‐induced periosteal bone formation in mice. Moreover, CD68(+)F4/80(+) macrophages, a subtype of myeloid‐lineage cells, express and activate TGF‐β1 for recruitment of osteoprogenitors. Particularly, mechanical loading induces the differentiation of periosteal CD68(+)F4/80(−) myeloid‐lineage cells to the CD68(+)F4/80(+) macrophages via signaling of piezo‐type mechanosensitive ion channel component 1 (Piezo1) for TGF‐β1 secretion. Importantly, CD68(+)F4/80(+) macrophages activate TGF‐β1 by expression and secretion of thrombospondin‐1 (Thbs1). Administration of Thbs1 inhibitor significantly impairs loading‐induced TGF‐β activation and recruitment of osteoprogenitors in the periosteum. The results suggest that periosteal myeloid‐lineage cells respond to mechanical forces and consequently produce and activate TGF‐β1 for periosteal bone formation.
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spelling pubmed-87873852022-01-31 Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1 Deng, Ruoxian Li, Changwei Wang, Xiao Chang, Leilei Ni, Shuangfei Zhang, Weixin Xue, Peng Pan, Dayu Wan, Mei Deng, Lianfu Cao, Xu Adv Sci (Weinh) Research Articles Mechanical force regulates bone density, modeling, and homeostasis. Substantial periosteal bone formation is generated by external mechanical stimuli, yet its mechanism is poorly understood. Here, it is shown that myeloid‐lineage cells differentiate into subgroups and regulate periosteal bone formation in response to mechanical loading. Mechanical loading on tibiae significantly increases the number of periosteal myeloid‐lineage cells and the levels of active transforming growth factor β (TGF‐β), resulting in cortical bone formation. Knockout of Tgfb1 in myeloid‐lineage cells attenuates mechanical loading‐induced periosteal bone formation in mice. Moreover, CD68(+)F4/80(+) macrophages, a subtype of myeloid‐lineage cells, express and activate TGF‐β1 for recruitment of osteoprogenitors. Particularly, mechanical loading induces the differentiation of periosteal CD68(+)F4/80(−) myeloid‐lineage cells to the CD68(+)F4/80(+) macrophages via signaling of piezo‐type mechanosensitive ion channel component 1 (Piezo1) for TGF‐β1 secretion. Importantly, CD68(+)F4/80(+) macrophages activate TGF‐β1 by expression and secretion of thrombospondin‐1 (Thbs1). Administration of Thbs1 inhibitor significantly impairs loading‐induced TGF‐β activation and recruitment of osteoprogenitors in the periosteum. The results suggest that periosteal myeloid‐lineage cells respond to mechanical forces and consequently produce and activate TGF‐β1 for periosteal bone formation. John Wiley and Sons Inc. 2021-12-02 /pmc/articles/PMC8787385/ /pubmed/34854257 http://dx.doi.org/10.1002/advs.202103343 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Deng, Ruoxian
Li, Changwei
Wang, Xiao
Chang, Leilei
Ni, Shuangfei
Zhang, Weixin
Xue, Peng
Pan, Dayu
Wan, Mei
Deng, Lianfu
Cao, Xu
Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1
title Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1
title_full Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1
title_fullStr Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1
title_full_unstemmed Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1
title_short Periosteal CD68(+)F4/80(+) Macrophages Are Mechanosensitive for Cortical Bone Formation by Secretion and Activation of TGF‐β1
title_sort periosteal cd68(+)f4/80(+) macrophages are mechanosensitive for cortical bone formation by secretion and activation of tgf‐β1
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787385/
https://www.ncbi.nlm.nih.gov/pubmed/34854257
http://dx.doi.org/10.1002/advs.202103343
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