Retinoic acid signalling in fibro/adipogenic progenitors robustly enhances muscle regeneration

被引:28
|
作者
Zhao, Liang [1 ,2 ]
Son, Jun Seok [1 ,2 ]
Wang, Bo [3 ]
Tian, Qiyu [1 ,2 ]
Chen, Yanting [1 ,2 ]
Liu, Xiangdong [1 ,2 ]
de Avila, Jeanene M. [1 ,2 ]
Zhu, Mei-Jun [4 ]
Du, Min [1 ,2 ]
机构
[1] Washington State Univ, Dept Anim Sci, Nutrigenom & Growth Biol Lab, Pullman, WA 99164 USA
[2] Washington State Univ, Sch Mol Biosci, Pullman, WA 99164 USA
[3] China Agr Univ, Coll Anim Sci & Technol, State Key Lab Anim Nutr, Beijing 100193, Peoples R China
[4] Washington State Univ, Sch Food Sci, Pullman, WA 99164 USA
来源
EBIOMEDICINE | 2020年 / 60卷
基金
美国国家卫生研究院;
关键词
Fibro/adipogenic progenitors; Retinoic acid signalling; Muscle regeneration; Fibrosis; Adipogenesis; Obesity; SKELETAL-MUSCLE; SATELLITE CELLS; INJURY; RECEPTOR; ADIPOGENESIS; RESIDENT; SUPPRESSION; MECHANISMS; INHIBITION; EXPRESSION;
D O I
10.1016/j.ebiom.2020.103020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: During muscle regeneration, excessive formation of adipogenic and fibrogenic tissues, from their respective fibro/adipogenic progenitors (FAPs), impairs functional recovery. Intrinsic mechanisms controlling the proliferation and differentiation of FAPs remain largely unexplored. Methods: Here, we investigated the role of retinoic acid (RA) signalling in regulating FAPs and the subsequent effects on muscle restoration from a cardiotoxin-induced injury. Blockage of retinoic acid receptor (RAR) signalling was achieved through dominant negative retinoic acid receptor alpha (RAR alpha 403) expression specific in PDGFR alpha+ FAPs in vivo and by BMS493 treatment in vitro. Effects of RAR-signalling on FAP cellularity and muscle regeneration were also investigated in a high-fat diet-induced obese mice model. Findings: Supplementation of RA increased the proliferation of FAPs during the early stages of regeneration while suppressing FAP differentiation and promoting apoptosis during the remodelling stage. Loss of RARsignalling caused ectopic adipogenic differentiation of FAPs and impaired muscle regeneration. Furthermore, obesity disrupted the cellular transition of FAPs and attenuated muscle regeneration. Supplementation of RA to obese mice not only rescued impaired muscle fibre regeneration, but also inhibited infiltration of fat and fibrotic tissues during muscle repair. These beneficial effects were abolished after blocking RAR-signalling in FAPs of obese mice. Interpretation: These data suggest that RAR-signalling in FAPs is a critical therapeutic target for suppressing differentiation of FAPs and facilitating the regeneration of muscle and other tissues. Funding: This study was supported by grants from the National Institutes of Health (R01-HD067449 and R21-AG049976) to M.D. (c) 2020 The Author(s). Published by Elsevier B.V. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/)
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页数:12
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