Irgm1 knockout indirectly inhibits regeneration after skeletal muscle injury in mice

•Irgm1−/− mice showed poor and delayed skeletal muscle injury repair.•Irgm1 knockout did not affect myoblast differentiation in vitro.•Irgm1−/− increased the levels of IFN-γ to suppress myoblast differentiation in vivo. Immunity-related GTPase family M1 protein (lRGM1) plays an important role in hos...

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Veröffentlicht in:International immunopharmacology 2020-07, Vol.84, p.106515-106515, Article 106515
Hauptverfasser: Zhang, Liulei, Wang, Guangyou, Chen, Xin, Zhang, Chong, Jiang, Yan, Zhao, Wei, Li, Hulun, Sun, Jin, Li, Xinrong, Xu, Hao, Weng, Yuting, Zhang, Xiaoyu, Hou, Lixuan, Kong, Qingfei, Liu, Yumei, Xu, Hongwei, Mu, Lili, Wang, Jinghua
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container_title International immunopharmacology
container_volume 84
creator Zhang, Liulei
Wang, Guangyou
Chen, Xin
Zhang, Chong
Jiang, Yan
Zhao, Wei
Li, Hulun
Sun, Jin
Li, Xinrong
Xu, Hao
Weng, Yuting
Zhang, Xiaoyu
Hou, Lixuan
Kong, Qingfei
Liu, Yumei
Xu, Hongwei
Mu, Lili
Wang, Jinghua
description •Irgm1−/− mice showed poor and delayed skeletal muscle injury repair.•Irgm1 knockout did not affect myoblast differentiation in vitro.•Irgm1−/− increased the levels of IFN-γ to suppress myoblast differentiation in vivo. Immunity-related GTPase family M1 protein (lRGM1) plays an important role in host resistance to infection, immune inflammation, and tumors, and it is expressed in various tissues and cells, including the central nervous system, cardiovascular system, bone marrow-derived cells, glioma, and melanoma. However, the effect of IRGM1 in the muscles has not been reported to date. In this study, Irgm1−/− mice were used to evaluate the effect of lrgm1 on regeneration after skeletal muscle injury. The tibialis anterior muscle in Irgm1−/− mice was poorly repaired after BaCl2-induced injury, whereas lrgm1 knockout itself had no significant effect on the differentiation of myoblasts. However, the microenvironment of Irgm1−/− mice with a high interferon-gamma level inhibited the differentiation of myoblasts in vivo. These results suggest that lrgm1 knockout indirectly inhibits skeletal muscle regeneration after injury, providing new insights into the biological function of IRGM1.
doi_str_mv 10.1016/j.intimp.2020.106515
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Immunity-related GTPase family M1 protein (lRGM1) plays an important role in host resistance to infection, immune inflammation, and tumors, and it is expressed in various tissues and cells, including the central nervous system, cardiovascular system, bone marrow-derived cells, glioma, and melanoma. However, the effect of IRGM1 in the muscles has not been reported to date. In this study, Irgm1−/− mice were used to evaluate the effect of lrgm1 on regeneration after skeletal muscle injury. The tibialis anterior muscle in Irgm1−/− mice was poorly repaired after BaCl2-induced injury, whereas lrgm1 knockout itself had no significant effect on the differentiation of myoblasts. However, the microenvironment of Irgm1−/− mice with a high interferon-gamma level inhibited the differentiation of myoblasts in vivo. These results suggest that lrgm1 knockout indirectly inhibits skeletal muscle regeneration after injury, providing new insights into the biological function of IRGM1.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32311672</pmid><doi>10.1016/j.intimp.2020.106515</doi><tpages>1</tpages></addata></record>
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subjects Animals
Barium chloride
Barium Compounds
Bone marrow
Brain tumors
Cardiovascular system
Cell Differentiation
Cells, Cultured
Central nervous system
Chlorides
Differentiation
Glioma cells
GTP-Binding Proteins - genetics
GTP-Binding Proteins - physiology
Injuries
Interferon
Interferon-gamma - physiology
lrgm1
Male
Melanoma
Mice, Knockout
Microenvironment
Muscle regeneration
Muscle, Skeletal - injuries
Muscle, Skeletal - physiology
Muscles
Musculoskeletal system
Myoblasts
Regeneration
Satellite Cells, Skeletal Muscle - physiology
Skeletal muscle
Skeletal muscle injury
Tibialis anterior muscle
Tumors
γ-Interferon
title Irgm1 knockout indirectly inhibits regeneration after skeletal muscle injury in mice
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