再生(生物学)
车站3
生物
细胞生物学
纤维化
心肌细胞
炎症
免疫学
病理
信号转导
医学
作者
Han Zhu,Fang Xiao,Gang Wang,Xiuqing Wei,Lei Jiang,Yan Chen,Lin Zhu,Haixia Wang,Yarui Diao,Huating Wang,Nancy Y. Ip,Tom H. Cheung,Zhenguo Wu
出处
期刊:Cell Reports
[Cell Press]
日期:2016-08-01
卷期号:16 (8): 2102-2115
被引量:58
标识
DOI:10.1016/j.celrep.2016.07.041
摘要
Recent studies have shown that STAT3 negatively regulates the proliferation of muscle satellite cells (MuSCs) and injury-induced muscle regeneration. These studies have been largely based on STAT3 inhibitors, which may produce off-target effects and are not cell type-specific in vivo. Here, we examine the role of STAT3 in MuSCs using two different mouse models: a MuSC-specific Stat3 knockout line and a Stat3 (MuSC-specific)/dystrophin (Dmd) double knockout (dKO) line. Stat3−/− MuSCs from both mutant lines were defective in proliferation. Moreover, in both mutant strains, the MuSC pool shrank, and regeneration was compromised after injury, with defects more pronounced in dKO mice along with severe muscle inflammation and fibrosis. We analyzed the transcriptomes of MuSCs from dKO and Dmd−/− control mice and identified multiple STAT3 target genes, including Pax7. Collectively, our work reveals a critical role of STAT3 in adult MuSCs that regulates their self-renewal during injury-induced muscle regeneration.
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