Nfix Regulates Temporal Progression of Muscle Regeneration through Modulation of Myostatin Expression

被引:61
|
作者
Rossi, Giuliana [1 ]
Antonini, Stefania [1 ]
Bonfanti, Chiara [1 ]
Monteverde, Stefania [1 ]
Vezzali, Chiara [1 ]
Tajbakhsh, Shahragim [2 ]
Cossu, Giulio [1 ,3 ]
Messina, Graziella [1 ]
机构
[1] Univ Milan, Dept Biosci, Via Celoria 26, I-20133 Milan, Italy
[2] Inst Pasteur, CNRS, Dept Dev & Stem Cell Biol, Stem Cells & Dev,UMR 3738, 25 Rue Dr Roux, F-75015 Paris, France
[3] Univ Manchester, Inst Inflammat & Repair, Oxford Rd, Manchester M13 9PL, Lancs, England
来源
CELL REPORTS | 2016年 / 14卷 / 09期
关键词
NUCLEAR-FACTOR-I; SKELETAL-MUSCLE; SATELLITE CELLS; DYSTROPHIC MUSCLE; SELF-RENEWAL; GENE; TRANSCRIPTION; ACTIVATION; PROTEIN; PROLIFERATION;
D O I
10.1016/j.celrep.2016.02.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nfix belongs to a family of four highly conserved proteins that act as transcriptional activators and/or repressors of cellular and viral genes. We previously showed a pivotal role for Nfix in regulating the transcriptional switch from embryonic to fetal myogenesis. Here, we show that Nfix directly represses the Myostatin promoter, thus controlling the proper timing of satellite cell differentiation and muscle regeneration. Nfix-null mice display delayed regeneration after injury, and this deficit is reversed upon in vivo Myostatin silencing. Conditional deletion of Nfix in satellite cells results in a similar delay in regeneration, confirming the functional requirement for Nfix in satellite cells. Moreover, mice lacking Nfix show reduced myofiber cross sectional area and a predominant slow twitching phenotype. These data define a role for Nfix in postnatal skeletal muscle and unveil a mechanism for Myostatin regulation, thus providing insights into the modulation of its complex signaling pathway.
引用
收藏
页码:2238 / 2249
页数:12
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