期刊
JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE
卷 9, 期 5, 页码 947-961出版社
WILEY
DOI: 10.1002/jcsm.12319
关键词
Diaphragm; Denervation; Muscle stretch; Hypertrophy; Titin; Mechanosensing
资金
- National Institutes of Health [R01HL121500]
- MSCA-RISE-2014 project [645648]
- Foundation Leducq [13CVD04]
Background Titin is an elastic sarcomeric filament that has been proposed to play a key role in mechanosensing and trophicity of muscle. However, evidence for this proposal is scarce due to the lack of appropriate experimental models to directly test the role of titin in mechanosensing. Methods We used unilateral diaphragm denervation (UDD) in mice, an in vivo model in which the denervated hemidiaphragm is passively stretched by the contralateral, innervated hemidiaphragm and hypertrophy rapidly occurs. Results In wildtype mice, the denervated hemidiaphragm mass increased 48 +/- 3% after 6 days of UDD, due to the addition of both sarcomeres in series and in parallel. To test whether titin stiffness modulates the hypertrophy response, RBM20(Delta RRM) and Ttn(Delta IAjxn) mouse models were used, with decreased and increased titin stiffness, respectively. RBM20(Delta RRM) mice (reduced stiffness) showed a 20 +/- 6% attenuated hypertrophy response, whereas the Ttn(Delta IAjxn) mice (increased stiffness) showed an 18 +/- 8% exaggerated response after UDD. Thus, muscle hypertrophy scales with titin stiffness. Protein expression analysis revealed that titin-binding proteins implicated previously in muscle trophicity were induced during UDD, MARP1 & 2, FHL1, and MuRF1. Conclusions Titin functions as a mechanosensor that regulates muscle trophicity.
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