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  4. Mechanical Stretch Induces mTOR Recruitment and Activation at the Phosphatidic Acid-Enriched Macropinosome in Muscle Cell
 
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Mechanical Stretch Induces mTOR Recruitment and Activation at the Phosphatidic Acid-Enriched Macropinosome in Muscle Cell

Journal
Frontiers in cell and developmental biology
Journal Volume
7
Journal Issue
May
Date Issued
2019
Author(s)
Lin, Shan-Shan
YA-WEN LIU  
DOI
10.3389/fcell.2019.00078
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85066803733&doi=10.3389%2ffcell.2019.00078&partnerID=40&md5=f52dfa9e6800db474175956aab1fe508
https://scholars.lib.ntu.edu.tw/handle/123456789/416760
URL
https://api.elsevier.com/content/abstract/scopus_id/85066803733
Abstract
The mammalian target of rapamycin (mTOR) is an evolutionarily conserved kinase which assembles a signaling network that integrates diverse biochemical and mechanical cues to coordinate cell growth and proliferation. Mechanical load has been well-appreciated to induce mTOR activation that leads to skeletal muscle growth through phospholipase D (PLD) activity and phosphatidic acid (PA) production. While PA produced by PLD1 is critical for mTOR activation upon mitogenic stimulation at the lysosome, it is unclear where PA is produced upon mechanical stimulation in skeletal muscle. Here we report that membrane tension fluctuation induces the formation of PA-enriched macropinosome in mouse C2C12-derived myotube by either mechanical stretch or osmotic shock. The tension oscillation-induced PA is accumulated at the membrane of macropinosome, not the lysosome. Furthermore, mTOR is recruited to the PA-enriched macropinosome, and its downstream signaling is activated. Our findings reveal the underpinning of mechanical activation of mTOR signaling, and more importantly, the stretch-induced PA-macropinosome as a new platform for mTOR activation.
Subjects
exercise; mechanotransduction; membrane tension; phospholipase D; skeletal muscle
SDGs

[SDGs]SDG3

[SDGs]SDG6

Publisher
FRONTIERS MEDIA SA
Type
journal article

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