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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Mitophagy protects against statin-mediated skeletal muscle toxicity

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Author(s):
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Ramesh, Mridula [1] ; Campos, Juliane C. [2, 3] ; Lee, Pamela [1] ; Song, Yang [3] ; Hernandez, Genaro [1] ; Sin, Jon [3] ; Tucker, Kyle C. [3] ; Saadaeijahromi, Hannaneh [3] ; Gurney, Michael [1] ; Ferreira, Julio C. B. [2] ; Andres, Allen M. [3]
Total Authors: 11
Affiliation:
[1] San Diego State Univ, Donald P Shiley BioSci Ctr, San Diego, CA 92182 - USA
[2] Univ Sao Paulo, Inst Biomed Sci, Sao Paulo - Brazil
[3] Cedars Sinai Med Ctr, Los Angeles, CA 90048 - USA
Total Affiliations: 3
Document type: Journal article
Source: FASEB JOURNAL; v. 33, n. 11, p. 11857-11869, NOV 2019.
Web of Science Citations: 0
Abstract

The deleterious effects of statins on skeletal muscle are well known, but the mechanism associated with these effects remains unresolved. Statins are associated with mitochondrial damage, which may contribute to muscle myopathy. Here we demonstrate that simvastatin induces mitophagy in skeletal muscle cells and hypothesized that attenuating this process by silencing the mitophagy adapter p62/sequestosome-1 (SQSTM1) might mitigate myotoxicity. Surprisingly, silencing p62/SQSTM1 in differentiated C2C12 muscle cells exacerbated rather than attenuated myotoxicity. This inhibition of mitophagy in the face of statin challenge correlated with increased release of cytochrome c to the cytosol, activation of caspase-3, and lactate dehydrogenase (LDH) release. Correspondingly, targeted knockdown of Parkin, a canonical E3 ubiquitin ligase important for mitophagy, mirrored the effects of p62/SQSTM1 silencing. To corroborate these findings in vivo, we treated Parkin knockout mice with simvastatin for 2 wk. In line with our findings in vitro, these mitophagy-compromised mice displayed reduced spontaneous activity, loss of grip strength, and increased circulating levels of muscle damage marker LDH. Our findings demonstrate that mitophagy is an important mechanism to resist statin-induced skeletal muscle damage. (AU)

FAPESP's process: 16/01633-5 - BETA2-ADRENOCEPTOR ACTIVATION COUNTERACTS SKELETAL MUSCLE WEAKNESS/WASTING: ROLE OF AUTOPHAGY
Grantee:Juliane Cruz Campos
Support Opportunities: Scholarships abroad - Research Internship - Doctorate