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Reduced efficiency of sarcolipin-dependent respiration in myocytes from humans with severe obesity

OBJECTIVE: Sarcolipin (SLN) regulates muscle energy expenditure through its action on sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) pump. It is unknown whether SLN-dependent respiration has relevance to human obesity, but whole-transcriptome gene expression profiling revealed that SLN was more h...

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Detalles Bibliográficos
Autores principales: Paran, Christopher W., Verkerke, Anthony R.P., Heden, Timothy D., Park, Sanghee, Zou, Kai, Lawson, Heather A., Song, Haowei, Turk, John, Houmard, Joseph A., Funai, Katsuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483165/
https://www.ncbi.nlm.nih.gov/pubmed/25970801
http://dx.doi.org/10.1002/oby.21123
Descripción
Sumario:OBJECTIVE: Sarcolipin (SLN) regulates muscle energy expenditure through its action on sarco/endoplasmic reticulum Ca(2+)-ATPase (SERCA) pump. It is unknown whether SLN-dependent respiration has relevance to human obesity, but whole-transcriptome gene expression profiling revealed that SLN was more highly expressed in myocytes from individuals with severe obesity (OB) than in lean controls (LN). The purpose of this study was to examine SLN-dependent cellular respiratory rates in LN and OB human muscles. DESIGN AND METHODS: Primary myocytes were isolated from muscle biopsy from seven LN and OB Caucasian females. Cellular respiration was assessed with and without lentivirus-mediated SLN knockdown in LN and OB myocytes. RESULTS: SLN mRNA and protein abundance was greater in OB compared to LN cells. Despite elevated SLN levels in wildtype OB cells, respiratory rates among SLN-deficient cells were higher in OB compared to LN. Obesity-induced reduction in efficiency of SLN-dependent respiration was associated with altered SR phospholipidome. CONCLUSIONS: SLN-dependent respiration is reduced in muscles from humans with severe obesity compared to lean controls. Identification of molecular mechanism that affects SLN-efficiency might promote an increase in skeletal muscle energy expenditure.