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 Ca2+‐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 high...

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Published inObesity (Silver Spring, Md.) Vol. 23; no. 7; pp. 1440 - 1449
Main Authors 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
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.07.2015
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ISSN1930-7381
1930-739X
1930-739X
DOI10.1002/oby.21123

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Summary:Objective Sarcolipin (SLN) regulates muscle energy expenditure through its action on sarco/endoplasmic reticulum Ca2+‐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. 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 wild‐type 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 sarcoplasmic reticulum phospholipidome. Conclusions SLN‐dependent respiration is reduced in muscles from humans with severe obesity compared to lean controls. Identification of the molecular mechanism that affects SLN efficiency might lead to interventions that promote an increase in skeletal muscle energy expenditure.
Bibliography:CWP and KF conceived the experiments. CWP, ARPV, and TDH conducted cell culture, gene expression, and respiratory measurements. CWP and HAL contributed to RNAseq experiments. KZ and SP contributed to fatty acid oxidation measurements. HS and JT conducted lipidomics experiments. TDH, KZ, SP, JAH, and KF conducted the clinical study. ARPV and KF wrote the manuscript. All contributed to manuscript edits.
This work was funded by East Carolina University startup fund and by NIH grants DK095774 to K.F., DK095003 to H.A.L., and DK056112 to J.A.H. The Washington University Medicine Department Mass Spectrometry Facility is supported by United States Public Health Service Grants P41‐GM103422, P60‐DK20579, and P30‐DK56341.
The authors declared no conflict of interest.
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ISSN:1930-7381
1930-739X
1930-739X
DOI:10.1002/oby.21123