The mitochondrial multi-omic response to exercise training across rat tissues

大鼠组织中线粒体多组学对运动训练的反应

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作者:David Amar ,Nicole R Gay ,David Jimenez-Morales ,Pierre M Jean Beltran ,Megan E Ramaker ,Archana Natarajan Raja ,Bingqing Zhao ,Yifei Sun ,Shruti Marwaha ,David A Gaul ,Steven G Hershman ,Alexis Ferrasse ,Ashley Xia ,Ian Lanza ,Facundo M Fernández ,Stephen B Montgomery ,Andrea L Hevener ,Euan A Ashley ,Martin J Walsh ,Lauren M Sparks ,Charles F Burant ,R Scott Rector ,John Thyfault ,Matthew T Wheeler ,Bret H Goodpaster ,Paul M Coen ,Simon Schenk ,Sue C Bodine ,Malene E Lindholm

Abstract

Mitochondria have diverse functions critical to whole-body metabolic homeostasis. Endurance training alters mitochondrial activity, but systematic characterization of these adaptations is lacking. Here, the Molecular Transducers of Physical Activity Consortium mapped the temporal, multi-omic changes in mitochondrial analytes across 19 tissues in male and female rats trained for 1, 2, 4, or 8 weeks. Training elicited substantial changes in the adrenal gland, brown adipose, colon, heart, and skeletal muscle. The colon showed non-linear response dynamics, whereas mitochondrial pathways were downregulated in brown adipose and adrenal tissues. Protein acetylation increased in the liver, with a shift in lipid metabolism, whereas oxidative proteins increased in striated muscles. Exercise-upregulated networks were downregulated in human diabetes and cirrhosis. Knockdown of the central network protein 17-beta-hydroxysteroid dehydrogenase 10 (HSD17B10) elevated oxygen consumption, indicative of metabolic stress. We provide a multi-omic, multi-tissue, temporal atlas of the mitochondrial response to exercise training and identify candidates linked to mitochondrial dysfunction. Keywords: HSD17B10; acetylome; aerobic; exercise; metabolism; metabolomics; mitochondria; multi-omics; proteomics; transcriptomics.

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