Back to Search Start Over

Muscle Kruppel-like factor 15 regulates lipid flux and systemic metabolic homeostasis

Authors :
Fan, Liyan
Sweet, David R.
Prosdocimo, Domenick A.
Vinayachandran, Vinesh
Chan, Ernest R.
Zhang, Rongli
Ilkayeva, Olga
Lu, Yuan
Keerthy, Komal S.
Booth, Chloe E.
Newgard, Christopher B.
Jain, Mukesh K.
Source :
Journal of Clinical Investigation. April, 2021, Vol. 131 Issue 4
Publication Year :
2021

Abstract

Skeletal muscle is a major determinant of systemic metabolic homeostasis that plays a critical role in glucose metabolism and insulin sensitivity. By contrast, despite being a major user of fatty acids, and evidence that muscular disorders can lead to abnormal lipid deposition (e.g., nonalcoholic fatty liver disease in myopathies), our understanding of skeletal muscle regulation of systemic lipid homeostasis is not well understood. Here we show that skeletal muscle Kruppel-like factor 15 (KLF15) coordinates pathways central to systemic lipid homeostasis under basal conditions and in response to nutrient overload. Mice with skeletal muscle-specific KLF15 deletion demonstrated (a) reduced expression of key targets involved in lipid uptake, mitochondrial transport, and utilization, (b) elevated circulating lipids, (c) insulin resistance/glucose intolerance, and (d) increased lipid deposition in white adipose tissue and liver. Strikingly, a diet rich in short-chain fatty acids bypassed these defects in lipid flux and ameliorated aspects of metabolic dysregulation. Together, these findings establish skeletal muscle control of lipid flux as critical to systemic lipid homeostasis and metabolic health.<br />Introduction Beyond the structural and locomotive functions classically ascribed to skeletal muscle, this tissue represents the largest metabolic organ by mass and is a major site for the metabolism of [...]

Details

Language :
English
ISSN :
00219738
Volume :
131
Issue :
4
Database :
Gale General OneFile
Journal :
Journal of Clinical Investigation
Publication Type :
Academic Journal
Accession number :
edsgcl.652687379
Full Text :
https://doi.org/10.1172/JCI139496