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Muscle Krüppel-like factor 15 regulates lipid flux and systemic metabolic homeostasis
Liyan Fan, … , Christopher B. Newgard, Mukesh K. Jain
Liyan Fan, … , Christopher B. Newgard, Mukesh K. Jain
Published February 15, 2021
Citation Information: J Clin Invest. 2021;131(4):e139496. https://doi.org/10.1172/JCI139496.
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Concise Communication Metabolism Muscle biology Article has an altmetric score of 78

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

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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 Krüppel-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.

Authors

Liyan Fan, David R. Sweet, Domenick A. Prosdocimo, Vinesh Vinayachandran, Ernest R. Chan, Rongli Zhang, Olga Ilkayeva, Yuan Lu, Komal S. Keerthy, Chloe E. Booth, Christopher B. Newgard, Mukesh K. Jain

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Figure 3

Skeletal muscle KLF15 is a major regulator of lipid flux pathways.

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Skeletal muscle KLF15 is a major regulator of lipid flux pathways.
(A) H...
(A) Heatmap clustering of 496 differentially enriched genes found in RNA sequencing of soleus muscle (n = 4). (B) Gene-set enrichment analysis using Gene Ontology Biological Processes showing the top 20 most significantly enriched pathways. (C) qPCR of select lipid flux pathway genes in soleus (n = 3–7). (D) Acylcarnitine analysis in soleus by tandem mass spectrometry. Data normalized to control group average for each acylcarnitine species and significantly different species (P < 0.05) are shown (n = 6–9). (E) Metabolic cage respiratory exchange quotient (RER) (n = 8–9). (F) Schematic representation of lipid flux pathway and defects seen in K15-SKO mice. Data represent mean ± SEM. Comparisons between MyoCre and K15-SKO mice were performed using an unpaired, 2-tailed Student’s t test, *P < 0.05, **P < 0.01, ***P < 0.001.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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