Remodeling the Integration of Lipid Metabolism Between Liver and Adipose Tissue by Dietary Methionine Restriction in Rats

Author:

Hasek Barbara E.1,Boudreau Anik1,Shin Jeho1,Feng Daorong2,Hulver Matthew3,Van Nancy T.1,Laque Amanda1,Stewart Laura K.1,Stone Kirsten P.1,Wanders Desiree1,Ghosh Sujoy4,Pessin Jeffrey E.2,Gettys Thomas W.1

Affiliation:

1. Laboratories of Nutrient Sensing and Adipocyte Signaling, Pennington Biomedical Research Center, Baton Rouge, Louisiana

2. Departments of Medicine and Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, New York

3. Department of Human Nutrition, Foods, and Exercise, Virginia Tech, Blacksburg, Virginia

4. Laboratory of Computational Biology, Pennington Biomedical Research Center, Baton Rouge, Louisiana.

Abstract

Dietary methionine restriction (MR) produces an integrated series of biochemical and physiological responses that improve biomarkers of metabolic health, limit fat accretion, and enhance insulin sensitivity. Using transcriptional profiling to guide tissue-specific evaluations of molecular responses to MR, we report that liver and adipose tissue are the primary targets of a transcriptional program that remodeled lipid metabolism in each tissue. The MR diet produced a coordinated downregulation of lipogenic genes in the liver, resulting in a corresponding reduction in the capacity of the liver to synthesize and export lipid. In contrast, the transcriptional response in white adipose tissue (WAT) involved a depot-specific induction of lipogenic and oxidative genes and a commensurate increase in capacity to synthesize and oxidize fatty acids. These responses were accompanied by a significant change in adipocyte morphology, with the MR diet reducing cell size and increasing mitochondrial density across all depots. The coordinated transcriptional remodeling of lipid metabolism between liver and WAT by dietary MR produced an overall reduction in circulating and tissue lipids and provides a potential mechanism for the increase in metabolic flexibility and enhanced insulin sensitivity produced by the diet.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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