A Diet-Sensitive BAF60a-Mediated Pathway Links Hepatic Bile Acid Metabolism to Cholesterol Absorption and Atherosclerosis

Cell Rep. 2015 Nov 24;13(8):1658-69. doi: 10.1016/j.celrep.2015.10.033. Epub 2015 Nov 12.

Abstract

Dietary nutrients interact with gene networks to orchestrate adaptive responses during metabolic stress. Here, we identify Baf60a as a diet-sensitive subunit of the SWI/SNF chromatin-remodeling complexes in the mouse liver that links the consumption of fat- and cholesterol-rich diet to elevated plasma cholesterol levels. Baf60a expression was elevated in the liver following feeding with a western diet. Hepatocyte-specific inactivation of Baf60a reduced bile acid production and cholesterol absorption, and attenuated diet-induced hypercholesterolemia and atherosclerosis in mice. Baf60a stimulates expression of genes involved in bile acid synthesis, modification, and transport through a CAR/Baf60a feedforward regulatory loop. Baf60a is required for the recruitment of the SWI/SNF chromatin-remodeling complexes to facilitate an activating epigenetic switch on target genes. These studies elucidate a regulatory pathway that mediates the hyperlipidemic and atherogenic effects of western diet consumption.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atherosclerosis / metabolism*
  • Bile Acids and Salts / metabolism*
  • Cholesterol / metabolism*
  • Chromatin Assembly and Disassembly / physiology
  • Chromosomal Proteins, Non-Histone / metabolism*
  • Diet / methods
  • Hepatocytes / metabolism
  • Lipid Metabolism / physiology
  • Liver / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout

Substances

  • Bile Acids and Salts
  • Chromosomal Proteins, Non-Histone
  • Smarcd1 protein, mouse
  • Cholesterol

Associated data

  • GEO/GSE73709