Cell Metabolism
Volume 12, Issue 2, 4 August 2010, Pages 187-193
Journal home page for Cell Metabolism

Short Article
Intestinal Specific LXR Activation Stimulates Reverse Cholesterol Transport and Protects from Atherosclerosis

https://doi.org/10.1016/j.cmet.2010.07.002Get rights and content
Under an Elsevier user license
open archive

Summary

Several steps of the HDL-mediated reverse cholesterol transport (RCT) are transcriptionally regulated by the nuclear receptors LXRs in the macrophages, liver, and intestine. Systemic LXR activation via synthetic ligands induces RCT but also causes increased hepatic fatty acid synthesis and steatosis, limiting the potential therapeutic use of LXR agonists. During the last few years, the participation of the intestine in the control of RCT has appeared more evident. Here we show that while hepatic-specific LXR activation does not contribute to RCT, intestinal-specific LXR activation leads to decreased intestinal cholesterol absorption, improved lipoprotein profile, and increased RCT in vivo in the absence of hepatic steatosis. These events protect against atherosclerosis in the background of the LDLR-deficient mice. Our study fully characterizes the molecular and metabolic scenario that elects the intestine as a key player in the LXR-driven protective environment against cardiovascular disease.

Highlights

► Intestinal-specific LXR activation increases preβ-HDL cholesterol and induces RCT ► Hepatic-specific LXR activation does not contribute to RCT ► Intestinal-specific LXR activation prevents diet-induced hepatic lipogenesis and fatty liver ► Intestinal-specific LXR activation protects from atherosclerosis in the LDLR−/− mice

HUMDISEASE
SIGNALING

Cited by (0)