The emerging roles of lipids in circadian control

Biochim Biophys Acta. 2015 Aug;1851(8):1017-25. doi: 10.1016/j.bbalip.2014.11.013. Epub 2014 Dec 4.

Abstract

Lipids play vital roles in a wide variety of cellular functions. They act as structural components in cell membranes, serve as a major form of energy storage, and function as key signaling molecules. Mounting evidence points towards a tight interplay between lipids and circadian clocks. In mammals, circadian clocks regulate the daily physiology and metabolism, and disruption of circadian rhythmicity is associated with altered lipid homeostasis and pathologies such as fatty liver and obesity. Concomitantly, emerging evidence suggest that lipids are embedded within the core clock circuitry and participate in circadian control. Recent advances in lipidomics methodologies and their application in chronobiology studies have shed new light on the cross talk between circadian clocks and lipid homeostasis. We review herein the latest literature related to the involvement of lipids in circadian clock's function and highlight the contribution of circadian lipidomics studies to our understanding of circadian rhythmicity and lipid homeostasis. This article is part of a Special Issue entitled Brain Lipids.

Keywords: Circadian; Clocks; Lipidomics; Lipids; Metabolomics; Nutrition.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • CLOCK Proteins / genetics
  • CLOCK Proteins / metabolism
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Circadian Clocks / genetics*
  • Circadian Rhythm / genetics*
  • Fatty Liver / genetics
  • Fatty Liver / metabolism*
  • Fatty Liver / pathology
  • Gene Expression Regulation
  • Homeostasis
  • Humans
  • Lipid Metabolism / genetics*
  • Lipids / chemistry
  • Obesity / genetics
  • Obesity / metabolism*
  • Obesity / pathology
  • Peroxisome Proliferator-Activated Receptors / genetics
  • Peroxisome Proliferator-Activated Receptors / metabolism
  • Receptors, Retinoic Acid / genetics
  • Receptors, Retinoic Acid / metabolism
  • Signal Transduction

Substances

  • Lipids
  • Peroxisome Proliferator-Activated Receptors
  • Receptors, Retinoic Acid
  • CLOCK Proteins