Cytosolic lipid droplets: from mechanisms of fat storage to disease

Crit Rev Biochem Mol Biol. 2014 Jul-Aug;49(4):304-26. doi: 10.3109/10409238.2014.931337.

Abstract

The lipid droplet (LD) is a phylogenetically conserved organelle. In eukaryotes, it is born from the endoplasmic reticulum, but unlike its parent organelle, LDs are the only known cytosolic organelles that are micellar in structure. LDs are implicated in numerous physiological and pathophysiological functions. Many aspects of the LD has captured the attention of diverse scientists alike and has recently led to an explosion in information on the LD biogenesis, expansion and fusion, identification of LD proteomes and diseases associated with LD biology. This review will provide a brief history of this fascinating organelle and provide some contemporary views of unanswered questions in LD biogenesis.

Keywords: Adipose; diabetes; endoplasmic reticulum; evolution; lipid droplets; lipodystrophy; phospholipid; triglyceride.

Publication types

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

MeSH terms

  • Animals
  • Carboxylic Ester Hydrolases / metabolism
  • Carrier Proteins / metabolism
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum / pathology
  • Humans
  • Lipid Droplets / chemistry
  • Lipid Droplets / enzymology
  • Lipid Droplets / metabolism*
  • Lipid Droplets / pathology*
  • Lipid Metabolism Disorders / metabolism*
  • Lipid Metabolism Disorders / pathology
  • Lipid Metabolism*
  • Perilipin-1
  • Phosphoproteins / metabolism

Substances

  • Carrier Proteins
  • Perilipin-1
  • Phosphoproteins
  • Carboxylic Ester Hydrolases