Synthesis and function of hepatic very-low-density lipoprotein

Biochem Soc Trans. 2004 Feb;32(Pt 1):59-64. doi: 10.1042/bst0320059.

Abstract

Most of the triacylglycerol (TAG) utilized for the assembly of very-low-density lipoprotein (VLDL) in the secretory apparatus of the hepatocyte is mobilized by lipolysis of the cytosolic TAG pool, followed by re-esterification. The lipases involved include arylacetamide deacetylase and/or triacylglycerol hydrolase. Some of the re-esterified products of lipolysis gain access to an apolipoprotein-B-rich VLDL precursor to form mature VLDL. Some, however, are returned to the cytosolic pool in a process that is stimulated by insulin and inhibited by microsomal triacylglycerol transfer protein (MTP). Phospholipids also contribute to VLDL TAG in a process which involves ADP-ribosylation factor-1 (ARF-1)-mediated activation of phospholipase D. The temporary storage of TAG in the liver, followed by its mobilization and secretion as VLDL, form part of a process by which the liver protects vulnerable body tissues from excess lipotoxic non-esterified ('free') fatty acids in the plasma.

Publication types

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

MeSH terms

  • Animals
  • Apolipoproteins B / metabolism
  • Humans
  • Lipoproteins, VLDL / biosynthesis*
  • Lipoproteins, VLDL / metabolism*
  • Liver / metabolism*
  • Particle Size
  • Triglycerides / metabolism

Substances

  • Apolipoproteins B
  • Lipoproteins, VLDL
  • Triglycerides