Depletion of TM6SF2 disturbs membrane lipid composition and dynamics in HuH7 hepatoma cells

Biochim Biophys Acta Mol Cell Biol Lipids. 2017 Jul;1862(7):676-685. doi: 10.1016/j.bbalip.2017.04.004. Epub 2017 Apr 18.

Abstract

A polymorphism of TM6SF2 associates with hepatic lipid accumulation and reduction of triacylglycerol (TAG) secretion, but the function of the encoded protein has remained enigmatic. We studied the effect of stable TM6SF2 knock-down on the lipid content and composition, mitochondrial fatty acid oxidation and organelle structure of HuH7 hepatoma cells. Knock-down of TM6SF2 resulted in intracellular accumulation of TAGs, cholesterol esters, phosphatidylcholine (PC) and phosphatidylethanolamine. In all of these lipid classes, polyunsaturated lipid species were significantly reduced while saturated and monounsaturated species increased their proportions. The PCs encountered relative and absolute arachidonic acid (AA, 20:4n-6) depletion, and AA was also reduced in the total cellular fatty acid pool. Synthesis and turnover of the hepatocellular glycerolipids was enhanced. The TM6SF2 knock-down cells secreted lipoprotein-like particles with a smaller diameter than in the controls, and more lysosome/endosome structures appeared in the knock-down cells. The mitochondrial capacity for palmitate oxidation was significantly reduced. These observations provide novel clues to TM6SF2 function and raise altered mebrane lipid composition and dynamics among the mechanism(s) by which the protein deficiency disturbs hepatic TAG secretion.

Keywords: Arachidonic acid; Fatty acid oxidation; Lipidome; Phosphatidylcholine; TM6SF2; Triacylglycerol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arachidonic Acid / metabolism
  • Carcinoma, Hepatocellular / genetics*
  • Carcinoma, Hepatocellular / metabolism*
  • Cell Line, Tumor
  • Cholesterol Esters / metabolism
  • Endosomes / metabolism
  • Fatty Acids / metabolism
  • Gene Knockdown Techniques / methods
  • Hepatocytes / metabolism
  • Humans
  • Lipid Metabolism / genetics
  • Lipoproteins / metabolism
  • Liver Neoplasms / genetics*
  • Liver Neoplasms / metabolism*
  • Lysosomes / metabolism
  • Membrane Lipids / metabolism*
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Oxidation-Reduction
  • Phosphatidylcholines / metabolism
  • Phosphatidylethanolamines / metabolism
  • Triglycerides / metabolism

Substances

  • Cholesterol Esters
  • Fatty Acids
  • Lipoproteins
  • Membrane Lipids
  • Membrane Proteins
  • Phosphatidylcholines
  • Phosphatidylethanolamines
  • TM6SF2 protein, human
  • Triglycerides
  • Arachidonic Acid
  • phosphatidylethanolamine