Inhibition of a Golgi complex lysophospholipid acyltransferase induces membrane tubule formation and retrograde trafficking

Mol Biol Cell. 2003 Aug;14(8):3459-69. doi: 10.1091/mbc.e02-11-0711. Epub 2003 May 3.

Abstract

Recent studies have suggested that formation of Golgi membrane tubules involves the generation of membrane-associated lysophospholipids by a cytoplasmic Ca2+-independent phospholipase A2 (PLA2). Herein, we provide additional support for this idea by showing that inhibition of lysophospholipid reacylation by a novel Golgi-associated lysophosphatidylcholine acyltransferase (LPAT) induces the rapid tubulation of Golgi membranes, leading in their retrograde movement to the endoplasmic reticulum. Inhibition of the Golgi LPAT was achieved by 2,2-dimethyl-N-(2,4,6-trimethoxyphenyl)dodecanamide (CI-976), a previously characterized antagonist of acyl-CoA cholesterol acyltransferase. The effect of CI-976 was similar to that of brefeldin A, except that the coatomer subunit beta-COP remained on Golgi-derived membrane tubules. CI-976 also enhanced the cytosol-dependent formation of tubules from Golgi complexes in vitro and increased the levels of lysophosphatidylcholine in Golgi membranes. Moreover, preincubation of cells with PLA2 antagonists inhibited the ability of CI-976 to induce tubules. These results suggest that Golgi membrane tubule formation can result from increasing the content of lysophospholipids in membranes, either by stimulation of a PLA2 or by inhibition of an LPAT. These two opposing enzyme activities may help to coordinately regulate Golgi membrane shape and tubule formation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 1-Acylglycerophosphocholine O-Acyltransferase / antagonists & inhibitors
  • 1-Acylglycerophosphocholine O-Acyltransferase / metabolism*
  • Acylation
  • Anilides / pharmacology
  • Brefeldin A / pharmacology
  • Golgi Apparatus / enzymology*
  • HeLa Cells
  • Humans
  • Lysophosphatidylcholines / metabolism
  • Phospholipases A / metabolism*
  • Phospholipases A2
  • Subcellular Fractions

Substances

  • Anilides
  • Lysophosphatidylcholines
  • PD 128042
  • Brefeldin A
  • 1-Acylglycerophosphocholine O-Acyltransferase
  • Phospholipases A
  • Phospholipases A2