IRE1beta inhibits chylomicron production by selectively degrading MTP mRNA

Cell Metab. 2008 May;7(5):445-55. doi: 10.1016/j.cmet.2008.03.005.

Abstract

Microsomal triglyceride transfer protein (MTP) is needed to assemble chylomicrons in the endoplasmic reticulum (ER) of enterocytes. We explored the role of an ER stress protein, inositol-requiring enzyme 1beta (IRE1beta), in regulating this process. High-cholesterol and high-fat diets decreased intestinal IRE1beta mRNA in wild-type mice. Ire1b(-/-) mice fed high-cholesterol and high-fat diets developed more pronounced hyperlipidemia because these mice secreted more chylomicrons and expressed more intestinal MTP, though not hepatic MTP, than wild-type mice did. Chylomicron secretion and MTP expression also were increased in primary enterocytes isolated from cholesterol-fed Ire1b(-/-) mice. There was no correlation between ER stress and MTP expression. Instead, cell culture studies revealed that IRE1beta, but not its ubiquitous homolog IRE1alpha, decreased MTP mRNA through increased posttranscriptional degradation. Conversely, knockdown of IRE1beta enhanced MTP expression. These studies show that IRE1beta plays a role in regulating MTP and in chylomicron production.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Blotting, Western
  • Body Weight
  • Carrier Proteins / genetics*
  • Carrier Proteins / metabolism
  • Cholesterol / metabolism
  • Chylomicrons / metabolism*
  • Diet, Atherogenic
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum / pathology*
  • Enterocytes / cytology
  • Enterocytes / metabolism
  • Hyperlipidemias / etiology*
  • Intestinal Mucosa / metabolism
  • Intestinal Mucosa / pathology
  • Lipids / analysis
  • Male
  • Membrane Proteins / antagonists & inhibitors
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Membrane Transport Proteins
  • Mice
  • Mice, Knockout
  • Microsomes / metabolism
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • RNA Processing, Post-Transcriptional
  • RNA, Messenger / metabolism*
  • RNA, Small Interfering / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction

Substances

  • Carrier Proteins
  • Chylomicrons
  • Laptm4a protein, mouse
  • Lipids
  • Membrane Proteins
  • Membrane Transport Proteins
  • RNA, Messenger
  • RNA, Small Interfering
  • microsomal triglyceride transfer protein
  • Cholesterol
  • Ern2 protein, mouse
  • Protein Serine-Threonine Kinases