Sitosterol-containing lipoproteins trigger free sterol-induced caspase-independent death in ACAT-competent macrophages

J Biol Chem. 2006 Nov 3;281(44):33635-49. doi: 10.1074/jbc.M606339200. Epub 2006 Aug 24.

Abstract

Sitosterolemia is a disease characterized by very high levels of sitosterol and other plant sterols and premature atherothrombotic vascular disease. One theory holds that plant sterols can directly promote atherosclerosis, but the mechanism is not known. Unesterified, or "free," cholesterol (FC) is a potent inducer of macrophage death, which causes plaque necrosis, a precursor to atherothrombosis. FC-induced macrophage death, however, requires dysfunction of the sterol esterifying enzyme acyl-coenzyme A-cholesterol acyltransferase (ACAT), which likely occurs slowly during lesion progression. In contrast, plant sterols are relatively poorly esterified by ACAT, and so they may cause macrophage death and plaque necrosis in an accelerated manner. In support of this hypothesis, we show here that macrophages incubated with sitosterol-containing lipoproteins accumulate free sterols and undergo death in the absence of an ACAT inhibitor. As with FC loading, sitosterol-induced macrophage death requires sterol trafficking to the endoplasmic reticulum, and sitosterol-enriched endoplasmic reticulum membranes show evidence of membrane protein dysfunction. However, whereas FC induces caspase-dependent apoptosis through activation of the unfolded protein response and JNK, sitosterol-induced death is caspase-independent and involves neither the unfolded protein response nor JNK. Rather, cell death shows signs of necroptosis and autophagy and is suppressed by inhibitors of both processes. These data establish two new concepts. First, a relatively subtle change in sterol structure fundamentally alters the type of death program triggered in macrophages. Understanding the basis of this alteration should provide new insights into the molecular basis of death pathway signaling. Second, sitosterol-induced macrophage death does not require ACAT dysfunction and so may occur in an accelerated fashion. Pending future in vivo studies, this concept may provide at least one mechanism for accelerated plaque necrosis and atherothrombotic disease in patients with sitosterolemia.

Publication types

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

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Biological Transport
  • Caspases / metabolism
  • Cells, Cultured
  • Endoplasmic Reticulum / metabolism
  • Enzyme Inhibitors / pharmacology
  • Female
  • Imidazoles / pharmacology
  • Indoles / pharmacology
  • Intracellular Membranes / metabolism
  • Lipoproteins / metabolism
  • Lipoproteins / pharmacology*
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases / metabolism
  • Sitosterols / metabolism*
  • Sterol O-Acyltransferase / antagonists & inhibitors
  • Sterol O-Acyltransferase / metabolism*
  • Sterols / metabolism*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Enzyme Inhibitors
  • Imidazoles
  • Indoles
  • Lipoproteins
  • Sitosterols
  • Sterols
  • necrostatin-1
  • gamma-sitosterol
  • Sterol O-Acyltransferase
  • p38 Mitogen-Activated Protein Kinases
  • Caspases
  • Sarcoplasmic Reticulum Calcium-Transporting ATPases