Free cholesterol accumulation in macrophage membranes activates Toll-like receptors and p38 mitogen-activated protein kinase and induces cathepsin K

Circ Res. 2009 Feb 27;104(4):455-65. doi: 10.1161/CIRCRESAHA.108.182568. Epub 2009 Jan 2.

Abstract

The molecular events linking lipid accumulation in atherosclerotic plaques to complications such as aneurysm formation and plaque disruption are poorly understood. BALB/c-Apoe(-/-) mice bearing a null mutation in the Npc1 gene display prominent medial erosion and atherothrombosis, whereas their macrophages accumulate free cholesterol in late endosomes and show increased cathepsin K (Ctsk) expression. We now show increased cathepsin K immunostaining and increased cysteinyl proteinase activity using near infrared fluorescence imaging over proximal aortas of Apoe(-/-), Npc1(-/-) mice. In mechanistic studies, cholesterol loading of macrophage plasma membranes (cyclodextrin-cholesterol) or endosomal system (AcLDL+U18666A or Npc1 null mutation) activated Toll-like receptor (TLR) signaling, leading to sustained phosphorylation of p38 mitogen-activated protein kinase and induction of p38 targets, including Ctsk, S100a8, Mmp8, and Mmp14. Studies in macrophages from knockout mice showed major roles for TLR4, following plasma membrane cholesterol loading, and for TLR3, after late endosomal loading. TLR signaling via p38 led to phosphorylation and activation of the transcription factor Microphthalmia transcription factor, acting at E-box elements in the Ctsk promoter. These studies suggest that free cholesterol enrichment of either plasma or endosomal membranes in macrophages leads to activation of signaling via various TLRs, prolonged p38 mitogen-activated protein kinase activation, and induction of Mmps, Ctsk, and S100a8, potentially contributing to plaque complications.

Publication types

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

MeSH terms

  • Adaptor Proteins, Vesicular Transport / deficiency
  • Adaptor Proteins, Vesicular Transport / genetics
  • Animals
  • Aorta / metabolism
  • Apolipoproteins E / deficiency
  • Apolipoproteins E / genetics
  • Calgranulin A
  • Cathepsin K
  • Cathepsins / biosynthesis*
  • Cell Membrane / enzymology
  • Cell Membrane / immunology
  • Cell Membrane / metabolism*
  • Cells, Cultured
  • Cholesterol / metabolism*
  • E-Box Elements
  • Endosomes / enzymology
  • Endosomes / immunology
  • Endosomes / metabolism*
  • Enzyme Induction
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Macrophages / enzymology
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Matrix Metalloproteinase 14 / metabolism
  • Matrix Metalloproteinase 8 / metabolism
  • Mice
  • Mice, Inbred C3H
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Microphthalmia-Associated Transcription Factor / metabolism
  • Niemann-Pick C1 Protein
  • Phosphorylation
  • Promoter Regions, Genetic
  • Proteins / genetics
  • Proteins / metabolism
  • Receptor Activator of Nuclear Factor-kappa B / metabolism
  • S100 Proteins / metabolism
  • Signal Transduction*
  • Time Factors
  • Toll-Like Receptor 3 / deficiency
  • Toll-Like Receptor 3 / genetics
  • Toll-Like Receptor 3 / metabolism*
  • Toll-Like Receptor 4 / deficiency
  • Toll-Like Receptor 4 / genetics
  • Toll-Like Receptor 4 / metabolism*
  • p38 Mitogen-Activated Protein Kinases / deficiency
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism*
  • rab GTP-Binding Proteins / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Apolipoproteins E
  • Calgranulin A
  • Intracellular Signaling Peptides and Proteins
  • Microphthalmia-Associated Transcription Factor
  • Mitf protein, mouse
  • Mmp14 protein, mouse
  • Niemann-Pick C1 Protein
  • Npc1 protein, mouse
  • Proteins
  • Receptor Activator of Nuclear Factor-kappa B
  • S100 Proteins
  • S100a8 protein, mouse
  • TICAM-1 protein, mouse
  • TLR3 protein, mouse
  • Tlr4 protein, mouse
  • Tnfrsf11a protein, mouse
  • Toll-Like Receptor 3
  • Toll-Like Receptor 4
  • Cholesterol
  • p38 Mitogen-Activated Protein Kinases
  • Cathepsins
  • CTSK protein, human
  • Cathepsin K
  • Ctsk protein, mouse
  • Matrix Metalloproteinase 8
  • Matrix Metalloproteinase 14
  • rab GTP-Binding Proteins