Reduction of Intracellular Chloride Concentration Promotes Foam Cell Formation

Circ J. 2016;80(4):1024-33. doi: 10.1253/circj.CJ-15-1209. Epub 2016 Feb 25.

Abstract

Background: Previous work has demonstrated that the volume-regulated chloride channel is activated during foam cell formation, and inhibition of chloride movement prevents intracellular lipid accumulation. However, the mechanism explaining how chloride movement promotes foam cell formation is not clear.

Methods and results: Foam cell formation was determined by Oil Red O staining. Western blotting and co-immunoprecipitation were used to examine protein expression and protein-protein interaction. [Cl(-)]iwas measured using 6-methoxy-N-ethylquinolinium iodide dye. The results showed that [Cl(-)]iwas decreased in monocytes/macrophages from patients with hypercholesterolemia and from apoE(-/-)mice fed with a high-fat diet. Lowering [Cl(-)]iupregulated scavenger receptor A (SR-A) expression, increased the binding and uptake of oxLDL, enhanced pro-inflammatory cytokine production and subsequently accelerated foam cell formation in macrophages from humans and mice. In addition, low Cl(-)solution stimulated the activation of JNK and p38 mitogen-activated protein kinases. Inhibition of JNK and p38 blocked Cl(-)reduced medium-induced SR-A expression and lipid accumulation. In contrast, reduction of [Cl(-)]ipromoted the interaction of SR-A with caveolin-1, thus facilitating caveolin-1-dependent SR-A endocytosis. Moreover, disruption of caveolae attenuated SR-A internalization, JNK and p38 activation, and ultimately prevented SR-A expression and foam cell formation stimulated by low Cl(-)medium.

Conclusions: This data provide strong evidence that reduction of [Cl(-)]iis a critical contributor to intracellular lipid accumulation, suggesting that modulation of [Cl(-)]iis a novel avenue to prevent foam cell formation and atherosclerosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apolipoproteins E / deficiency
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism
  • Chlorides / metabolism*
  • Dietary Fats / adverse effects
  • Dietary Fats / pharmacology
  • Enzyme Activation / drug effects
  • Enzyme Activation / genetics
  • Foam Cells / metabolism*
  • Foam Cells / pathology
  • Hypercholesterolemia / chemically induced
  • Hypercholesterolemia / genetics
  • Hypercholesterolemia / metabolism*
  • Hypercholesterolemia / pathology
  • MAP Kinase Kinase 4 / genetics
  • MAP Kinase Kinase 4 / metabolism
  • Mice
  • Mice, Knockout
  • Scavenger Receptors, Class A / genetics
  • Scavenger Receptors, Class A / metabolism
  • Up-Regulation / drug effects
  • p38 Mitogen-Activated Protein Kinases / genetics
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Apolipoproteins E
  • Caveolin 1
  • Chlorides
  • Dietary Fats
  • Scavenger Receptors, Class A
  • p38 Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 4