MiR-155 inhibits transformation of macrophages into foam cells via regulating CEH expression

Fengxiang Zhang1, Jinsong Zhao1, Dapeng Sun1

  • 1Department of Cardiothoracic Surgery, The First Affiliated Hospital of JINZHOU Medical University, Jinzhou, 121001, China.

Insights

MicroRNA-155 (miR-155) inhibits atherosclerosis by preventing macrophage foam cell formation. It enhances cholesterol efflux by upregulating CEH, likely by downregulating Tim-3 expression.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Cardiovascular Research

Background:

  • Atherosclerosis pathogenesis involves macrophage transformation into foam cells.
  • The precise mechanisms of microRNA-155 (miR-155) in this process are not fully understood.

Purpose of the Study:

  • To elucidate the role and mechanism of miR-155 in regulating macrophage foam cell formation.
  • To investigate the relationship between miR-155, CEH, and Tim-3 in macrophages.

Main Methods:

  • Transfection of THP-1 macrophages with miR-155 mimics and siCEH.
  • Quantitative analysis of mRNA and protein expression levels.
  • Assessment of intracellular cholesterol accumulation and efflux.

Main Results:

  • miR-155 mimics upregulated CEH mRNA and protein expression in a dose- and time-dependent manner.
  • Overexpression of miR-155 inhibited foam cell formation, reduced CE accumulation, and enhanced cholesterol efflux.
  • siCEH reversed the effects of miR-155, and Tim-3 was found to attenuate miR-155-mediated CEH induction.

Conclusions:

  • miR-155 inhibits macrophage transformation into foam cells by enhancing the CEH signaling pathway.
  • This effect is mediated by the inhibition of Tim-3 expression, providing a novel therapeutic target for atherosclerosis.

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