| Literature DB >> 24928385 |
Chun Liu1, Beihai Ge1, Chao He2, Yi Zhang1, Xiaowen Liu1, Kejian Liu3, Cuiping Qian1, Yu Zhang1, Wenzhong Peng1, Xiaomei Guo4.
Abstract
Mitofusin 2 (Mfn2) inhibits atherosclerotic plaque formation, but the underlying mechanism remains elusive. This study aims to reveal how Mfn2 functions in the atherosclerosis. Mfn2 expression was found to be significantly reduced in arterial atherosclerotic lesions of both mice and human compared with healthy counterparts. Here, we observed that Mfn2 increased cellular cholesterol transporter expression in macrophages by upregulating peroxisome proliferator-activated receptor-γ, an effect achieved at least partially by inhibiting extracellular signal-regulated kinase1/2 (ERK1/2) and p38 mitogen-activated protein kinases (MAPKs) pathway. These findings provide insights into potential mechanisms of Mfn2-mediated alterations in cholesterol transporter expression, which may have significant implications for the treatment of atherosclerotic heart disease.Entities:
Keywords: ATP binding cassette transporter A1; ATP binding cassette transporter G1; Mitofusin 2; Peroxisome proliferator-activated receptor γ; Scavenger receptor class B type I
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Year: 2014 PMID: 24928385 DOI: 10.1016/j.bbrc.2014.06.005
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575