Department of Cardiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Avenue, Wuhan 430030, PR China.
Department of Cardiology, China Three Gorges University, Yichang 433000, PR China.
Biochem Biophys Res Commun. 2014 Jul 18;450(1):500-6. doi: 10.1016/j.bbrc.2014.06.005. Epub 2014 Jun 10.
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.
线粒体融合蛋白 2(Mfn2)可抑制动脉粥样硬化斑块的形成,但其中的作用机制尚不清楚。本研究旨在揭示 Mfn2 在动脉粥样硬化中的作用。与健康对照组相比,我们发现 Mfn2 在小鼠和人类的动脉粥样硬化病变中表达显著降低。在这里,我们观察到 Mfn2 通过上调过氧化物酶体增殖物激活受体-γ(PPAR-γ)增加巨噬细胞中胆固醇转运蛋白的表达,这一作用至少部分是通过抑制细胞外信号调节激酶 1/2(ERK1/2)和 p38 丝裂原活化蛋白激酶(MAPKs)通路实现的。这些发现为 Mfn2 介导的胆固醇转运蛋白表达改变的潜在机制提供了新的认识,这可能对动脉粥样硬化性心脏病的治疗具有重要意义。