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一种分泌型磷脂酶 A 诱导平滑肌泡沫细胞形成,后者向巨噬细胞样状态转化。

A Secreted Phospholipase A Induces Formation of Smooth Muscle Foam Cells Which Transdifferentiate to Macrophage-Like State.

机构信息

Pharmacology Laboratory, Butantan Institute, 05503-900 São Paulo, Brazil.

Department of Cardiology and Angiology, Internal medicine, Otto-von-Guericke-Universität Magdeburg, 39120 Magdeburg, Germany.

出版信息

Molecules. 2019 Sep 6;24(18):3244. doi: 10.3390/molecules24183244.

Abstract

Vascular smooth muscle cells (VSMCs) loaded with lipid droplets (LDs) are markers of atherosclerosis. In this disease, inflammatory Group IIA-secreted phospholipase As (GIIA sPLAs) are highly expressed in VSMCs, but their actions in these cells are unknown. Here, we investigated the ability of myotoxin III (MT-III), an ophidian GIIA sPLA sharing structural and functional features with mammalian GIIA sPLAs, to induce LD formation and lipid metabolism factors involved in this effect. Modulation of VSMC phenotypes by this sPLA was also evaluated. Incubation of VSMCs with MT-III significantly increased the number of LDs. MT-III upregulated scavenger receptor type 1 (SR-A1) and lectin-like oxidized low-density lipoprotein receptor-1 (LOX-1) protein expression and enhanced acetylated-low density lipoprotein (acLDL) uptake by VSMCs, revealing the ability of a GIIA PLA to modulate scavenger receptor activities. MT-III induced translocation and protein expression of PPAR-γ and -β/δ. Inhibition of peroxisome proliferator-activated receptors (PPARs) and diacylglycerol O-acyltransferase (DGAT) and acyl-CoA:cholesterolacyltransferase (ACAT) enzymes abrogated MT-III-induced LD formation. Moreover, in response to MT-III, VSMCs acquired phagocytic activity and expressed macrophage markers CD68 and MAC-2. In conclusion, MT-III is able to stimulate VSMCs and recruit factors involved in lipid uptake and metabolism, leading to the formation of VSMC-derived foam cells with acquisition of macrophage-like markers and functions.

摘要

载脂滴的血管平滑肌细胞 (VSMC) 是动脉粥样硬化的标志物。在这种疾病中,炎症性 IIA 组分泌的磷脂酶 A2 (GIIA sPLA) 在 VSMC 中高度表达,但它们在这些细胞中的作用尚不清楚。在这里,我们研究了蛇毒 IIA sPLA 肌毒素 III (MT-III) 诱导 LD 形成和参与这种效应的脂质代谢因子的能力,该 sPLA 与哺乳动物 GIIA sPLA 具有结构和功能特征。还评估了这种 sPLA 对 VSMC 表型的调节作用。MT-III 孵育 VSMC 可显著增加 LD 的数量。MT-III 上调了清道夫受体 1 (SR-A1) 和凝集素样氧化型低密度脂蛋白受体 1 (LOX-1) 蛋白表达,并增强了 VSMC 对乙酰化低密度脂蛋白 (acLDL) 的摄取,揭示了 GIIA PLA 调节清道夫受体活性的能力。MT-III 诱导 PPAR-γ 和 -β/δ 的易位和蛋白表达。过氧化物酶体增殖物激活受体 (PPAR)、二酰基甘油 O-酰基转移酶 (DGAT) 和酰基辅酶 A:胆固醇酰基转移酶 (ACAT) 酶的抑制作用阻断了 MT-III 诱导的 LD 形成。此外,MT-III 使 VSMC 获得吞噬活性并表达巨噬细胞标志物 CD68 和 MAC-2。总之,MT-III 能够刺激 VSMC 并募集参与脂质摄取和代谢的因子,导致 VSMC 来源的泡沫细胞形成,并获得巨噬细胞样标志物和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4919/6766822/2e1994a04bb8/molecules-24-03244-g001.jpg

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