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平滑肌细胞-蛋白聚糖-脂蛋白相互作用作为动脉粥样硬化的驱动因素。

Smooth Muscle Cell-Proteoglycan-Lipoprotein Interactions as Drivers of Atherosclerosis.

机构信息

Department of Medicine, Centre for Heart Lung Innovation, Providence Healthcare Research Institute, St. Paul's Hospital, University of British Columbia, Vancouver, BC, Canada.

出版信息

Handb Exp Pharmacol. 2022;270:335-358. doi: 10.1007/164_2020_364.

Abstract

In humans, smooth muscle cells (SMCs) are the main cell type in the artery medial layer, in pre-atherosclerotic diffuse thickening of the intima, and in all stages of atherosclerotic lesion development. SMCs secrete the proteoglycans responsible for the initial binding and retention of atherogenic lipoproteins in the artery intima, with this retention driving foam cell formation and subsequent stages of atherosclerosis. In this chapter we review current knowledge of the extracellular matrix generated by SMCs in medial and intimal arterial layers, their relationship to atherosclerotic lesion development and stabilization, how these findings correlate with mouse models of atherosclerosis, and potential therapies aimed at targeting the SMC matrix-lipoprotein interaction for atherosclerosis prevention.

摘要

在人类中,平滑肌细胞(SMCs)是动脉中层的主要细胞类型,存在于动脉内膜的粥样前期弥漫性增厚,以及动脉粥样硬化病变发展的所有阶段。SMC 分泌蛋白聚糖,负责初始结合和保留动脉内膜中的致动脉粥样硬化脂蛋白,这种保留驱动泡沫细胞形成和随后的动脉粥样硬化阶段。在本章中,我们回顾了 SMC 在动脉中层和内膜层中产生的细胞外基质的最新知识,它们与动脉粥样硬化病变发展和稳定的关系,这些发现与动脉粥样硬化的小鼠模型的相关性,以及针对 SMC 基质-脂蛋白相互作用的潜在治疗方法,以预防动脉粥样硬化。

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