Woo Sang-Ho, Kim Dae-Yong, Choi Jae-Hoon
Department of Veterinary Pathology, College of Veterinary Medicine, Seoul National University, Seoul, Korea.
Department of Life Science, College of Natural Sciences, Research Institute of Natural Sciences, Research Institute for Convergence of Basic Sciences, Hanyang Institute of Bioscience and Biotechnology, Hanyang University, Seoul, Korea.
J Lipid Atheroscler. 2023 May;12(2):106-118. doi: 10.12997/jla.2023.12.2.106. Epub 2023 May 3.
The accumulation of calcium in atherosclerotic plaques is a prominent feature of advanced atherosclerosis, and it has a strong positive correlation with the total burden of atherosclerosis. Atherosclerotic calcification usually appears first at the necrotic core, indicating that cell death and inflammatory processes are involved in calcification. During atherosclerotic inflammation, various cell types, such as vascular smooth muscle cells, nascent resident pericytes, circulating stem cells, or adventitial cells, have been assumed to differentiate into osteoblastic cells, which lead to vascular calcification. Among these cell types, vascular smooth muscle cells are considered a major contributor to osteochondrogenic cells in the atherosclerotic milieu. In this review, we summarize the molecular mechanisms underlying the osteochondrogenic switch of vascular smooth muscle cells in atherosclerotic plaques.
钙在动脉粥样硬化斑块中的积聚是晚期动脉粥样硬化的一个显著特征,并且它与动脉粥样硬化的总负担呈强正相关。动脉粥样硬化钙化通常首先出现在坏死核心,这表明细胞死亡和炎症过程参与了钙化。在动脉粥样硬化炎症期间,各种细胞类型,如血管平滑肌细胞、新生的驻留周细胞、循环干细胞或外膜细胞,被认为会分化为成骨细胞,从而导致血管钙化。在这些细胞类型中,血管平滑肌细胞被认为是动脉粥样硬化环境中骨软骨生成细胞的主要贡献者。在这篇综述中,我们总结了动脉粥样硬化斑块中血管平滑肌细胞骨软骨生成转变的分子机制。