炎症
发病机制
表型
平滑肌
表型转换
生物
细胞
谱系(遗传)
细胞生物学
心肌细胞
免疫学
生物信息学
血管平滑肌
电池类型
医学
药物治疗
细胞谱系
不利影响
临床表型
细胞生长
机制(生物学)
神经科学
癌症研究
作者
Vlad Serbulea,James Martin,Gary K. Owens
标识
DOI:10.1146/annurev-physiol-052824-084232
摘要
Major adverse cardiovascular events resulting from atherosclerotic plaque instability account for a plurality of deaths worldwide despite the use of highly effective lipid-lowering therapies. Over the last three decades, the role of inflammation in atherogenesis has been tested extensively. Although preclinical studies demonstrate a clear role for inflammation in atherogenesis, clinical studies using global anti-inflammatory therapies have not been as successful as hoped, encouraging the search for new therapeutic strategies. Thanks to the advent of cell-specific lineage tracing, we have begun to appreciate the multifaceted role of smooth muscle cell phenotypic switching in modulating plaque stability. Here, we review the mechanisms controlling smooth muscle cell phenotypic switching during early and late-stage pathogenesis, which may inspire future therapies to stabilize plaques.
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