Research Laboratory of Translational Medicine, Hengyang Medical College, University of South China, Hengyang, Hunan 421001, People's Republic of China; Institute of Cardiovascular Disease, Key Lab for Arteriosclerology of Hunan Province, Hengyang Medical College, University of South China, Hengyang, Hunan 421001, People's Republic of China; Departments of Clinical Medicine, Hengyang Medical College, University of South China, Hengyang, Hunan 421001, People's Republic of China.
Institute of Cardiovascular Disease, Key Lab for Arteriosclerology of Hunan Province, Hengyang Medical College, University of South China, Hengyang, Hunan 421001, People's Republic of China.
Clin Chim Acta. 2021 Sep;520:8-15. doi: 10.1016/j.cca.2021.05.015. Epub 2021 May 20.
Atherosclerosis (AS), a chronic arterial disease, is characterized by endothelial dysfunction, inflammatory reactions and lipid accumulation in parallel with aberrant angiogenesis and vascular smooth muscle cell (VSMC) proliferation. Adipose tissue has been suggested to have an integral influence on metabolism and endocrine secretion, while there have been increasing concerns about the possible involvement of adipokines in cardiovascular diseases, including AS. Here, we focused on chemerin, an adipokine highly expressed in adipose tissue, with strong evidence of an association with inflammation, endothelial dysfunction, metabolic disorder, aberrant angiogenesis, VSMC proliferation and calcification. In this review, we discuss chemerin and its receptors in the pathogenesis of AS. However, the existing data assign various, even contradictory, roles to chemerin in atherosclerosis, such as inhibiting vascular calcification and impairing endothelial function. Current studies focusing on its anti- and pro-atherogenic effects have pinpointed its distinct role in specific cell types and contexts in the pathogenesis of atherosclerosis. Therefore, the gaps in current knowledge regarding the specific role played by chemerin in the etiology of AS require additional future studies. It seems reasonable to suggest that targeted chemerin therapy can be developed as an innovative approach for treating AS.
动脉粥样硬化(AS)是一种慢性动脉疾病,其特征是内皮功能障碍、炎症反应和脂质积累,同时伴有异常的血管生成和血管平滑肌细胞(VSMC)增殖。脂肪组织被认为对代谢和内分泌分泌有重要影响,而人们越来越关注脂肪因子可能参与心血管疾病,包括 AS。在这里,我们专注于 chemerin,一种在脂肪组织中高度表达的脂肪因子,有强有力的证据表明它与炎症、内皮功能障碍、代谢紊乱、异常的血管生成、VSMC 增殖和钙化有关。在这篇综述中,我们讨论了 chemerin 及其在动脉粥样硬化发病机制中的受体。然而,现有的数据赋予了 chemerin 在动脉粥样硬化中各种甚至相互矛盾的作用,例如抑制血管钙化和损害内皮功能。目前的研究集中在其抗动脉粥样硬化和促动脉粥样硬化作用上,已经确定了其在动脉粥样硬化发病机制中特定细胞类型和环境中的独特作用。因此,关于 chemerin 在动脉粥样硬化病因学中具体作用的现有知识差距需要进一步的未来研究。因此,似乎可以合理地建议,靶向 chemerin 治疗可以作为治疗 AS 的一种创新方法。