HSPB1 Regulates Autophagy and Apoptosis in Vascular Smooth Muscle Cells in Arteriosclerosis Obliterans

Objective. Small heat shock protein-1 (HSPB1) is a small heat shock protein that participates in many cellular processes and alleviates stress-induced cell injury. Autophagy protects cells from many types of stress and plays a key role in preventing stress in arteriosclerosis obliterans (ASO). Howev...

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Veröffentlicht in:Cardiovascular therapeutics 2022-11, Vol.2022, p.3889419-11
Hauptverfasser: Chen, Keqin, Hou, Changmiao, Xu, Lei, Peng, Hanwu, He, Chaogui, Liu, Jing, Wang, Guoqing, Huang, Shaoshuai, Liu, Xiehong
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Sprache:eng
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Zusammenfassung:Objective. Small heat shock protein-1 (HSPB1) is a small heat shock protein that participates in many cellular processes and alleviates stress-induced cell injury. Autophagy protects cells from many types of stress and plays a key role in preventing stress in arteriosclerosis obliterans (ASO). However, the roles of HSPB1 in autophagy and apoptosis in the context of ASO pathogenesis remain unclear. Methods. In vivo and in vitro studies were used to determine whether HSPB1 is associated with ASO progression. The expression of HSPB1 was measured in normal and sclerotic blood vessels. The role of HSPB1 and its potential downstream signaling pathway were determined in VSMCs by overexpressing and silencing HSPB1. Results. A total of 91 ASO patients admitted to and treated at our hospital from Sep. 2020 to Sep. 2021 were selected, and plasma HSPB1 expression was assessed. We divided the patients with ASO into the grade I (n=39), II (n=29), III (n=10), and IV (n=13) groups according to Fontaine’s classification. Plasma HSPB1 levels were markedly decreased in patients with grade III (n=10) and IV (n=13) ASO compared with patients with grade I ASO. Furthermore, HSPB1 expression was significantly decreased, and p62 and cleaved caspase-3 were increased in the sclerotic vasculature compared to the normal vasculature (p
ISSN:1755-5914
1755-5922
DOI:10.1155/2022/3889419