Proteotoxic stress response in atherosclerotic cardiovascular disease: Emerging role of heat shock factor 1

被引:3
|
作者
Ghai, Shruti [1 ]
Young, Alex [1 ]
Su, Kuo-Hui [1 ]
机构
[1] Univ Toledo, Coll Med & Life Sci, Dept Cell & Canc Biol, Toledo, OH 43606 USA
来源
关键词
heat shock proteins; heat shock factor 1; foam cells; atherosclerosis; lipid metabolism; SMOOTH-MUSCLE-CELLS; TRANSCRIPTION FACTOR-1; MOLECULAR CHAPERONES; HSF1; PROTEINS; EXPRESSION; RECEPTOR; DOMAIN; ATHEROGENESIS; INFLAMMATION;
D O I
10.3389/fcvm.2023.1155444
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atherosclerosis is a major risk factor for cardiovascular diseases. Hypercholesterolemia has been both clinically and experimentally linked to cardiovascular disease and is involved in the initiation of atherosclerosis. Heat shock factor 1 (HSF1) is involved in the control of atherosclerosis. HSF1 is a critical transcriptional factor of the proteotoxic stress response that regulates the production of heat shock proteins (HSPs) and other important activities such as lipid metabolism. Recently, HSF1 is reported to directly interact with and inhibit AMP-activated protein kinase (AMPK) to promote lipogenesis and cholesterol synthesis. This review highlights roles of HSF1 and HSPs in critical metabolic pathways of atherosclerosis, including lipogenesis and proteome homeostasis.
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页数:8
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