Chen Yi, Li Meng, Wu Yanqing
Department of Cardiology, The Second Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Mol Med Rep. 2025 Mar;31(3). doi: 10.3892/mmr.2025.13447. Epub 2025 Jan 31.
Small heat shock proteins (sHSPs) are common molecular chaperone proteins that function in various biological processes, and serve indispensable roles in maintaining cellular protein homeostasis and regulating the hydrolysis of unfolded proteins. HSP22 is a member of the sHSP family that is primarily expressed in the heart and skeletal muscle, as well as in various types of cancer. There have been important findings concerning the role of HSP22 in cardiovascular diseases. The aim of the present study was to provide insights into the various molecular mechanisms by which HSP22 functions in the heart, including oxidative stress, autophagy, apoptosis, the subcellular distribution of proteins and the promoting effect of proteasomes. In addition, drugs and cytokines, including geranylgeranylacetone, can exert protective effects on the heart by regulating the expression of HSP22. Based on increasingly abundant research, HSP22 may be considered a potential therapeutic target in cardiovascular diseases.
小分子热休克蛋白(sHSPs)是常见的分子伴侣蛋白,在各种生物过程中发挥作用,在维持细胞蛋白质稳态和调节未折叠蛋白的水解中起着不可或缺的作用。HSP22是sHSP家族的成员,主要在心脏、骨骼肌以及各种类型的癌症中表达。关于HSP22在心血管疾病中的作用已有重要发现。本研究的目的是深入了解HSP22在心脏中发挥作用的各种分子机制,包括氧化应激、自噬、凋亡、蛋白质的亚细胞分布以及蛋白酶体的促进作用。此外,包括香叶基香叶基丙酮在内的药物和细胞因子可通过调节HSP22的表达对心脏发挥保护作用。基于越来越丰富的研究,HSP22可能被视为心血管疾病的潜在治疗靶点。