首页|内质网应激与心血管疾病的研究进展

内质网应激与心血管疾病的研究进展

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内质网(ER)是真核细胞最主要的膜性结构,是细胞内重要生理过程发生的关键细胞器.在多种内外因素的作用下,ER的稳态受到破坏,导致蛋白质加工运输受阻,未折叠蛋白或错误折叠蛋白在ER腔内聚集,形成内质网应激(ERS),并触发未折叠蛋白反应(UPR).适度的ERS通过UPR信号通路减少蛋白质合成、促进蛋白质降解、增加协助蛋白质折叠的分子伴侣,最终缓解ER压力.但是,如果ERS过强或持续时间过长,超过细胞的自身调节能力时,UPR可启动细胞凋亡,亦可导致疾病.大量研究表明,ERS与多种心血管疾病(CVD)的发生发展密切相关.该综述主要阐述UPR在几种常见CVD中的研究进展和靶向UPR作为CVD的潜在治疗方法.
Research advances in endoplasmic reticulum stress and cardiovascular disease
Endoplasmic reticulum(ER)is the predominant membrane structure in eukaryotic cells and is a key or-ganelle for the occurrence of important intracellular physiological processes.Under the action of various internal and ex-ternal factors,the homeostasis of ER is disrupted to block protein processing and transport,and the accumulation of unfol-ded or misfolded proteins in the ER lumen,forms endoplasmic reticulum stress(ERS)and triggers the unfolded protein re-sponse(UPR).Moderate ERS reduces protein synthesis,promotes protein degradation,and increases molecular chaper-ones that assist protein folding through the UPR signaling pathway,ultimately relieving ER stress.However,if the ERS is too strong or prolonged and exceeds the cell's ability to regulate itself,the UPR can initiate apoptosis and lead to diseases.Numerous studies have shown that ERS is closely associated with the development of several cardiovascular diseases(CVD).This review focuses on the research progress of UPR in several common types of CVD and targets UPR as a po-tential therapeutic approach for CVD.

endoplasmic reticulum stressunfolded protein responsecardiovascular disease

李亮、张梅、陈克明

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兰州理工大学生命科学与工程学院

中国人民解放军联勤保障部队第九四○医院基础医学实验室,甘肃省兰州市 730050

内质网应激 未折叠蛋白反应 心血管疾病

中国人民解放军联勤保障部队第九四○医院实验室培育项目中国人民解放军联勤保障部队第九四○医院实验室培育项目全军动物实验专项甘肃省自然科学基金实验动物专项

2021yxky0812021yxky083SYDW201812号22JR5RA023

2024

中国动脉硬化杂志
中国病理生理学会 南华大学

中国动脉硬化杂志

CSTPCD
影响因子:1.086
ISSN:1007-3949
年,卷(期):2024.32(4)
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