Key Laboratory of Molecular and Cellular Biology of Ministry of Education, Hebei Province Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, College of Life Sciences, Hebei Normal University, Shijiazhuang, Hebei 050024, China; State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, University of Chinese Academy of Sciences, Beijing, China.
Key Laboratory of Molecular and Cellular Biology of Ministry of Education, Hebei Province Key Laboratory of Animal Physiology, Biochemistry and Molecular Biology, College of Life Sciences, Hebei Normal University, Shijiazhuang, Hebei 050024, China.
Ageing Res Rev. 2022 Nov;81:101702. doi: 10.1016/j.arr.2022.101702. Epub 2022 Jul 28.
Mitochondria, which serve as the energy factories of cells, are involved in cell differentiation, calcium homeostasis, amino acid and fatty acid metabolism and apoptosis. In response to environmental stresses, mitochondrial homeostasis is regulated at both the organelle and molecular levels to effectively maintain the number and function of mitochondria. The mitochondrial unfolded protein response (UPR) is an adaptive intracellular stress mechanism that responds to stress signals by promoting the transcription of genes encoding mitochondrial chaperones and proteases. The mechanism of the UPR in Caenorhabditis elegans (C. elegans) has been clarified over time, and the main regulatory factors include ATFS-1, UBL-5 and DVE-1. In mammals, the activation of the UPR involves eIF2α phosphorylation and the uORF-regulated expression of CHOP, ATF4 and ATF5. Several additional factors, such as SIRT3 and HSF1, are also involved in regulating the UPR. A deep and comprehensive exploration of the UPR can provide new directions and strategies for the treatment of human diseases, including aging, neurodegenerative diseases, cardiovascular diseases and diabetes. In this review, we mainly discuss the function of UPR, describe the regulatory mechanisms of UPR in C. elegans and mammals, and summarize the relationship between UPR and various human diseases.
线粒体是细胞的能量工厂,参与细胞分化、钙稳态、氨基酸和脂肪酸代谢以及细胞凋亡。为了应对环境压力,线粒体的稳态在细胞器和分子水平上都受到调节,以有效地维持线粒体的数量和功能。线粒体未折叠蛋白反应(UPR)是一种适应性的细胞内应激机制,通过促进编码线粒体伴侣和蛋白酶的基因的转录来响应应激信号。随着时间的推移,秀丽隐杆线虫(C. elegans)中线粒体 UPR 的机制已经得到阐明,主要的调节因子包括 ATFS-1、UBL-5 和 DVE-1。在哺乳动物中,UPR 的激活涉及 eIF2α 磷酸化和 uORF 调节的 CHOP、ATF4 和 ATF5 的表达。一些其他的因素,如 SIRT3 和 HSF1,也参与调节 UPR。深入全面地研究 UPR 可以为人类疾病的治疗提供新的方向和策略,包括衰老、神经退行性疾病、心血管疾病和糖尿病。在这篇综述中,我们主要讨论了 UPR 的功能,描述了 C. elegans 和哺乳动物中 UPR 的调节机制,并总结了 UPR 与各种人类疾病的关系。