Mitochondrial Unfolded Protein Response and Integrated Stress Response as Promising Therapeutic Targets for Mitochondrial Diseases

被引:10
|
作者
Lu, Hedong [1 ,2 ,3 ]
Wang, Xiaolei [1 ,2 ,3 ]
Li, Min [1 ,2 ,3 ]
Ji, Dongmei [1 ,4 ,5 ]
Liang, Dan [1 ,4 ,5 ]
Liang, Chunmei [1 ,4 ,5 ]
Liu, Yajing [1 ,4 ,5 ]
Zhang, Zhiguo [1 ,2 ,3 ]
Cao, Yunxia [1 ,2 ,3 ]
Zou, Weiwei [1 ,2 ,3 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Reprod Med Ctr, Dept Obstet & Gynecol, 218 Jixi Rd, Hefei 230022, Peoples R China
[2] Anhui Med Univ, NHC Key Lab Study Abnormal Gametes & Reprod Tract, 81 Meishan Rd, Hefei 230032, Peoples R China
[3] Anhui Med Univ, Key Lab Populat Hlth Life Cycle, Minist Educ Peoples Republ China, 81 Meishan Rd, Hefei 230032, Peoples R China
[4] Anhui Prov Key Lab Reprod Hlth & Genet, 81 Meishan Rd, Hefei 230032, Peoples R China
[5] Anhui Med Univ, Anhui Prov Engn Res Ctr, Biopreservat & Artificial Organs, 81 Meishan Rd, Hefei 230032, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
mitochondrial unfolded protein response; integrated stress response; mitochondrial diseases; mitochondrial function; MELAS SYNDROME; MESSENGER-RNA; MUTATIONS; NUCLEAR; UPR; TRANSLATION; ATF5; PROTEOSTASIS; MAINTENANCE; DEFICIENCY;
D O I
10.3390/cells12010020
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The development and application of high-throughput omics technologies have enabled a more in-depth understanding of mitochondrial biosynthesis metabolism and the pathogenesis of mitochondrial diseases. In accordance with this, a host of new treatments for mitochondrial disease are emerging. As an essential pathway in maintaining mitochondrial proteostasis, the mitochondrial unfolded protein response (UPRmt) is not only of considerable significance for mitochondrial substance metabolism but also plays a fundamental role in the development of mitochondrial diseases. Furthermore, in mammals, the integrated stress response (ISR) and UPRmt are strongly coupled, functioning together to maintain mitochondrial function. Therefore, ISR and UPRmt show great application prospects in the treatment of mitochondrial diseases. In this review, we provide an overview of the molecular mechanisms of ISR and UPRmt and focus on them as potential targets for mitochondrial disease therapy.
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页数:15
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