蛋白质稳态
线粒体
未折叠蛋白反应
生物
DNAJA3公司
线粒体融合
粒线体疾病
热休克蛋白60
综合应力响应
计算生物学
细胞生物学
线粒体DNA
生物信息学
热休克蛋白
遗传学
基因
翻译(生物学)
内质网
热休克蛋白70
信使核糖核酸
作者
Hedong Lu,Xiaolei Wang,Min Li,Dongmei Ji,Dan Liang,Chunmei Liang,Yajing Liu,Zhiguo Zhang,Yunxia Cao,Weiwei Zou
出处
期刊:Cells
[Multidisciplinary Digital Publishing Institute]
日期:2022-12-21
卷期号:12 (1): 20-20
被引量:16
标识
DOI:10.3390/cells12010020
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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