生物
线粒体融合
线粒体
线粒体分裂
细胞器
超微结构
功能(生物学)
线粒体DNA
细胞生物学
基因
遗传学
解剖
作者
Rubén Quintana–Cabrera,Luca Scorrano
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2023-03-01
卷期号:83 (6): 857-876
被引量:149
标识
DOI:10.1016/j.molcel.2023.02.012
摘要
Mitochondria are not only central organelles in metabolism and energy conversion but are also platforms for cellular signaling cascades. Classically, the shape and ultrastructure of mitochondria were depicted as static. The discovery of morphological transitions during cell death and of conserved genes controlling mitochondrial fusion and fission contributed to establishing the concept that mitochondrial morphology and ultrastructure are dynamically regulated by mitochondria-shaping proteins. These finely tuned, dynamic changes in mitochondrial shape can in turn control mitochondrial function, and their alterations in human diseases suggest that this space can be explored for drug discovery. Here, we review the basic tenets and molecular mechanisms of mitochondrial morphology and ultrastructure, describing how they can coordinately define mitochondrial function.
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