扫描电镜
粒体自噬
线粒体
细胞生物学
细胞器
共焦
生物物理学
生物
显微镜
共焦显微镜
线粒体DNA
细胞内
自噬
生物化学
激光器
光学
物理
受激发射
基因
细胞凋亡
作者
Dan Zhang,Ying He,Jinying Wang,Liuying Wu,Bing Liu,Songtao Cai,Yuan Li,Wei Yan,Zhigang Yang,Junle Qu
标识
DOI:10.1002/jbio.202200006
摘要
Mitochondrion is one of significant organelles inside cells because it serves as a hub for energy management and intracellular signaling. Internal/external damages on mitochondria would lead to mitochondrial stresses with the malfunctions, accompanying with the changes of morphological structure and abnormal local environments (pH values). Mitophagy is capable of degradation of damaged mitochondrial segments to restore its normal metabolism, dynamics, and biogenesis. The dynamic structural visualization and pH quantification can be helpful for the understanding of mitochondrial functions as well as the diagnosis of disorders linking with this process. In this work, we use confocal laser scanning microscopy, STED super-resolution nanoscopy and fluorescence lifetime imaging microscopy, in conjunction with a mitochondrial probe to image the dynamic changes in the mitochondrial morphology and microenvironmental pH values during mitophagy in live cells, in particular, the structural changes of mitochondrial cristae beyond optical diffraction can be distinguished by STED nanoscopy with/without treatment by CCCP, which will provide a new view for the diagnosis and personalized treatment of mitochondrial dysfunction-related diseases.
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