粒体自噬
线粒体DNA
线粒体分裂
线粒体
线粒体融合
自噬
细胞生物学
化学
功能(生物学)
生物
生物化学
细胞凋亡
基因
作者
Bing Liu,Ting Sun,Yumeng Wang,Xiaoyu Xia,Shixian Cao,Kang‐Nan Wang,Qixin Chen,Zong‐Wan Mao
标识
DOI:10.1021/acs.analchem.4c01128
摘要
Mitochondrial DNA (mtDNA) is pivotal for mitochondrial morphology and function. Upon mtDNA damage, mitochondria undergo quality control mechanisms, including fusion, fission, and mitophagy. Real-time monitoring of mtDNA enables a deeper understanding of its effect on mitochondrial function and morphology. Controllable induction and real-time tracking of mtDNA dynamics and behavior are of paramount significance for studying mitochondrial function and morphology, facilitating a deeper understanding of mitochondria-related diseases. In this work, a fluorescent platinum complex was designed and developed that not only induces mitochondrial DNA (mtDNA) aggregation but also triggers mitochondrial autophagy (mitophagy) through the MDV pathway for damaged mtDNA clearance in living cells. Additionally, this complex allows for the real-time monitoring of these processes. This complex may serve as a valuable tool for studying mitochondrial microautophagy and holds promise for broader applications in cellular imaging and disease research.
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