Real-Time Monitoring of mtDNA Aggregation and Mitophagy Induced by a Fluorescent Platinum Complex in Living Cells

被引:2
|
作者
Liu, Bing [1 ]
Sun, Ting [2 ]
Wang, Yumeng [3 ]
Xia, Xiao-Yu [1 ]
Cao, Shixian [3 ]
Wang, Kang-Nan [3 ]
Chen, Qixin [2 ]
Mao, Zong-Wan [1 ]
机构
[1] Sun Yat Sen Univ, Sch Chem, MOE Key Lab Bioinorgan & Synthet Chem, State Key Lab Oncol South China, Guangzhou 510275, Peoples R China
[2] Shandong First Med Univ & Shandong Acad Med Sci, Med Sci & Technol Innovat Ctr, Sch Pharmaceut Sci, State Key Lab Adv Drug Delivery & Release Syst, Jinan 250117, Shandong, Peoples R China
[3] Shandong Univ, State Key Lab Crystal Mat, Jinan 250100, Peoples R China
基金
美国国家科学基金会;
关键词
MITOCHONDRIAL-DNA;
D O I
10.1021/acs.analchem.4c01128
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
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.
引用
收藏
页码:13421 / 13428
页数:8
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