粒体自噬
化学
荧光
线粒体
动力学(音乐)
细胞生物学
生物物理学
自噬
细胞器
生物化学
细胞凋亡
光学
物理
声学
生物
作者
Weikang Peng,Mei Li,Wenwen Li,Yuanjuan Wang,Cheng Tian,Zhilong Zhao,Min Gao,Lei Yang
标识
DOI:10.1021/acs.analchem.5c03247
摘要
Mitophagy is a vital lysosome-dependent process in which damaged mitochondria exhibiting elevated H2O2 production are selectively engulfed by autophagosomes and delivered to lysosomes for degradation, thereby maintaining intracellular homeostasis. Consequently, monitoring mitophagy holds significant potential for disease diagnosis and therapeutic development. In this study, H2O2-activated lysosome-targeted fluorescent probe, PLM, was developed for the super-resolution imaging of the mitophagic process. The initiation of mitophagy induces the significant production of autophagosomes. Red-stained mitochondria are engulfed by blue-stained autophagosomes and subsequently fuse with lysosomes, leading to an increase in the H2O2 concentration within the lysosomes. This activates the green fluorescence signal of PLM. The entire mitophagic process can be visualized and monitored by observing changes in the fluorescence intensity of the autophagosomes and lysosomes as well as the overlap of fluorescence signals. Super-resolution imaging enables the triple-signal nanoscale visualization of the dynamic processes in three organelles. This probe was successfully applied to monitor rapamycin- and starvation-induced mitophagy and was further utilized to assess the role of mitophagy inhibition in enhancing antitumor activity.
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