粒体自噬
自噬
生物
线粒体
细胞生物学
细胞凋亡
遗传学
作者
Katharina C. Lorentzen,Alan R. Prescott,Ian G. Ganley
标识
DOI:10.1080/15548627.2024.2395149
摘要
Macroautophagy/autophagy enables lysosomal degradation of a diverse array of intracellular material. This process is essential for normal cellular function and its dysregulation is implicated in many diseases. Given this, there is much interest in understanding autophagic mechanisms of action in order to determine how it can be best targeted therapeutically. In mitophagy, the selective degradation of mitochondria via autophagy, mitochondria first need to be primed with signals that allow the recruitment of the core autophagy machinery to drive the local formation of an autophagosome around the target mitochondrion. To determine how the recruitment of different core autophagy components can drive mitophagy, we took advantage of the
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