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- W3017119005 endingPage "899" @default.
- W3017119005 startingPage "891" @default.
- W3017119005 abstract "Abstract Mitochondria are highly vulnerable organelles based on their complex biogenesis, entailing dependence on nuclear gene expression and efficient import strategies. They are implicated in a wide spectrum of vital cellular functions, including oxidative phosphorylation, iron-sulfur cluster synthesis, regulation of calcium homeostasis, and apoptosis. Moreover, damaged mitochondria can release mitochondrial components, such as mtDNA or cardiolipin, which are sensed as danger-associated molecular patterns and trigger innate immune signaling. Thus, dysfunctional mitochondria pose a thread not only to the cellular but also to the organismal integrity. The elimination of dysfunctional and damaged mitochondria by selective autophagy, called mitophagy, is a major mechanism of mitochondrial quality control. Certain types of stress-induced mitophagy are regulated by the mitochondrial kinase PINK1 and the E3 ubiquitin ligase Parkin, which are both linked to autosomal recessive Parkinson’s disease." @default.
- W3017119005 created "2020-04-24" @default.
- W3017119005 creator A5073070783 @default.
- W3017119005 creator A5087259567 @default.
- W3017119005 date "2020-05-01" @default.
- W3017119005 modified "2023-09-23" @default.
- W3017119005 title "PINK1 and Parkin: team players in stress-induced mitophagy" @default.
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