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Cell Death Differ ; 22(3): 419-32, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25215947

ABSTRACT

Damaged mitochondria are eliminated by mitophagy, a selective form of autophagy whose dysfunction associates with neurodegenerative diseases. PINK1, PARKIN and p62/SQTMS1 have been shown to regulate mitophagy, leaving hitherto ill-defined the contribution by key players in 'general' autophagy. In basal conditions, a pool of AMBRA1 - an upstream autophagy regulator and a PARKIN interactor - is present at the mitochondria, where its pro-autophagic activity is inhibited by Bcl-2. Here we show that, upon mitophagy induction, AMBRA1 binds the autophagosome adapter LC3 through a LIR (LC3 interacting region) motif, this interaction being crucial for regulating both canonical PARKIN-dependent and -independent mitochondrial clearance. Moreover, forcing AMBRA1 localization to the outer mitochondrial membrane unleashes a massive PARKIN- and p62-independent but LC3-dependent mitophagy. These results highlight a novel role for AMBRA1 as a powerful mitophagy regulator, through both canonical or noncanonical pathways.


Subject(s)
Adaptor Proteins, Signal Transducing/metabolism , Autophagy/physiology , Microtubule-Associated Proteins/metabolism , Mitochondria/metabolism , Neurodegenerative Diseases/metabolism , Ubiquitin-Protein Ligases/metabolism , Animals , HEK293 Cells , HeLa Cells , Heat-Shock Proteins/metabolism , Humans , Mice , Mice, Transgenic , Sequestosome-1 Protein , Transfection
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