Evidence indicates that endosomal entry promotes signaling by the Notch receptor, but the mechanisms involved are not clear. In a search for factors that regulate Notch activation in endosomes, we isolated mutants in Drosophila genes that encode subunitsof the vacuolar ATPase (V-ATPase) proton pump. Cells lacking V-ATPase function display impaired acidification of the endosomalcompartment and a correlated failure to degrade endocytic cargoes. V-ATPase mutant cells internalize Notch and accumulate it in the lysosome, but surprisingly also show a substantial loss of both physiological and ectopic Notch activation in endosomes. VATPase activity is required in signal-receiving cells for Notch signaling downstream of ligand activation but upstream of -secretase-dependent S3 cleavage. These data indicate that V-ATPase, probably via acidification of early endosomes, promotes notonly the degradation of Notch in the lysosome but also the activation of Notch signaling in endosomes. The results also suggestthat the ionic properties of the endosomal lumen might regulate Notch cleavage, providing a rationale for physiological as wellas pathological endocytic control of Notch activity.

The vacuolar ATPase is required for physiological as well as pathological activation of the Notch receptor

CORTESE, KATIA;TACCHETTI, CARLO;
2010

Abstract

Evidence indicates that endosomal entry promotes signaling by the Notch receptor, but the mechanisms involved are not clear. In a search for factors that regulate Notch activation in endosomes, we isolated mutants in Drosophila genes that encode subunitsof the vacuolar ATPase (V-ATPase) proton pump. Cells lacking V-ATPase function display impaired acidification of the endosomalcompartment and a correlated failure to degrade endocytic cargoes. V-ATPase mutant cells internalize Notch and accumulate it in the lysosome, but surprisingly also show a substantial loss of both physiological and ectopic Notch activation in endosomes. VATPase activity is required in signal-receiving cells for Notch signaling downstream of ligand activation but upstream of -secretase-dependent S3 cleavage. These data indicate that V-ATPase, probably via acidification of early endosomes, promotes notonly the degradation of Notch in the lysosome but also the activation of Notch signaling in endosomes. The results also suggestthat the ionic properties of the endosomal lumen might regulate Notch cleavage, providing a rationale for physiological as wellas pathological endocytic control of Notch activity.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11567/266291
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