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

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 subunits of the vacuolar ATPase (V-ATPase) proton pump...

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Veröffentlicht in:Development (Cambridge) Jg. 137; H. 11; S. 1825
Hauptverfasser: Vaccari, Thomas, Duchi, Serena, Cortese, Katia, Tacchetti, Carlo, Bilder, David
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England 01.06.2010
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ISSN:1477-9129, 1477-9129
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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 subunits of the vacuolar ATPase (V-ATPase) proton pump. Cells lacking V-ATPase function display impaired acidification of the endosomal compartment 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. V-ATPase activity is required in signal-receiving cells for Notch signaling downstream of ligand activation but upstream of gamma-secretase-dependent S3 cleavage. These data indicate that V-ATPase, probably via acidification of early endosomes, promotes not only the degradation of Notch in the lysosome but also the activation of Notch signaling in endosomes. The results also suggest that the ionic properties of the endosomal lumen might regulate Notch cleavage, providing a rationale for physiological as well as pathological endocytic control of Notch activity.
AbstractList 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 subunits of the vacuolar ATPase (V-ATPase) proton pump. Cells lacking V-ATPase function display impaired acidification of the endosomal compartment 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. V-ATPase activity is required in signal-receiving cells for Notch signaling downstream of ligand activation but upstream of gamma-secretase-dependent S3 cleavage. These data indicate that V-ATPase, probably via acidification of early endosomes, promotes not only the degradation of Notch in the lysosome but also the activation of Notch signaling in endosomes. The results also suggest that the ionic properties of the endosomal lumen might regulate Notch cleavage, providing a rationale for physiological as well as pathological endocytic control of Notch activity.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 subunits of the vacuolar ATPase (V-ATPase) proton pump. Cells lacking V-ATPase function display impaired acidification of the endosomal compartment 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. V-ATPase activity is required in signal-receiving cells for Notch signaling downstream of ligand activation but upstream of gamma-secretase-dependent S3 cleavage. These data indicate that V-ATPase, probably via acidification of early endosomes, promotes not only the degradation of Notch in the lysosome but also the activation of Notch signaling in endosomes. The results also suggest that the ionic properties of the endosomal lumen might regulate Notch cleavage, providing a rationale for physiological as well as pathological endocytic control of Notch activity.
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 subunits of the vacuolar ATPase (V-ATPase) proton pump. Cells lacking V-ATPase function display impaired acidification of the endosomal compartment 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. V-ATPase activity is required in signal-receiving cells for Notch signaling downstream of ligand activation but upstream of gamma-secretase-dependent S3 cleavage. These data indicate that V-ATPase, probably via acidification of early endosomes, promotes not only the degradation of Notch in the lysosome but also the activation of Notch signaling in endosomes. The results also suggest that the ionic properties of the endosomal lumen might regulate Notch cleavage, providing a rationale for physiological as well as pathological endocytic control of Notch activity.
Author Tacchetti, Carlo
Cortese, Katia
Bilder, David
Vaccari, Thomas
Duchi, Serena
Author_xml – sequence: 1
  givenname: Thomas
  surname: Vaccari
  fullname: Vaccari, Thomas
  email: thomas.vaccari@ifom-ieo-campus.it
  organization: Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA. thomas.vaccari@ifom-ieo-campus.it
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  givenname: Serena
  surname: Duchi
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  surname: Cortese
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  givenname: Carlo
  surname: Tacchetti
  fullname: Tacchetti, Carlo
– sequence: 5
  givenname: David
  surname: Bilder
  fullname: Bilder, David
BackLink https://www.ncbi.nlm.nih.gov/pubmed/20460366$$D View this record in MEDLINE/PubMed
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Snippet Evidence indicates that endosomal entry promotes signaling by the Notch receptor, but the mechanisms involved are not clear. In a search for factors that...
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StartPage 1825
SubjectTerms Animals
Animals, Genetically Modified
Drosophila - genetics
Drosophila - growth & development
Drosophila - metabolism
Drosophila Proteins - genetics
Drosophila Proteins - metabolism
Endosomes - metabolism
Eye - growth & development
Eye - metabolism
Eye - ultrastructure
Genes, Insect
Hydrogen-Ion Concentration
Lysosomes - metabolism
Microscopy, Electron, Transmission
Mutation
Receptors, Notch - genetics
Receptors, Notch - metabolism
Signal Transduction
Vacuolar Proton-Translocating ATPases - genetics
Vacuolar Proton-Translocating ATPases - metabolism
Title The vacuolar ATPase is required for physiological as well as pathological activation of the Notch receptor
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