Two distinct mechanisms target membrane proteins to the axonal surface.

Détails

ID Serval
serval:BIB_544646FE368E
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Two distinct mechanisms target membrane proteins to the axonal surface.
Périodique
Neuron
Auteur⸱e⸱s
Sampo B., Kaech S., Kunz S., Banker G.
ISSN
0896-6273 (Print)
ISSN-L
0896-6273
Statut éditorial
Publié
Date de publication
2003
Volume
37
Numéro
4
Pages
611-624
Langue
anglais
Résumé
We have investigated the trafficking of two endogenous axonal membrane proteins, VAMP2 and NgCAM, in order to elucidate the cellular events that underlie their polarization. We found that VAMP2 is delivered to the surface of both axons and dendrites, but preferentially endocytosed from the dendritic membrane. A mutation in the cytoplasmic domain of VAMP2 that inhibits endocytosis abolished its axonal polarization. In contrast, the targeting of NgCAM depends on sequences in its ectodomain, which mediate its sorting into carriers that preferentially deliver their cargo proteins to the axonal membrane. These observations show that neurons use two distinct mechanisms to polarize proteins to the axonal domain: selective retention in the case of VAMP2, selective delivery in the case of NgCAM.
Mots-clé
Amino Acid Motifs/physiology, Animals, Axons/metabolism, Axons/ultrastructure, Cell Adhesion Molecules, Neuron-Glia/metabolism, Cell Membrane/metabolism, Cells, Cultured, Dendrites/metabolism, Dendrites/ultrastructure, Endocytosis/physiology, Membrane Proteins/metabolism, Neurons/metabolism, Neurons/ultrastructure, Protein Structure, Tertiary/physiology, Protein Transport/physiology, R-SNARE Proteins, Rats
Pubmed
Web of science
Open Access
Oui
Création de la notice
17/04/2013 12:56
Dernière modification de la notice
20/08/2019 15:09
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