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Nectin

Authors :
Kaho Matsubara
Akira Mizoguchi
Kazushi Kimura
Tomoyuki Honda
Yoshimoto Kiyohara
Tomonari Tsutsumi
Hiroyuki Nakanishi
Kyun Heo
Chizuka Ide
Kumi Ozaki-Kuroda
Yoshimi Takai
Satomi Sonoda
Mikito Higashi
Tatsuo Katata
Source :
Journal of Cell Biology. 156:555-565
Publication Year :
2002
Publisher :
Rockefeller University Press, 2002.

Abstract

The nectin–afadin system is a novel cell–cell adhesion system that organizes adherens junctions cooperatively with the cadherin–catenin system in epithelial cells. Nectin is an immunoglobulin-like adhesion molecule, and afadin is an actin filament–binding protein that connects nectin to the actin cytoskeleton. Nectin has four isoforms (-1, -2, -3, and -4). Each nectin forms a homo-cis-dimer followed by formation of a homo-trans-dimer, but nectin-3 furthermore forms a hetero-trans-dimer with nectin-1 or -2, and the formation of each hetero-trans-dimer is stronger than that of each homo-trans-dimer. We show here that at the synapses between the mossy fiber terminals and dendrites of pyramidal cells in the CA3 area of adult mouse hippocampus, the nectin–afadin system colocalizes with the cadherin–catenin system, and nectin-1 and -3 asymmetrically localize at the pre- and postsynaptic sides of puncta adherentia junctions, respectively. During development, nectin-1 and -3 asymmetrically localize not only at puncta adherentia junctions but also at synaptic junctions. Inhibition of the nectin-based adhesion by an inhibitor of nectin-1 in cultured rat hippocampal neurons results in a decrease in synapse size and a concomitant increase in synapse number. These results indicate an important role of the nectin–afadin system in the formation of synapses.

Details

ISSN :
15408140 and 00219525
Volume :
156
Database :
OpenAIRE
Journal :
Journal of Cell Biology
Accession number :
edsair.doi.dedup.....a5abe4a81c826c5abd678b51a608e1b2
Full Text :
https://doi.org/10.1083/jcb.200103113