TY - JOUR
T1 - Nectin
T2 - An adhesion molecule involved in formation of synapses
AU - Mizoguchi, Akira
AU - Nakanishi, Hiroyuki
AU - Kimura, Kazushi
AU - Matsubara, Kaho
AU - Ozaki-Kuroda, Kumi
AU - Katata, Tatsuo
AU - Honda, Tomoyuki
AU - Kiyohara, Yoshimoto
AU - Heo, Kyun
AU - Higashi, Mikito
AU - Tsutsumi, Tomonari
AU - Sonoda, Satomi
AU - Ide, Chizuka
AU - Takai, Yoshimi
PY - 2002/2/4
Y1 - 2002/2/4
N2 - 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.
AB - 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.
KW - Afadin
KW - Cadherin
KW - Nectin
KW - Puncta adherentia junctions
KW - Synaptic junctions
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U2 - 10.1083/jcb.200103113
DO - 10.1083/jcb.200103113
M3 - Article
C2 - 11827984
AN - SCOPUS:0037017401
SN - 0021-9525
VL - 156
SP - 555
EP - 565
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 3
ER -