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Localization of l‐afadin at puncta adhaerentia‐like junctions between the mossy fiber terminals and the dendritic trunks of pyramidal cells in the adult mouse hippocampus
Author(s) -
Nishioka Hideo,
Mizoguchi Akira,
Nakanishi Hiroyuki,
Mandai Kenji,
Takahashi Kenichi,
Kimura Kazushi,
SatohMoriya Ayako,
Takai Yoshimi
Publication year - 2000
Publication title -
journal of comparative neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.855
H-Index - 209
eISSN - 1096-9861
pISSN - 0021-9967
DOI - 10.1002/1096-9861(20000821)424:2<297::aid-cne8>3.0.co;2-j
Subject(s) - nectin , adherens junction , microbiology and biotechnology , mossy fiber (hippocampus) , immunoelectron microscopy , chemistry , hippocampal formation , biology , cadherin , adhesion , neuroscience , cell adhesion , antibody , cell , dentate gyrus , immunology , biochemistry , organic chemistry
Abstract We have recently found a novel cell–cell adhesion system at cadherin‐based adherens junctions. This system consists of at least two components: nectin, an immunoglobulin‐like cell adhesion molecule with Ca 2+ ‐independent homophilic binding activity, and l‐afadin, an actin filament‐binding protein that connects nectin to the actin cytoskeleton. In the present study, we investigated immunocytochemically the localization of l‐afadin in the mouse hippocampus. At the light microscopic level, l‐afadin immunoreactivity was demonstrated as flattened disks in the stratum lucidum of the CA3 area. By immunoelectron microscopy, signals for l‐afadin were highly concentrated in a symmetrical manner at the puncta adhaerentia‐like junctions between the mossy fiber terminals and the dendritic trunks of pyramidal cells. We furthermore immunostained the hippocampus with antibodies recognizing both l‐afadin and s‐afadin, a small splicing variant of l‐afadin that is identical to AF‐6. Immunoreactivity for l‐ and s‐afadins was demonstrated not only as the flattened disks similar to that for l‐afadin, but also as numerous fine dots widely distributed in all synaptic layers of the CA1 and CA3 areas. The latter finding may correspond with the recent report by Buchert et al. (1999, J. Cell. Biol. 144:361–371), who found that s‐afadin (AF‐6) and/or l‐afadin was localized at the postsynaptic membranes of asymmetric synaptic junctions. Our present results indicate that l‐ and s‐afadins are differentially distributed in the hippocampus and suggest that l‐afadin localized at the puncta adhaerentia‐like junctions in the mossy fiber terminals may regulate the structural and functional organization of these complex synaptic structures. J. Comp. Neurol. 424:297–306, 2000. © 2000 Wiley‐Liss, Inc.