TY - JOUR
T1 - Arcadlin is a neural activity-regulated cadherin involved in long term potentiation
AU - Yamagata, Kanato
AU - Andreasson, Katrin I.
AU - Sugiura, Hiroko
AU - Maru, Eiichi
AU - Dominique, Muller
AU - Irie, Yasuyuki
AU - Miki, Naomasa
AU - Hayashi, Yokichi
AU - Yoshioka, Masatomo
AU - Kaneko, Kenya
AU - Kato, Hiroshi
AU - Worley, Paul F.
PY - 1999/7/2
Y1 - 1999/7/2
N2 - Neural activity results in long term changes that underlie synaptic plasticity. To examine the molecular basis of activity-dependent plasticity, we have used differential cloning techniques to identify genes that are rapidly induced in brain neurons by synaptic activity. Here, we identify a novel cadherin molecule Arcadlin (activity-regulated cadherin-like protein), arcadlin mRNA is rapidly and transiently induced in hippocampal granule cells by seizures and by N-methyl-D-aspartate-dependent synaptic activity in long term potentiation. The extracellular domain of Arcadlin is most homologous to protocadherin-8; however, the cytoplasmic region is distinct from that of any cadherin family member. Arcadlin protein is expressed at the synapses and shows a homophilic binding activity in a Ca2+-dependent manner. Furthermore, application of Arcadlin antibody reduces excitatory postsynaptic potential amplitude and blocks long term potentiation in hippocampal slices. Its close homology with cadherins, its rapid inducibility by neural activity, and its involvement in synaptic transmission suggest that Arcadlin may play an important role in activity-induced synaptic reorganization underlying long term memory.
AB - Neural activity results in long term changes that underlie synaptic plasticity. To examine the molecular basis of activity-dependent plasticity, we have used differential cloning techniques to identify genes that are rapidly induced in brain neurons by synaptic activity. Here, we identify a novel cadherin molecule Arcadlin (activity-regulated cadherin-like protein), arcadlin mRNA is rapidly and transiently induced in hippocampal granule cells by seizures and by N-methyl-D-aspartate-dependent synaptic activity in long term potentiation. The extracellular domain of Arcadlin is most homologous to protocadherin-8; however, the cytoplasmic region is distinct from that of any cadherin family member. Arcadlin protein is expressed at the synapses and shows a homophilic binding activity in a Ca2+-dependent manner. Furthermore, application of Arcadlin antibody reduces excitatory postsynaptic potential amplitude and blocks long term potentiation in hippocampal slices. Its close homology with cadherins, its rapid inducibility by neural activity, and its involvement in synaptic transmission suggest that Arcadlin may play an important role in activity-induced synaptic reorganization underlying long term memory.
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U2 - 10.1074/jbc.274.27.19473
DO - 10.1074/jbc.274.27.19473
M3 - Article
C2 - 10383464
AN - SCOPUS:0033516668
SN - 0021-9258
VL - 274
SP - 19473
EP - 19479
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 27
ER -