Synaptic localization of growth-associated protein 43 in cultured hippocampal neurons during synaptogenesis

被引:26
作者
Morita, Shoko [1 ]
Miyata, Seiji [1 ]
机构
[1] Kyoto Inst Technol, Dept Appl Biol, Sakyo Ku, Kyoto 6068585, Japan
基金
日本学术振兴会;
关键词
synaptic plasticity; synapse; hippocampus; growth cone; orphan; GAP-43; PHOSPHORYLATION; GRANULE CELLS; ADULT-RAT; NEURITE OUTGROWTH; NERVOUS-SYSTEM; MESSENGER-RNA; IN-VIVO; EXPRESSION; CORTEX; BRAIN;
D O I
10.1002/cbf.2914
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growth-associated protein 43 (GAP-43), a novel axonal phosphoprotein, is originally identified as a growth-cone-specific protein of developing neurons in vitro. The expression of GAP-43 is also shown to be up-regulated concomitant with increased synaptic plasticity in the brains in vivo, but how GAP-43 is concerned with synaptic plasticity is not well understood. In the present study, therefore, we aimed to elucidate subcellular localization of GAP-43 as culture development of rat hippocampal neurons. Western blotting showed that the expression of GAP-43 in the cerebral and hippocampal tissues was prominently high at postnatal days 14 and 21 or the active period of synaptogenesis. Double-labelling immunohistochemistry with an axonal marker Tau revealed that the immunoreactivity of GAP-43 was seen throughout axons of cultured hippocampal neurons but stronger at axonal puncta of developing neurons than axonal processes. Double-labelling immunohistochemistry with presynaptic terminal markers of synapsin and synaptotagmin revealed that the immunoreactivity of GAP-43 was observed mostly at weak synapsin- and synaptotagmin-positive puncta rather than strong ones. The quantitative analysis of immunofluorescent intensity showed a clear inverse correlation between GAP-43 and either synapsin or synaptotagmin expression. These data indicate that GAP-43 is highly expressed at immature growing axonal terminals and its expression is decreased along with the maturation of synaptogenesis. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:400 / 411
页数:12
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