Estrogen stimulates activity-regulated cytoskeleton associated protein (Arc) expression via the MAPK- and PI-3K-dependent pathways in SH-SY5Y cells

被引:20
作者
Chamniansawat, Siriporn [1 ]
Chongthammakun, Sukumal [1 ,2 ]
机构
[1] Mahidol Univ, Dept Anat, Fac Sci, Bangkok 10400, Thailand
[2] Mahidol Univ, Ctr Neurosci, Fac Sci, Bangkok 10400, Thailand
关键词
Activity-regulated cytoskeleton associated protein; Estrogen; Immediate-early gene; SH-SY5Y cells; Synaptic plasticity; LONG-TERM POTENTIATION; IMMEDIATE-EARLY GENE; CULTURED HIPPOCAMPAL-NEURONS; DENDRITIC SPINE DENSITY; METHYL-D-ASPARTATE; SYNAPTIC PLASTICITY; MESSENGER-RNA; NEUROTROPHIC FACTOR; PYRAMIDAL CELLS; RECEPTOR-ALPHA;
D O I
10.1016/j.neulet.2009.01.010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Activity-regulated cytoskeleton associated protein (Arc) is known to be induced by synaptic plasticity following memory consolidation. Since estrogen has been shown to play an important role in synaptogenesis, a key aspect of the synaptic plasticity, we aimed to study the effects of estrogen on Arc expression in SH-SY5Y human neuroblastoma cells. Using quantitative real-time PCR, Western blot, and confocal immunocytochemistry techniques we found that estrogen markedly increased Arc mRNA and protein expression in SH-SY5Y cells. Estrogen-activated Arc expression was mediated via mitogen-activated protein kinase (MAPK) and phosphoinositide-3 kinase (PI-3K), but not protein kinase C (PKC) and Rho-associated kinase (ROCK), and in the estrogen receptor (ER)-dependent manner. Estrogen also significantly upregulated the dendritic spine scaffolding protein, postsynaptic density-95 (PSD-95), as well as expression of the presynaptic vesicle protein, synaptophysin. Our findings demonstrate the possible mechanisms of estrogen-induced synaptic plasticity, as well as memory consolidation. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:130 / 135
页数:6
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