Plasticity of 5-HT1A receptor-mediated signaling during early postnatal brain development

被引:24
作者
Mehta, Mukti
Ahmed, Zagloul
Fernando, Suraj Shawn
Cano-Sanchez, Patricia
Adayev, Tatyana
Ziemnicka, Dorota
Wieraszko, Andrzej
Banerjee, Probal
机构
[1] CUNY Coll Staten Isl, MMA Inst, New York, NY USA
[2] New York State Inst Basic Res Dev Disabil, New York, NY USA
[3] CUNY Coll Staten Isl, CSI IBR Ctr Dev Neurosci, New York, NY USA
[4] CUNY Coll Staten Isl, Dept Chem, New York, NY USA
[5] CUNY, Doctoral Program Biol, New York, NY 10021 USA
关键词
5-HT1A receptor; extracellular signal-regulated kinase; hippocampus; neonatal; neurogenesis; protein kinase C alpha;
D O I
10.1111/j.1471-4159.2007.04448.x
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
The presence of serotonin 1A receptor (5-HT1A-R) in the hippocampus, amygdala, and most regions of the frontal cortex is essential between postnatal day-5-21 (P5-21) for the expression of normal anxiety levels in adult mice. Thus, the 5-HT1A-R plays a crucial role in this time window of brain development. We show that the 5-HT1A-R-mediated stimulation of extracellular signal-regulated kinases 1 and 2 (Erk1/2) in the hippocampus undergoes a transition between P6 and P15. At P6, a protein kinase C (PKC) isozyme is required for the 5-HT1A-R -> Erk1/2 cascade, which causes increased cell division in the dentate gyrus. By contrast, at P15, PKC alpha participates downstream of Erk1/2 to augment synaptic transmission through the Schaffer Collateral pathway but does not cause increased cell division. Our data demonstrate that the 5-HT1A-R -> Erk1/2 cascade uses PKC isozymes differentially, first boosting the cell division to form new hippocampal neurons at P6 and then undergoing a plastic change in mechanism to strengthen synaptic connections in the hippocampus at P15.
引用
收藏
页码:918 / 928
页数:11
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