期刊
JOURNAL OF NEUROSCIENCE
卷 32, 期 9, 页码 2915-2930出版社
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2765-11.2012
关键词
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资金
- Deutsche Forschungsgemeinschaft [PO732, SFB621/C12]
- Center of Molecular Physiology of the Brain
- Wellcome Trust
- MRC UK
- Medical Research Council [G0900613, G0802216] Funding Source: researchfish
- MRC [G0802216, G0900613] Funding Source: UKRI
The common neurotransmitter serotonin controls different aspects of early neuronal differentiation, although the underlying mechanisms are poorly understood. Here we report that activation of the serotonin 5-HT7 receptor promotes synaptogenesis and enhances synaptic activity in hippocampal neurons at early postnatal stages. An analysis of G alpha(12)-deficient mice reveals a critical role of G(12)-protein for 5-HT7 receptor-mediated effects in neurons. In organotypic preparations from the hippocampus of juvenile mice, stimulation of 5-HT7R/G(12) signaling potentiates formation of dendritic spines, increases neuronal excitability, and modulates synaptic plasticity. In contrast, in older neuronal preparations, morphogenetic and synaptogenic effects of 5-HT7/G(12) signaling are abolished. Moreover, inhibition of 5-HT7 receptor had no effect on synaptic plasticity in hippocampus of adult animals. Expression analysis reveals that the production of 5-HT7 and G alpha(12)-proteins in the hippocampus undergoes strong regulation with a pronounced transient increase during early postnatal stages. Thus, regulated expression of 5-HT7 receptor and G alpha(12)-protein may represent a molecular mechanism by which serotonin specifically modulates formation of initial neuronal networks during early postnatal development.
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