Literature DB >> 22378867

5-HT7R/G12 signaling regulates neuronal morphology and function in an age-dependent manner.

Fritz Kobe1, Daria Guseva, Thomas P Jensen, Alexander Wirth, Ute Renner, Dietmar Hess, Michael Müller, Lucian Medrihan, Weiqi Zhang, Mingyue Zhang, Katharina Braun, Sören Westerholz, Andreas Herzog, Konstantin Radyushkin, Ahmed El-Kordi, Hannelore Ehrenreich, Diethelm W Richter, Dmitri A Rusakov, Evgeni Ponimaskin.   

Abstract

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-HT(7) receptor promotes synaptogenesis and enhances synaptic activity in hippocampal neurons at early postnatal stages. An analysis of Gα(12)-deficient mice reveals a critical role of G(12)-protein for 5-HT(7) receptor-mediated effects in neurons. In organotypic preparations from the hippocampus of juvenile mice, stimulation of 5-HT(7)R/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-HT(7)/G(12) signaling are abolished. Moreover, inhibition of 5-HT(7) receptor had no effect on synaptic plasticity in hippocampus of adult animals. Expression analysis reveals that the production of 5-HT(7) and Gα(12)-proteins in the hippocampus undergoes strong regulation with a pronounced transient increase during early postnatal stages. Thus, regulated expression of 5-HT(7) receptor and Gα(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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Year:  2012        PMID: 22378867      PMCID: PMC3369253          DOI: 10.1523/JNEUROSCI.2765-11.2012

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


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