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Publication : Opposing effects of α2- and β-adrenergic receptor stimulation on quiescent neural precursor cell activity and adult hippocampal neurogenesis.

First Author  Jhaveri DJ Year  2014
Journal  PLoS One Volume  9
Issue  6 Pages  e98736
PubMed ID  24922313 Mgi Jnum  J:217322
Mgi Id  MGI:5613753 Doi  10.1371/journal.pone.0098736
Citation  Jhaveri DJ, et al. (2014) Opposing effects of alpha2- and beta-adrenergic receptor stimulation on quiescent neural precursor cell activity and adult hippocampal neurogenesis. PLoS One 9(6):e98736
abstractText  Norepinephrine regulates latent neural stem cell activity and adult hippocampal neurogenesis, and has an important role in modulating hippocampal functions such as learning, memory and mood. Adult hippocampal neurogenesis is a multi-stage process, spanning from the activation and proliferation of hippocampal stem cells, to their differentiation into neurons. However, the stage-specific effects of noradrenergic receptors in regulating adult hippocampal neurogenesis remain poorly understood. In this study, we used transgenic Nestin-GFP mice and neurosphere assays to show that modulation of alpha2- and beta-adrenergic receptor activity directly affects Nestin-GFP/GFAP-positive precursor cell population albeit in an opposing fashion. While selective stimulation of alpha2-adrenergic receptors decreases precursor cell activation, proliferation and immature neuron number, stimulation of beta-adrenergic receptors activates the quiescent precursor pool and enhances their proliferation in the adult hippocampus. Furthermore, our data indicate no major role for alpha1-adrenergic receptors, as we did not observe any change in either the activation and proliferation of hippocampal precursors following selective stimulation or blockade of alpha1-adrenergic receptors. Taken together, our data suggest that under physiological as well as under conditions that lead to enhanced norepinephrine release, the balance between alpha2- and beta-adrenergic receptor activity regulates precursor cell activity and hippocampal neurogenesis.
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