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Publication Detail

Title: Muscarinic receptor-activated signal transduction pathways involved in the neuritogenic effect of astrocytes in hippocampal neurons.

Authors: Guizzetti, Marina; Moore, Nadia H; VanDeMark, Kathryn L; Giordano, Gennaro; Costa, Lucio G

Published In Eur J Pharmacol, (2011 Jun 1)

Abstract: Astrocytes have been shown to release factors that affect various aspects of neuronal development. We have previously shown that the acetylcholine analog carbachol, by activating muscarinic M(3) receptors in rat astrocytes, increases their ability to promote neuritogenesis in hippocampal neurons. This effect was mediated by an increased expression and release by astrocytes of several permissive factors, a most relevant of which was fibronectin. In the present study we investigated the signal transduction pathways involved in these effects of carbachol in astrocytes. Results show that multiple pathways are involved in the effects of carbachol on astrocyte-mediated increases in fibronectin expression and neuritogenesis. These include the phospholipase D pathway, leading to sequential activation of protein kinase C (PKC) ýý, p70S6 kinase and nuclear factor-ýýB; the phosphoinositide-3 kinase pathway; and the PKC ýý pathway leading to activation of mitogen activated protein kinase. These pathways were shown to mediate the effect of carbachol on neurite outgrowth as well as the increased expression of fibronectin, further substantiating the important role of the latter in astrocyte-mediated neuritogenesis. Interference with these signaling pathways would be expected to impair astrocyte-neurons communication leading to impaired neuronal development.

PubMed ID: 21453700 Exiting the NIEHS site

MeSH Terms: Animals; Astrocytes/cytology*; Astrocytes/drug effects; Astrocytes/metabolism*; Carbachol/pharmacology; Fibronectins/metabolism; Gene Expression Regulation/drug effects; Hippocampus/cytology*; Neurites/drug effects; Neurites/metabolism*; Rats; Receptors, Muscarinic/metabolism*; Signal Transduction*/drug effects

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