| Literature DB >> 29428175 |
Nadine Kabbani1, Robert A Nichols2.
Abstract
The α7 nicotinic acetylcholine receptor (nAChR) is a ligand-gated ion channel (LGIC) that plays an important role in cellular calcium signaling and contributes to several neurological diseases. Agonist binding to the α7 nAChR induces fast channel activation followed by inactivation and prolonged desensitization while triggering long-lasting calcium signaling. These activities foster neurotransmitter release, synaptic plasticity, and somatodendritic regulation in the brain. We discuss here the ability of α7 nAChRs to operate in ionotropic (α7i) and metabotropic (α7m) modes, leading to calcium-induced calcium release (CICR) and G protein-associated inositol trisphosphate (IP3)-induced calcium release (IICR), respectively. Metabotropic activity extends the spatial and temporal aspects of calcium signaling by the α7 channel beyond its ionotropic limits, persisting into the desensitized state. Delineation of the ionotropic and metabotropic properties of the α7 nAChR will provide definitive indicators of moment-to-moment receptor functional status that will, in turn, spearhead new drug development.Entities:
Keywords: G proteins; calcium regulation; calcium stores; nicotinic receptor; synaptic regulation
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Year: 2018 PMID: 29428175 DOI: 10.1016/j.tips.2018.01.002
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819