4.4 Review

Exciting and not so exciting roles of pannexins

Journal

NEUROSCIENCE LETTERS
Volume 695, Issue -, Pages 25-31

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2017.03.010

Keywords

Gap junctions; Seizures; Purinergic signaling; P2X receptors; Panx1; Epilepsy

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Funding

  1. National Institute of Neurological Disorders and Stroke (NINDS) of the National Institutes of Health [RO1-NS092786]

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It is the current view that purinergic signaling regulates many physiological functions. Pannexin1 (Panx1), a member of the gap junction family of proteins is an ATP releasing channel that plays important physiopathological roles in various tissues, including the CNS. Upon binding to purinergic receptors expressed in neural cells, ATP triggers cellular responses including increased cell proliferation, cell morphology changes, release of cytokines, and regulation of neuronal excitability via release of glutamate, GABA and ATP itself. Under pathological conditions such as ischemia, trauma, inflammation, and epilepsy, extracellular ATP concentrations increases drastically but the consequences of this surge is still difficult to characterize due to its rapid metabolism in ADP and adenosine, the latter having inhibitory action on neuronal activity. For seizures, for instance, the excitatory effect of ATP on neuronal activity is mainly related to its action of P2X receptors, while the inhibitory effects are related to activation of P1, adenosine receptors. Here we provide a mini review on the properties of pannexins with a main focus on Panxl and its involvement in seizure activity. Although there are only few studies implicating Panx1 in seizures, they are illustrative of the dual role that Panxl has on neuronal excitability. (C) 2017 Elsevier B.V. All rights reserved.

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