Literature DB >> 25690012

A molecular signature in the pannexin1 intracellular loop confers channel activation by the α1 adrenoreceptor in smooth muscle cells.

Marie Billaud1, Yu-Hsin Chiu2, Alexander W Lohman1, Thibaud Parpaite3, Joshua T Butcher3, Stephanie M Mutchler3, Leon J DeLalio1, Mykhaylo V Artamonov4, Joanna K Sandilos2, Angela K Best3, Avril V Somlyo1, Roger J Thompson5, Thu H Le6, Kodi S Ravichandran7, Douglas A Bayliss2, Brant E Isakson8.   

Abstract

Both purinergic signaling through nucleotides such as ATP (adenosine 5'-triphosphate) and noradrenergic signaling through molecules such as norepinephrine regulate vascular tone and blood pressure. Pannexin1 (Panx1), which forms large-pore, ATP-releasing channels, is present in vascular smooth muscle cells in peripheral blood vessels and participates in noradrenergic responses. Using pharmacological approaches and mice conditionally lacking Panx1 in smooth muscle cells, we found that Panx1 contributed to vasoconstriction mediated by the α1 adrenoreceptor (α1AR), whereas vasoconstriction in response to serotonin or endothelin-1 was independent of Panx1. Analysis of the Panx1-deficient mice showed that Panx1 contributed to blood pressure regulation especially during the night cycle when sympathetic nervous activity is highest. Using mimetic peptides and site-directed mutagenesis, we identified a specific amino acid sequence in the Panx1 intracellular loop that is essential for activation by α1AR signaling. Collectively, these data describe a specific link between noradrenergic and purinergic signaling in blood pressure homeostasis.
Copyright © 2015, American Association for the Advancement of Science.

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Year:  2015        PMID: 25690012      PMCID: PMC4358815          DOI: 10.1126/scisignal.2005824

Source DB:  PubMed          Journal:  Sci Signal        ISSN: 1945-0877            Impact factor:   8.192


  74 in total

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