| Literature DB >> 33201801 |
Brian Tenner1,2, Michael Getz3, Brian Ross2, Donya Ohadi4, Christopher H Bohrer1, Eric Greenwald2, Sohum Mehta2, Jie Xiao1, Padmini Rangamani3,4, Jin Zhang2,5.
Abstract
Signaling networks are spatiotemporally organized to sense diverse inputs, process information, and carry out specific cellular tasks. In β cells, Ca2+, cyclic adenosine monophosphate (cAMP), and Protein Kinase A (PKA) exist in an oscillatory circuit characterized by a high degree of feedback. Here, we describe a mode of regulation within this circuit involving a spatial dependence of the relative phase between cAMP, PKA, and Ca2+. We show that in mouse MIN6 β cells, nanodomain clustering of Ca2+-sensitive adenylyl cyclases (ACs) drives oscillations of local cAMP levels to be precisely in-phase with Ca2+ oscillations, whereas Ca2+-sensitive phosphodiesterases maintain out-of-phase oscillations outside of the nanodomain. Disruption of this precise phase relationship perturbs Ca2+ oscillations, suggesting the relative phase within an oscillatory circuit can encode specific functional information. This work unveils a novel mechanism of cAMP compartmentation utilized for localized tuning of an oscillatory circuit and has broad implications for the spatiotemporal regulation of signaling networks.Entities:
Keywords: biochemistry; cAMP; chemical biology; computational biology; mouse; pancreatic beta cell; signaling compartmentalization; systems biology
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Year: 2020 PMID: 33201801 PMCID: PMC7671691 DOI: 10.7554/eLife.55013
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140