| Literature DB >> 26773211 |
Joseph B Black1, Richard T Premont2, Yehia Daaka3.
Abstract
GPCRs are ubiquitous in mammalian cells and present intricate mechanisms for cellular signaling and communication. Mechanistically, GPCR signaling was identified to occur vectorially through heterotrimeric G proteins that are negatively regulated by GRK and arrestin effectors. Emerging evidence highlights additional roles for GRK and Arrestin partners, and establishes the existence of interconnected feedback pathways that collectively define GPCR signaling. GPCRs influence cellular dynamics and can mediate pathologic development, such as cancer and cardiovascular remolding. Hence, a better understanding of their overall signal regulation is of great translational interest and research continues to exploit the pharmacologic potential for modulating their activity.Entities:
Keywords: Arrestin; Biased signaling; G protein; GPCR; GRK; Signal transduction
Mesh:
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Year: 2016 PMID: 26773211 PMCID: PMC4779377 DOI: 10.1016/j.semcdb.2015.12.015
Source DB: PubMed Journal: Semin Cell Dev Biol ISSN: 1084-9521 Impact factor: 7.727