| Literature DB >> 29702036 |
Katherine J Perschbacher1, Guorui Deng1, Rory A Fisher1, Katherine N Gibson-Corley2,3, Mark K Santillan4,3,5, Justin L Grobe1,3,5,6,7,8.
Abstract
G protein-coupled receptor signaling mechanisms are implicated in many aspects of cardiovascular control, and dysfunction of such signaling mechanisms is commonly associated with disease states. Investigators have identified a large number of regulator of G protein signaling (RGS) proteins that variously contribute to the modulation of intracellular second-messenger signaling kinetics. These many RGS proteins each interact with a specific set of second-messenger cascades and receptor types and exhibit tissue-specific expression patterns. Increasing evidence supports the contribution of RGS proteins, or their loss, in the pathogenesis of cardiovascular dysfunctions. This review summarizes the current understanding of the functional contributions of RGS proteins, particularly within the B/R4 family, in cardiovascular disorders of pregnancy including gestational hypertension, uterine artery dysfunction, and preeclampsia.Entities:
Keywords: B/R4 family; RGS2; RGS5; pregnancy; regulator of G protein signaling
Mesh:
Substances:
Year: 2018 PMID: 29702036 PMCID: PMC6139632 DOI: 10.1152/physiolgenomics.00037.2018
Source DB: PubMed Journal: Physiol Genomics ISSN: 1094-8341 Impact factor: 3.107