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G protein-coupled receptor kinase 2 (GRK2) as an integrative signalling node in the regulation of cardiovascular function and metabolic homeostasis.
- Source :
-
Cellular signalling [Cell Signal] 2018 Jan; Vol. 41, pp. 25-32. Date of Electronic Publication: 2017 Apr 04. - Publication Year :
- 2018
-
Abstract
- G protein-coupled receptor kinase 2 (GRK2) is emerging as a pivotal signalling hub able to integrate different transduction cascades. This ability appears to underlie its central role in different physiological and pathological conditions. Key mediators of cardiovascular function (such as catecholamines or angiotensin II) and components of the systemic milieu altered in insulin resistance conditions converge in increasing GRK2 levels in diverse cardiovascular cell types. In turn, GRK2 would simultaneously modulate several cardiovascular regulatory pathways, including GPCR and insulin signalling cascades, NO bioavailability and mitochondrial function. This fact can help explain the contribution of increased GRK2 levels to maladaptive cardiovascular function and remodeling. It also unveils GRK2 as a link between cardiovascular pathologies and co-morbidities such as obesity or type 2 diabetes. On the other hand, enhanced GRK2 expression, as observed in adipose tissues, liver or skeletal muscle during insulin resistance-related pathologies, could modify the orchestration of GPCR and insulin signalling in these crucial metabolic organs, and contribute to key features of the obese and insulin-resistant phenotype.<br /> (Copyright © 2017 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Animals, Genetically Modified
G-Protein-Coupled Receptor Kinase 2 genetics
Humans
Insulin metabolism
Insulin Resistance
Models, Animal
Receptors, G-Protein-Coupled genetics
Cardiovascular Diseases metabolism
Diabetes Mellitus, Type 2 metabolism
G-Protein-Coupled Receptor Kinase 2 metabolism
Obesity metabolism
Receptors, G-Protein-Coupled metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1873-3913
- Volume :
- 41
- Database :
- MEDLINE
- Journal :
- Cellular signalling
- Publication Type :
- Academic Journal
- Accession number :
- 28389415
- Full Text :
- https://doi.org/10.1016/j.cellsig.2017.04.002