TY - JOUR
T1 - GRK mythology
T2 - G-protein receptor kinases in cardiovascular disease
AU - Dorn, Gerald W.
PY - 2009/5
Y1 - 2009/5
N2 - G-protein receptor kinases (GRKs) are indispensable for terminating signaling of G-protein coupled receptors (GPCR) through receptor desensitization and downregulation. Increased neurohormone levels in heart failure and the adverse consequences of constant neurohormonal stimulation suggest an important protective role for mechanisms that desensitize neurohormone receptor responses. For that reason, GRK2, the first GRK identified in the heart, has been extensively studied in heart failure, cardiac hypertrophy, and myocardial infarction. However, our understanding of the roles of GRKs in general, and the differential effects of cardiac receptor phosphorylation by individual cardiac-expressed GRKs, have evolved considerably in the last few years. Here, recent developments are reviewed, with an emphasis on novel GRK functions and signaling pathways.
AB - G-protein receptor kinases (GRKs) are indispensable for terminating signaling of G-protein coupled receptors (GPCR) through receptor desensitization and downregulation. Increased neurohormone levels in heart failure and the adverse consequences of constant neurohormonal stimulation suggest an important protective role for mechanisms that desensitize neurohormone receptor responses. For that reason, GRK2, the first GRK identified in the heart, has been extensively studied in heart failure, cardiac hypertrophy, and myocardial infarction. However, our understanding of the roles of GRKs in general, and the differential effects of cardiac receptor phosphorylation by individual cardiac-expressed GRKs, have evolved considerably in the last few years. Here, recent developments are reviewed, with an emphasis on novel GRK functions and signaling pathways.
KW - Adrenergic receptors
KW - Cell signaling
KW - G-protein receptor kinases
KW - Heart failure
KW - Myocardial infarction
UR - http://www.scopus.com/inward/record.url?scp=67349181755&partnerID=8YFLogxK
U2 - 10.1007/s00109-009-0450-7
DO - 10.1007/s00109-009-0450-7
M3 - Review article
C2 - 19229505
AN - SCOPUS:67349181755
SN - 0946-2716
VL - 87
SP - 455
EP - 463
JO - Journal of Molecular Medicine
JF - Journal of Molecular Medicine
IS - 5
ER -