Medizinische Universität Graz - Research portal

Logo MUG Resarch Portal

Selected Publication:

Mittmann, C; Chung, CH; Höppner, G; Michalek, C; Nose, M; Schüler, C; Schuh, A; Eschenhagen, T; Weil, J; Pieske, B; Hirt, S; Wieland, T.
Expression of ten RGS proteins in human myocardium: functional characterization of an upregulation of RGS4 in heart failure.
Cardiovasc Res. 2002; 55(4):778-786 Doi: 10.1016/S0008-6363(02)00459-5 [OPEN ACCESS]
Web of Science PubMed FullText FullText_MUG Google Scholar

 

Co-authors Med Uni Graz
Pieske Burkert Mathias
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
OBJECTIVE: RGS proteins (regulators of G protein signalling) negatively regulate G protein function as GTPase activating proteins. By controlling heterotrimeric G proteins they may regulate myocardial hypertrophy and contractility. We investigated the expression of RGS proteins in the human heart and whether they take part in the pathophysiological changes of heart failure. METHODS AND RESULTS: Using RNase protection assays (RPAs) RGS2, 3L, 3S, 4, 5 and 6 were identified in the myocardium from terminally failing human hearts with dilated (DCM, n=22) or ischemic (ICM, n=18) cardiomyopathy and from nonfailing donor hearts (NF, n=9). With reverse transcriptase polymerase chain reaction in addition mRNA of RGS1, 9, 12, 14 and 16 were detectable. Compared to NF in failing LV myocardium RGS4 mRNA and protein was upregulated 2-3-fold (mRNA, 10(-21) mol/microg+/-S.E.M.: NF: 22+/-5, DCM: 51+/-10*, ICM: 37+/-8; P<0.05 vs. DCM+ICM, *P<0.05 vs. NF, P<0.05 vs. DCM+ICM; protein, % of NF+/-S.E.M.: NF: 100+/-35, DCM 266+/-60*, ICM: 205+/-64, n=5, *P<0.05 vs. NF). In contrast, RGS2, 3L, 3S, 5, 6, and 16 protein and mRNA levels did not vary between failing and NF hearts. In order to investigate the impact of RGS4 on Gq/11 mediated signalling, PLC activity was measured in human LV membranes. Recombinant RGS4 blunted the endothelin-1 (ET-1) stimulated PLC activity. When overexpressed by adenoviral mediated gene transfer in rabbit ventricular myocytes RGS4 abolished the inotropic effect of ET-1. CONCLUSION: The upregulation of RGS4 in failing human myocardium diminishes Gq/11-mediated signalling and can be involved in the desensitization of Gq/11-mediated positive inotropic effects.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Blotting, Western -
Case-Control Studies -
Female -
GTP-Binding Proteins -
GTPase-Activating Proteins -
Gene Expression -
Gene Expression Regulation -
Heart Failure, Congestive - metabolism
Heart Ventricles - metabolism
Humans - metabolism
Middle Aged - metabolism
Myocardial Contraction - physiology
Myocardium - chemistry
Proteins - analysis
RGS Proteins - analysis
RNA, Messenger - analysis
Rabbits - analysis
Reverse Transcriptase Polymerase Chain Reaction - analysis

Find related publications in this database (Keywords)
contractile function
endothelins
G-proteins
heart failure
myocytes
© Med Uni GrazImprint