Integrating GRK2 and NFkappaB in the Pathophysiology of Cardiac Hypertrophy.

Authors:
Daniela Sorriento
Daniela Sorriento
Department of Clinical Medicine
Italy
Gaetano Santulli
Gaetano Santulli
Federico II University of Naples
Italy
Antonietta Franco
Antonietta Franco
Washington University School of Medicine
Italy
Ersilia Cipolletta
Ersilia Cipolletta
Department of Clinical Medicine
Italy

J Cardiovasc Transl Res 2015 Nov 30;8(8):493-502. Epub 2015 Jul 30.

Department of Medicine and Surgery, University of Salerno, Via Salvador Allende, 84081, Baronissi, SA, Italy.

G protein coupled receptor kinase type 2 (GRK2) plays an important role in the development and maintenance of cardiac hypertrophy and heart failure even if its exact role is still unknown. In this study, we assessed the effect of GRK2 on the regulation of cardiac hypertrophy. In H9C2 cells, GRK2 overexpression increased atrial natriuretic factor (ANF) activity and enhanced phenylephrine-induced ANF response, and this is associated with an increase of NFκB transcriptional activity. The kinase dead mutant and a synthetic inhibitor of GRK2 activity exerted the opposite effect, suggesting that GRK2 regulates hypertrophy through upregulation of NFκB activity in a phosphorylation-dependent manner. In two different in vivo models of left ventricle hypertrophy (LVH), the selective inhibition of GRK2 activity prevented hypertrophy and reduced NFκB transcription activity. Our results suggest a previously undisclosed role for GRK2 in the regulation of hypertrophic responses and propose GRK2 as potential therapeutic target for limiting LVH.

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http://dx.doi.org/10.1007/s12265-015-9646-0DOI Listing
November 2015
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