Multivalent dendrimeric and monomeric adenosine agonists attenuate cell death in HL-1 mouse cardiomyocytes expressing the A3 receptor |
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Authors: | Athena M. Keene Ramachandran Balasubramanian Asher Shainberg |
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Affiliation: | a Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0810, USA b Mass Spectrometry Facility, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892-0810, USA c Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel |
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Abstract: | Multivalent dendrimeric conjugates of GPCR ligands may have increased potency or selectivity in comparison to monomeric ligands, a phenomenon that was tested in a model of cytoprotection in mouse HL-1 cardiomyocytes. Quantitative RT-PCR indicated high expression levels of endogenous A1 and A2A adenosine receptors (ARs), but not of A2B and A3ARs. Activation of the heterologously expressed human A3AR in HL-1 cells by AR agonists significantly attenuated cell damage following 4 h exposure to H2O2 (750 μM) but not in untransfected cells. The A3 agonist IB-MECA (EC50 3.8 μM) and the non-selective agonist NECA (EC50 3.9 μM) protected A3 AR-transfected cells against H2O2 in a concentration-dependent manner, as determined by lactate dehydrogenase release. A generation 5.5 PAMAM (polyamidoamine) dendrimeric conjugate of a N6-chain-functionalized adenosine agonist was synthesized and its mass indicated an average of 60 amide-linked nucleoside moieties out of 256 theoretical attachment sites. It non-selectively activated the A3AR to inhibit forskolin-stimulated cAMP formation (IC50 66 nM) and, similarly, protected A3-transfected HL-1 cells from apoptosis-inducing H2O2 with greater potency (IC50 35 nM) than monomeric nucleosides. Thus, a PAMAM conjugate retained AR binding affinity and displayed greatly enhanced cardioprotective potency. |
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Keywords: | ADAC, N6-[4-[[[4-[[[(2-aminoethyl)amino]carbonyl]methyl]-anilino]carbonyl]methyl]phenyl]adenosine AF488, Alexa-Fluor® 488 CHAPS, 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate hydrate CHO, Chinese hamster ovary Cl-IB-MECA, 2-chloro-N6-(3-iodobenzyl)-5&prime -N-methylcarboxamidoadenosine DMEM, Dulbecco's modified Eagle medium DMF, N,N-dimethylformamide DMSO, dimethyl sulfoxide ED, ethylenediamine EDC, N-(3-dimethylaminopropyl)-N&prime -ethylcarbodiimide EDTA, ethylenediaminetetraacetic acid FBS, fetal bovine serum [3H]CGS21680, 2-[p-(2-carboxyethyl)phenylethyl-amino]-5&prime -N-ethylcarboxamido-adenosine GPCR, G protein-coupled receptor HEK, human embryonic kidney HEPES, 4-(2-hydroxyethyl)-1-piperazineethanesulfonic acid [125I]AB-MECA, [125I]-4-aminobenzyl-5&prime -N-methylcarboxamidoadenosine IB-MECA, N6-(3-iodobenzyl)-5&prime -N-methylcarboxamidoadenosine MALDI-TOF, matrix assisted laser desorption/ionization time-of-flight MES, 2-(N-morpholino)ethanesulfonic acid MS, mass spectrometry NMR, nuclear magnetic resonance PAMAM, polyamidoamine qRT-PCR, quantitative real-time polymerase chain reaction |
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