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      Effects of cholesterol depletion on compartmentalized cAMP responses in adult cardiac myocytes

      research-article
      a , b , a , b , b , a , *
      Journal of Molecular and Cellular Cardiology
      Academic Press
      AKAP, A kinase anchoring protein, βAR, beta adrenergic receptor, cAMP, cyclic adenosine monophosphate, Cav-3, caveolin-3, PKA, protein kinase A, CGP, CGP20712A, Epac2, exchange protein activated by cAMP, EPR, E-type prostaglandin receptor, FRET, fluorescence resonance energy transfer, IBMX, 3-isobutyl-1- methylxanthine, ICa-L, L-type Ca2+ current, ICI, ICI118,551, Iso, isoproterenol bitartrate, MβCD, methyl-β-cyclodextrin, PKA, protein kinase A, PGE1, prostaglandin E1, cAMP compartmentation, Lipid rafts, Adult ventricular myocytes

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          Abstract

          β 1-Adrenergic receptors (β 1ARs) and E-type prostaglandin receptors (EPRs) both produce compartmentalized cAMP responses in cardiac myocytes. The role of cholesterol-dependent lipid rafts in producing these compartmentalized responses was investigated in adult rat ventricular myocytes. β 1ARs were found in lipid raft and non-lipid raft containing membrane fractions, while EPRs were only found in non-lipid raft fractions. Furthermore, β 1AR activation enhanced the L-type Ca 2+ current, intracellular Ca 2+ transient, and myocyte shortening, while EPR activation had no effect, consistent with the idea that these functional responses are regulated by cAMP produced by receptors found in lipid raft domains. Using methyl-β-cyclodextrin to disrupt lipid rafts by depleting membrane cholesterol did not eliminate compartmentalized behavior, but it did selectively alter specific receptor-mediated responses. Cholesterol depletion enhanced the sensitivity of functional responses produced by β 1ARs without having any effect on EPR activation. Changes in cAMP activity were also measured in intact cells using two different FRET-based biosensors: a type II PKA-based probe to monitor cAMP in subcellular compartments that include microdomains associated with caveolar lipid rafts and a freely diffusible Epac2-based probe to monitor total cytosolic cAMP. β 1AR and EPR activation elicited responses detected by both FRET probes. However, cholesterol depletion only affected β 1AR responses detected by the PKA probe. These results indicate that lipid rafts alone are not sufficient to explain the difference between β 1AR and EPR responses. They also suggest that β 1AR regulation of myocyte contraction involves the local production of cAMP by a subpopulation of receptors associated with caveolar lipid rafts.

          Research Highlights

          ► Not all cAMP coupled receptors produce functional responses in adult cardiac myocytes. ► Functional responses correlate with receptors found in lipid rafts domains. ► Lipid raft receptors stimulate local cAMP production detected in PKA signaling domains. ► Non-lipid raft receptors produced cAMP detected outside of PKA signaling domains. ► Cholesterol depletion alters lipid raft dependent responses but not compartmentation.

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          Most cited references41

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          Lipid raft microdomains and neurotransmitter signalling.

          Lipid rafts are specialized structures on the plasma membrane that have an altered lipid composition as well as links to the cytoskeleton. It has been proposed that these structures are membrane domains in which neurotransmitter signalling might occur through a clustering of receptors and components of receptor-activated signalling cascades. The localization of these proteins in lipid rafts, which is affected by the cytoskeleton, also influences the potency and efficacy of neurotransmitter receptors and transporters. The effect of lipid rafts on neurotransmitter signalling has also been implicated in neurological and psychiatric diseases.
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            Novel single chain cAMP sensors for receptor-induced signal propagation.

            cAMP is a universal second messenger of many G-protein-coupled receptors and regulates a wide variety of cellular events. cAMP exerts its effects via cAMP-dependent protein kinase (PKA), cAMP-gated ion channels, and two isoforms of exchange protein directly activated by cAMP (Epac). Here we report the development of novel fluorescent indicators for cAMP based on the cAMP-binding domains of Epac and PKA. Fluorescence resonance energy transfer between variants of green fluorescent protein (enhanced cyan fluorescent protein and enhanced yellow fluorescent protein) fused directly to the cAMP-binding domains was used to analyze spatial and temporal aspects of cAMP-signaling in different cells. In contrast to previously developed PKA-based indicators, these probes are comprised of only a single binding site lacking cooperativity, catalytic properties, and interactions with other proteins and thereby allow us to easily image free intracellular cAMP and rapid signaling events. Rapid beta-adrenergic receptor-induced cAMP signals were observed to travel with high speed ( approximately 40 microm/s) throughout the entire cell body of hippocampal neurons and peritoneal macrophages. The developed indicators could be ubiquitously applied to studying cAMP, its physiological role and spatio-temporal regulation.
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              Role of caveolae and caveolins in health and disease.

              Although they were discovered more than 50 years ago, caveolae have remained enigmatic plasmalemmal organelles. With their characteristic "flasklike" shape and virtually ubiquitous tissue distribution, these interesting structures have been implicated in a wide range of cellular functions. Similar to clathrin-coated pits, caveolae function as macromolecular vesicular transporters, while their unique lipid composition classifies them as plasma membrane lipid rafts, structures enriched in a variety of signaling molecules. The caveolin proteins (caveolin-1, -2, and -3) serve as the structural components of caveolae, while also functioning as scaffolding proteins, capable of recruiting numerous signaling molecules to caveolae, as well as regulating their activity. That so many signaling molecules and signaling cascades are regulated by an interaction with the caveolins provides a paradigm by which numerous disease processes may be affected by ablation or mutation of these proteins. Indeed, studies in caveolin-deficient mice have implicated these structures in a host of human diseases, including diabetes, cancer, cardiovascular disease, atherosclerosis, pulmonary fibrosis, and a variety of degenerative muscular dystrophies. In this review, we provide an in depth summary regarding the mechanisms by which caveolae and caveolins participate in human disease processes.
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                Author and article information

                Journal
                J Mol Cell Cardiol
                J. Mol. Cell. Cardiol
                Journal of Molecular and Cellular Cardiology
                Academic Press
                0022-2828
                1095-8584
                March 2011
                March 2011
                : 50
                : 3
                : 500-509
                Affiliations
                [a ]Department of Pharmacology—MS318, University of Nevada School of Medicine, Reno, NV 89557, USA
                [b ]Institute of Membrane and Systems Biology, University of Leeds, Leeds LS2 9JT, UK
                Author notes
                [* ]Corresponding author. Tel.: +1 775 784 4119; fax: +1 775 784 1620. rdharvey@ 123456medicine.nevada.edu
                Article
                YJMCC6970
                10.1016/j.yjmcc.2010.11.015
                3049871
                21115018
                20534ad1-5881-4f79-90f2-2fccac9cf0b1
                © 2011 Elsevier Ltd.

                This document may be redistributed and reused, subject to certain conditions.

                History
                : 19 August 2010
                : 27 October 2010
                : 16 November 2010
                Categories
                Original Article

                Cardiovascular Medicine
                βar, beta adrenergic receptor,pge1, prostaglandin e1,mβcd, methyl-β-cyclodextrin,ibmx, 3-isobutyl-1- methylxanthine,epac2, exchange protein activated by camp,cgp, cgp20712a,adult ventricular myocytes,camp, cyclic adenosine monophosphate,iso, isoproterenol bitartrate,cav-3, caveolin-3,fret, fluorescence resonance energy transfer,akap, a kinase anchoring protein,ici, ici118,551,ica-l, l-type ca2+ current,camp compartmentation,lipid rafts,epr, e-type prostaglandin receptor,pka, protein kinase a

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