Literature DB >> 10771510

Characterization of caveolae from rat heart: localization of postreceptor signal transduction molecules and their rearrangement after norepinephrine stimulation.

A De Luca1, M Sargiacomo, A Puca, G Sgaramella, P De Paolis, G Frati, C Morisco, B Trimarco, M Volpe, G Condorelli.   

Abstract

Caveolae are plasma membrane subcompartments that have been implicated in signal transduction. In many cellular systems, caveolae are rich in signal transduction molecules such as G proteins and receptor-associated tyrosine kinases. An important structural component of the caveolae is caveolin. Recent evidence show that among the caveolin gene family, caveolin-3 is expressed in skeletal and cardiac muscle and caveolae are present in cardiac myocyte cells. Both the ANP receptor as well as the muscarinic receptor have been localized to the caveolae of cardiac myocytes in culture. These findings prompted us to conduct a further analysis of cardiac caveolae. In order to improve our understanding of the mechanisms of signal transduction regulation in cardiac myocytes, we isolated cardiac caveolae by discontinuous sucrose density gradient centrifugation from rat ventricles and rat neonatal cardiocytes. Our analysis of caveolar content demonstrates that heterotrimeric G proteins, p21ras and receptor-associated tyrosine kinases are concentrated within these structures. We also show that adrenergic stimulation induces an increase in the amount of diverse alpha- and beta-subunits of G proteins, as well as p21ras, in both in vivo and in vitro experimental settings. Our data show that cardiac caveolae are an important site of signal transduction regulation. This finding suggests a potential role for these structures in physiological and pathological states. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10771510     DOI: 10.1002/(sici)1097-4644(20000615)77:4<529::aid-jcb2>3.3.co;2-o

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  5 in total

1.  Cardiomyocytes induce endothelial cells to trans-differentiate into cardiac muscle: implications for myocardium regeneration.

Authors:  G Condorelli; U Borello; L De Angelis; M Latronico; D Sirabella; M Coletta; R Galli; G Balconi; A Follenzi; G Frati; M G Cusella De Angelis; L Gioglio; S Amuchastegui; L Adorini; L Naldini; A Vescovi; E Dejana; G Cossu
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-04       Impact factor: 11.205

2.  Clonally expanded novel multipotent stem cells from human bone marrow regenerate myocardium after myocardial infarction.

Authors:  Young-sup Yoon; Andrea Wecker; Lindsay Heyd; Jong-Seon Park; Tengiz Tkebuchava; Kengo Kusano; Allison Hanley; Heather Scadova; Gangjian Qin; Dong-Hyun Cha; Kirby L Johnson; Ryuichi Aikawa; Takayuki Asahara; Douglas W Losordo
Journal:  J Clin Invest       Date:  2005-02       Impact factor: 14.808

3.  The role of PKCε-dependent signaling for cardiac differentiation.

Authors:  D Galli; G Gobbi; C Carrubbi; D Di Marcantonio; L Benedetti; M G C De Angelis; T Meschi; M Vaccarezza; M Sampaolesi; P Mirandola; M Vitale
Journal:  Histochem Cell Biol       Date:  2012-08-31       Impact factor: 4.304

4.  Regulation of cardiac contractility by Rab4-modulated beta2-adrenergic receptor recycling.

Authors:  Amy Odley; Harvey S Hahn; Roy A Lynch; Yehia Marreez; Hanna Osinska; Jeffrey Robbins; Gerald W Dorn
Journal:  Proc Natl Acad Sci U S A       Date:  2004-04-22       Impact factor: 11.205

5.  High Efficacy but Low Potency of δ-Opioid Receptor-G Protein Coupling in Brij-58-Treated, Low-Density Plasma Membrane Fragments.

Authors:  Lenka Roubalova; Miroslava Vosahlikova; Jana Brejchova; Jan Sykora; Vladimir Rudajev; Petr Svoboda
Journal:  PLoS One       Date:  2015-08-18       Impact factor: 3.240

  5 in total

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