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Cardiovascular Research 2003 57(2):358-369; doi:10.1016/S0008-6363(02)00660-0
© 2003 by European Society of Cardiology
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Copyright © 2003, European Society of Cardiology

Caveolin-1 and -3 dissociations from caveolae to cytosol in the heart during aging and after myocardial infarction in rat

Philippe Ratajczaka, Thibaud Damya, Christophe Heymesa, Patricia Oliviéroa, Françoise Marottea, Estelle Robidela, Richard Sercombeb, Jorge Boczkowskic, Lydie Rappaporta and Jane-Lise Samuela,*

aInserm-U572/IFR 6, Hopital Lariboisière, 41 Boulevard de la Chapelle, 75475 Paris Cedex 10, France
bCNRS-UPR 646/IFR 6, Faculté de médecine Lariboisière, Saint-Louis, IFR 6, France
cInserm U408, Hôpital Bichat Université D Diderot, Paris, France

* Corresponding author. Tel.: +33-144-631-735; fax: +331-48-742-315 janelyse.samuel{at}inserm.lrb.ap-hop-paris.fr

Objective: Caveolins, the structural proteins of caveolae, modulate numerous signaling pathways including Nitric Oxide (NO) production. Among the caveolin family, caveolin-1 and -3 are mainly expressed in endothelial and muscle cells, respectively. In this study, we investigate whether (i) changes in caveolin abundance and/or distribution occur during cardiac aging and failure in rat, and (ii) the process could influence NO synthase (NOS) activity. Methods: Using immunohistolabelling and Western blot approaches, expression and distribution of caveolins were analysed in adult (Ad), senescent (S-Sh) and myocardial infarction-induced failing (S-MI) hearts. NOS3/caveolin-1 interactions were evaluated by immunoprecipitation assays. Results: At the microscope level, caveolin-1 distribution in the endothelial cells was unchanged between the groups. Conversely the typical distribution of caveolin-3 in myocyte sarcolemma was dramatically altered in S-MI rats, resulting in a heterogeneous pattern throughout the septum. Total abundance of caveolin-1 and -3 remained stable whatever the group. In the fractions free of caveolae (Triton X-100 soluble), the levels of caveolin-1{alpha} and -3 increased with aging (+20%, and +104%, P<0.05 versus Ad, respectively) and were further enhanced in S-MI (+25%, +30%, P<0.05, P<0.001 versus S-Sh respectively). In these fractions, NOS3/caveolin-1{alpha} complexes increased as well. In addition, NOS activity was negatively correlated to caveolin-1 level in the cytosolic fractions. Conclusions: We demonstrate that dissociation of caveolin from caveolae is associated with aging and heart failure, the process being related to the decreased NOS activity.

KEYWORDS Aging; Capillaries; Heart failure; Sarcolemma


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