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Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane

Mutations in or ablation of the gene encoding caveolin-3, a protein of muscle cell caveolae, result in forms of muscular dystrophy and cardiomyopathy. Another member of the caveolin gene family, caveolin-1, is widely considered not to be expressed in myocytes, yet ablation of the gene encoding this...

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Autores principales: Robenek, Horst, Weissen-Plenz, Gabriele, Severs, Nicholas J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Ltd 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514129/
https://www.ncbi.nlm.nih.gov/pubmed/18793348
http://dx.doi.org/10.1111/j.1582-4934.2008.00498.x
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author Robenek, Horst
Weissen-Plenz, Gabriele
Severs, Nicholas J
author_facet Robenek, Horst
Weissen-Plenz, Gabriele
Severs, Nicholas J
author_sort Robenek, Horst
collection PubMed
description Mutations in or ablation of the gene encoding caveolin-3, a protein of muscle cell caveolae, result in forms of muscular dystrophy and cardiomyopathy. Another member of the caveolin gene family, caveolin-1, is widely considered not to be expressed in myocytes, yet ablation of the gene encoding this protein in mice also results in cardiomyopathy. By applying the high-resolution electron-microscopical imaging technique of freeze-fracture replica immunolabelling, we report here evidence that caveolin-1 is expressed in human cardiac myocytes, localized to both caveolae and non-caveolar domains in the plasma membrane. Disorders of the myocyte resulting from defects in caveolin-1 may thus arise directly, at the level of the myocyte, rather than via other cell types as previously proposed.
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spelling pubmed-45141292015-07-27 Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane Robenek, Horst Weissen-Plenz, Gabriele Severs, Nicholas J J Cell Mol Med Images in Cellular/Molecular Medicine Mutations in or ablation of the gene encoding caveolin-3, a protein of muscle cell caveolae, result in forms of muscular dystrophy and cardiomyopathy. Another member of the caveolin gene family, caveolin-1, is widely considered not to be expressed in myocytes, yet ablation of the gene encoding this protein in mice also results in cardiomyopathy. By applying the high-resolution electron-microscopical imaging technique of freeze-fracture replica immunolabelling, we report here evidence that caveolin-1 is expressed in human cardiac myocytes, localized to both caveolae and non-caveolar domains in the plasma membrane. Disorders of the myocyte resulting from defects in caveolin-1 may thus arise directly, at the level of the myocyte, rather than via other cell types as previously proposed. John Wiley & Sons, Ltd 2008-12 2008-09-13 /pmc/articles/PMC4514129/ /pubmed/18793348 http://dx.doi.org/10.1111/j.1582-4934.2008.00498.x Text en © 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Images in Cellular/Molecular Medicine
Robenek, Horst
Weissen-Plenz, Gabriele
Severs, Nicholas J
Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
title Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
title_full Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
title_fullStr Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
title_full_unstemmed Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
title_short Freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
title_sort freeze-fracture replica immunolabelling reveals caveolin-1 in the human cardiomyocyte plasma membrane
topic Images in Cellular/Molecular Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514129/
https://www.ncbi.nlm.nih.gov/pubmed/18793348
http://dx.doi.org/10.1111/j.1582-4934.2008.00498.x
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