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Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†

[Image: see text] The triadin isoforms Trisk 95 and Trisk 51 are both components of the skeletal muscle calcium release complex. To investigate the specific role of Trisk 95 and Trisk 51 isoforms in muscle physiology, we overexpressed Trisk 95 or Trisk 51 using adenovirus-mediated gene transfer in s...

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Autores principales: Vassilopoulos, Stéphane, Oddoux, Sarah, Groh, Séverine, Cacheux, Marine, Fauré, Julien, Brocard, Julie, Campbell, Kevin P., Marty, Isabelle
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2010
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907096/
https://www.ncbi.nlm.nih.gov/pubmed/20565104
http://dx.doi.org/10.1021/bi100796v
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author Vassilopoulos, Stéphane
Oddoux, Sarah
Groh, Séverine
Cacheux, Marine
Fauré, Julien
Brocard, Julie
Campbell, Kevin P.
Marty, Isabelle
author_facet Vassilopoulos, Stéphane
Oddoux, Sarah
Groh, Séverine
Cacheux, Marine
Fauré, Julien
Brocard, Julie
Campbell, Kevin P.
Marty, Isabelle
author_sort Vassilopoulos, Stéphane
collection PubMed
description [Image: see text] The triadin isoforms Trisk 95 and Trisk 51 are both components of the skeletal muscle calcium release complex. To investigate the specific role of Trisk 95 and Trisk 51 isoforms in muscle physiology, we overexpressed Trisk 95 or Trisk 51 using adenovirus-mediated gene transfer in skeletal muscle of newborn mice. Overexpression of either Trisk 95 or Trisk 51 alters the muscle fiber morphology, while leaving unchanged the expression of the ryanodine receptor, the dihydropyridine receptor, and calsequestrin. We also observe an aberrant expression of caveolin 3 in both Trisk 95- and Trisk 51-overexpressing skeletal muscles. Using a biochemical approach, we demonstrate that caveolin 3 is associated with the calcium release complex in skeletal muscle. Taking advantage of muscle and non-muscle cell culture models and triadin null mouse skeletal muscle, we further dissect the molecular organization of the caveolin 3-containing calcium release complex. Our data demonstrate that the association of caveolin 3 with the calcium release complex occurs via a direct interaction with the transmembrane domain of the ryanodine receptor. Taken together, these data suggest that caveolin 3-containing membrane domains and the calcium release complex are functionally linked and that Trisk 95 and Trisk 51 are instrumental to the regulation of this interaction, the integrity of which may be crucial for muscle physiology.
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spelling pubmed-29070962010-07-20 Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification† Vassilopoulos, Stéphane Oddoux, Sarah Groh, Séverine Cacheux, Marine Fauré, Julien Brocard, Julie Campbell, Kevin P. Marty, Isabelle Biochemistry [Image: see text] The triadin isoforms Trisk 95 and Trisk 51 are both components of the skeletal muscle calcium release complex. To investigate the specific role of Trisk 95 and Trisk 51 isoforms in muscle physiology, we overexpressed Trisk 95 or Trisk 51 using adenovirus-mediated gene transfer in skeletal muscle of newborn mice. Overexpression of either Trisk 95 or Trisk 51 alters the muscle fiber morphology, while leaving unchanged the expression of the ryanodine receptor, the dihydropyridine receptor, and calsequestrin. We also observe an aberrant expression of caveolin 3 in both Trisk 95- and Trisk 51-overexpressing skeletal muscles. Using a biochemical approach, we demonstrate that caveolin 3 is associated with the calcium release complex in skeletal muscle. Taking advantage of muscle and non-muscle cell culture models and triadin null mouse skeletal muscle, we further dissect the molecular organization of the caveolin 3-containing calcium release complex. Our data demonstrate that the association of caveolin 3 with the calcium release complex occurs via a direct interaction with the transmembrane domain of the ryanodine receptor. Taken together, these data suggest that caveolin 3-containing membrane domains and the calcium release complex are functionally linked and that Trisk 95 and Trisk 51 are instrumental to the regulation of this interaction, the integrity of which may be crucial for muscle physiology. American Chemical Society 2010-06-21 2010-07-27 /pmc/articles/PMC2907096/ /pubmed/20565104 http://dx.doi.org/10.1021/bi100796v Text en Copyright © 2010 American Chemical Society http://pubs.acs.orgThis is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Vassilopoulos, Stéphane
Oddoux, Sarah
Groh, Séverine
Cacheux, Marine
Fauré, Julien
Brocard, Julie
Campbell, Kevin P.
Marty, Isabelle
Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
title Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
title_full Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
title_fullStr Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
title_full_unstemmed Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
title_short Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
title_sort caveolin 3 is associated with the calcium release complex and is modified via in vivo triadin modification†
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2907096/
https://www.ncbi.nlm.nih.gov/pubmed/20565104
http://dx.doi.org/10.1021/bi100796v
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