Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice

Duchenne muscular dystrophy (DMD) and murine X-linked muscular dystrophy (mdx), its murine model, are characterized by muscle damage and muscle weakness associated with inflammation and new vessel formation. Caveolins, dystrophin-associated proteins, are involved in the pathogenesis of DMD, because...

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Main Authors: Alexander Spassov, Tomasz Gedrange, Katarzyna Sporniak-Tutak, Agnieszka Mielczarek, Sven Morgenstern, Silke Lucke, Tomasz Gredes, Christiane Kunert-Keil
Format: Article
Language:English
Published: Via Medica 2011-07-01
Series:Folia Histochemica et Cytobiologica
Subjects:
Online Access:http://czasopisma.viamedica.pl/fhc/article/view/4127
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author Alexander Spassov
Tomasz Gedrange
Katarzyna Sporniak-Tutak
Agnieszka Mielczarek
Sven Morgenstern
Silke Lucke
Tomasz Gredes
Christiane Kunert-Keil
author_facet Alexander Spassov
Tomasz Gedrange
Katarzyna Sporniak-Tutak
Agnieszka Mielczarek
Sven Morgenstern
Silke Lucke
Tomasz Gredes
Christiane Kunert-Keil
author_sort Alexander Spassov
collection DOAJ
description Duchenne muscular dystrophy (DMD) and murine X-linked muscular dystrophy (mdx), its murine model, are characterized by muscle damage and muscle weakness associated with inflammation and new vessel formation. Caveolins, dystrophin-associated proteins, are involved in the pathogenesis of DMD, because increased numbers of caveolae are found in DMD and mdx hindlimb muscles. Caveolae influence angiogenesis due to their content of vascular endothelial growth factor (VEGF) receptors. Orofacial muscles in mdx mice undergo muscle necrosis followed by muscle regeneration. To ascertain the role of caveolins and VEGF in the pathogenesis of dystrophic masticatory muscles, we examined the expression of caveolin-1 (cav-1), caveolin-3 (cav-3) and VEGF in control and mdx mice. In mdx masticatory muscles, no changes in transcript and protein levels of VEGF were found, whereas cav-1 and cav-3 expression was increased. Using immunohistochemistry, a strong sarcolemmal staining of caveolin-3 in regenerated muscle fibers was found. Furthermore, immunohistochemistry with the caveolin-1 antibody showed an increase in the amount of blood vessels in areas with regenerating muscle fibers. Dystrophic masticatory muscles showed changes comparable to those of hindlimb muscles in the expression of cav-1 and cav-3. The angiogenesis seems to be unaffected in the jaw muscles of mdx mice. We speculate that the increased caveolin expression could cause extensive and efficient muscle regeneration. (Folia Histochemica et Cytobiologica 2011; Vol. 49, No. 2, pp. 291–298)
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spelling doaj.art-4d20aa8dac9549bd9d94532869bbeea52022-12-22T02:36:59ZengVia MedicaFolia Histochemica et Cytobiologica0239-85081897-56312011-07-0149229129810.5603/4127Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx miceAlexander SpassovTomasz GedrangeKatarzyna Sporniak-TutakAgnieszka MielczarekSven MorgensternSilke LuckeTomasz GredesChristiane Kunert-KeilDuchenne muscular dystrophy (DMD) and murine X-linked muscular dystrophy (mdx), its murine model, are characterized by muscle damage and muscle weakness associated with inflammation and new vessel formation. Caveolins, dystrophin-associated proteins, are involved in the pathogenesis of DMD, because increased numbers of caveolae are found in DMD and mdx hindlimb muscles. Caveolae influence angiogenesis due to their content of vascular endothelial growth factor (VEGF) receptors. Orofacial muscles in mdx mice undergo muscle necrosis followed by muscle regeneration. To ascertain the role of caveolins and VEGF in the pathogenesis of dystrophic masticatory muscles, we examined the expression of caveolin-1 (cav-1), caveolin-3 (cav-3) and VEGF in control and mdx mice. In mdx masticatory muscles, no changes in transcript and protein levels of VEGF were found, whereas cav-1 and cav-3 expression was increased. Using immunohistochemistry, a strong sarcolemmal staining of caveolin-3 in regenerated muscle fibers was found. Furthermore, immunohistochemistry with the caveolin-1 antibody showed an increase in the amount of blood vessels in areas with regenerating muscle fibers. Dystrophic masticatory muscles showed changes comparable to those of hindlimb muscles in the expression of cav-1 and cav-3. The angiogenesis seems to be unaffected in the jaw muscles of mdx mice. We speculate that the increased caveolin expression could cause extensive and efficient muscle regeneration. (Folia Histochemica et Cytobiologica 2011; Vol. 49, No. 2, pp. 291–298)http://czasopisma.viamedica.pl/fhc/article/view/4127mdx micemuscular dystrophyhistopathologymasticatory muscles
spellingShingle Alexander Spassov
Tomasz Gedrange
Katarzyna Sporniak-Tutak
Agnieszka Mielczarek
Sven Morgenstern
Silke Lucke
Tomasz Gredes
Christiane Kunert-Keil
Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice
Folia Histochemica et Cytobiologica
mdx mice
muscular dystrophy
histopathology
masticatory muscles
title Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice
title_full Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice
title_fullStr Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice
title_full_unstemmed Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice
title_short Caveolin-1, caveolin-3 and VEGF expression in the masticatory muscles of mdx mice
title_sort caveolin 1 caveolin 3 and vegf expression in the masticatory muscles of mdx mice
topic mdx mice
muscular dystrophy
histopathology
masticatory muscles
url http://czasopisma.viamedica.pl/fhc/article/view/4127
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