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Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles

PURPOSE: To compare the organization of human and rat ocular medial recti muscles (MR). METHODS: The cryosections of human and rat MR were processed for myofibrillar ATPase (mATPase), succinate dehydrogenase and glycerol-3-phosphate dehydrogenase. To reveal myosin heavy chain (MyHC) isoforms, specif...

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Autores principales: Stirn Kranjc, Branka, Smerdu, Vika, Eržen, Ida
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758108/
https://www.ncbi.nlm.nih.gov/pubmed/19609551
http://dx.doi.org/10.1007/s00417-009-1128-0
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author Stirn Kranjc, Branka
Smerdu, Vika
Eržen, Ida
author_facet Stirn Kranjc, Branka
Smerdu, Vika
Eržen, Ida
author_sort Stirn Kranjc, Branka
collection PubMed
description PURPOSE: To compare the organization of human and rat ocular medial recti muscles (MR). METHODS: The cryosections of human and rat MR were processed for myofibrillar ATPase (mATPase), succinate dehydrogenase and glycerol-3-phosphate dehydrogenase. To reveal myosin heavy chain (MyHC) isoforms, specific monoclonal antibodies against MyHC-1/β- slow, α-cardiac (-α), -2a, -2x, -2b, -extraocular (eom), -embryonic (-emb) and -neonatal (-neo) were applied. The MyHC gene expression was studied by in situ hybridization in human muscle. RESULTS: The muscle fibers were arranged in two distinct layers in both species. In the orbital layer most fibers were highly oxidative and expressed fast MyHC isoforms, whereas slow and oxidative fibers expressed MyHC-1 and -α, some of them also MyHC-2a, -2x, -eom, very rarely -emb, and –neo. In the global layer, slow fibers with very low oxidative and glycolytic activity and three types of fast fibers, glycolytic, oxidative and oxidative-glycolytic, could be distinguished. The slow medium-sized fibers with mATPase activity stable at pH 4.4 expressed mostly MyHC-1 and -α in rat, while in humans they co-expressed MyHC-1 with -2b, -2x, -eom, and -neo. In both species, the fast fibers showed variable mATPase activity after preincubation at pH 9.4, and co-expressed various combinations of MyHC-2b, -2x, -2a and -eom but not -emb and -neo. MyHC-2b expressing fibers were larger and glycolytic, while MyHC-2a expressing fibers were smaller and highly oxidative in both species. To our knowledge, the present study is the first that demonstrated the expression of MyHC-2b in any of human skeletal muscles. Though the expression of MyHC genes did not correlate with the immunohistochemical profile of fibers in human MR, the expression of MyHC-2b gene was undoubtedly confirmed. CONCLUSIONS: Rat MR represent a good model that can be applied to study human MR in experiment or disease, however certain differences are to be expected due to specific oculomotor demands in humans.
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spelling pubmed-27581082009-10-07 Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles Stirn Kranjc, Branka Smerdu, Vika Eržen, Ida Graefes Arch Clin Exp Ophthalmol Medical Ophthalmology PURPOSE: To compare the organization of human and rat ocular medial recti muscles (MR). METHODS: The cryosections of human and rat MR were processed for myofibrillar ATPase (mATPase), succinate dehydrogenase and glycerol-3-phosphate dehydrogenase. To reveal myosin heavy chain (MyHC) isoforms, specific monoclonal antibodies against MyHC-1/β- slow, α-cardiac (-α), -2a, -2x, -2b, -extraocular (eom), -embryonic (-emb) and -neonatal (-neo) were applied. The MyHC gene expression was studied by in situ hybridization in human muscle. RESULTS: The muscle fibers were arranged in two distinct layers in both species. In the orbital layer most fibers were highly oxidative and expressed fast MyHC isoforms, whereas slow and oxidative fibers expressed MyHC-1 and -α, some of them also MyHC-2a, -2x, -eom, very rarely -emb, and –neo. In the global layer, slow fibers with very low oxidative and glycolytic activity and three types of fast fibers, glycolytic, oxidative and oxidative-glycolytic, could be distinguished. The slow medium-sized fibers with mATPase activity stable at pH 4.4 expressed mostly MyHC-1 and -α in rat, while in humans they co-expressed MyHC-1 with -2b, -2x, -eom, and -neo. In both species, the fast fibers showed variable mATPase activity after preincubation at pH 9.4, and co-expressed various combinations of MyHC-2b, -2x, -2a and -eom but not -emb and -neo. MyHC-2b expressing fibers were larger and glycolytic, while MyHC-2a expressing fibers were smaller and highly oxidative in both species. To our knowledge, the present study is the first that demonstrated the expression of MyHC-2b in any of human skeletal muscles. Though the expression of MyHC genes did not correlate with the immunohistochemical profile of fibers in human MR, the expression of MyHC-2b gene was undoubtedly confirmed. CONCLUSIONS: Rat MR represent a good model that can be applied to study human MR in experiment or disease, however certain differences are to be expected due to specific oculomotor demands in humans. Springer-Verlag 2009-07-17 2009-11 /pmc/articles/PMC2758108/ /pubmed/19609551 http://dx.doi.org/10.1007/s00417-009-1128-0 Text en © The Author(s) 2009
spellingShingle Medical Ophthalmology
Stirn Kranjc, Branka
Smerdu, Vika
Eržen, Ida
Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
title Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
title_full Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
title_fullStr Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
title_full_unstemmed Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
title_short Histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
title_sort histochemical and immunohistochemical profile of human and rat ocular medial rectus muscles
topic Medical Ophthalmology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758108/
https://www.ncbi.nlm.nih.gov/pubmed/19609551
http://dx.doi.org/10.1007/s00417-009-1128-0
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