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Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear

The middle ear muscles have vital roles, yet their precise function in hearing and protection remains unclear. To better understand the function of these muscles in humans, the morphology, fiber composition, and metabolic properties of nine tensor tympani and eight stapedius muscles were analyzed wi...

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Autores principales: Rönnblom, Anton, Thornell, Lars‐Eric, Shah, Farhan, Tano, Krister, Stål, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273355/
https://www.ncbi.nlm.nih.gov/pubmed/36914412
http://dx.doi.org/10.1111/joa.13861
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author Rönnblom, Anton
Thornell, Lars‐Eric
Shah, Farhan
Tano, Krister
Stål, Per
author_facet Rönnblom, Anton
Thornell, Lars‐Eric
Shah, Farhan
Tano, Krister
Stål, Per
author_sort Rönnblom, Anton
collection PubMed
description The middle ear muscles have vital roles, yet their precise function in hearing and protection remains unclear. To better understand the function of these muscles in humans, the morphology, fiber composition, and metabolic properties of nine tensor tympani and eight stapedius muscles were analyzed with immunohistochemical, enzyme‐histochemical, biochemical, and morphometric techniques. Human orofacial, jaw, extraocular, and limb muscles were used as references. The immunohistochemical analysis showed that the stapedius and tensor tympani muscles were markedly dominated by fibers expressing fast contracting myosin heavy chain MyHC‐2A and MyHC‐2X (79 ± 6% vs. 86 ± 9%, respectively, p = 0.04). In fact, the middle ear muscles had one of the highest proportions of MyHC‐2 fibers ever reported for human muscles. Interestingly, the biochemical analysis revealed a MyHC isoform of unknown identity in both the stapedius and tensor tympani muscles. Muscle fibers containing two or more MyHC isoforms were relatively frequently observed in both muscles. A proportion of these hybrid fibers expressed a developmental MyHC isoform that is normally absent in adult human limb muscles. The middle ear muscles differed from orofacial, jaw, and limb muscles by having significantly smaller fibers (220 vs. 360 μm(2), respectively) and significantly higher variability in fiber size, capillarization per fiber area, mitochondrial oxidative activity, and density of nerve fascicles. Muscle spindles were observed in the tensor tympani muscle but not in the stapedius muscle. We conclude that the middle ear muscles have a highly specialized muscle morphology, fiber composition, and metabolic properties that generally showed more similarities to orofacial than jaw and limb muscles. Although the muscle fiber characteristics in the tensor tympani and stapedius muscles suggest a capacity for fast, fine‐tuned, and sustainable contractions, their difference in proprioceptive control reflects different functions in hearing and protection of the inner ear.
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spelling pubmed-102733552023-06-17 Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear Rönnblom, Anton Thornell, Lars‐Eric Shah, Farhan Tano, Krister Stål, Per J Anat Original Articles The middle ear muscles have vital roles, yet their precise function in hearing and protection remains unclear. To better understand the function of these muscles in humans, the morphology, fiber composition, and metabolic properties of nine tensor tympani and eight stapedius muscles were analyzed with immunohistochemical, enzyme‐histochemical, biochemical, and morphometric techniques. Human orofacial, jaw, extraocular, and limb muscles were used as references. The immunohistochemical analysis showed that the stapedius and tensor tympani muscles were markedly dominated by fibers expressing fast contracting myosin heavy chain MyHC‐2A and MyHC‐2X (79 ± 6% vs. 86 ± 9%, respectively, p = 0.04). In fact, the middle ear muscles had one of the highest proportions of MyHC‐2 fibers ever reported for human muscles. Interestingly, the biochemical analysis revealed a MyHC isoform of unknown identity in both the stapedius and tensor tympani muscles. Muscle fibers containing two or more MyHC isoforms were relatively frequently observed in both muscles. A proportion of these hybrid fibers expressed a developmental MyHC isoform that is normally absent in adult human limb muscles. The middle ear muscles differed from orofacial, jaw, and limb muscles by having significantly smaller fibers (220 vs. 360 μm(2), respectively) and significantly higher variability in fiber size, capillarization per fiber area, mitochondrial oxidative activity, and density of nerve fascicles. Muscle spindles were observed in the tensor tympani muscle but not in the stapedius muscle. We conclude that the middle ear muscles have a highly specialized muscle morphology, fiber composition, and metabolic properties that generally showed more similarities to orofacial than jaw and limb muscles. Although the muscle fiber characteristics in the tensor tympani and stapedius muscles suggest a capacity for fast, fine‐tuned, and sustainable contractions, their difference in proprioceptive control reflects different functions in hearing and protection of the inner ear. John Wiley and Sons Inc. 2023-03-13 /pmc/articles/PMC10273355/ /pubmed/36914412 http://dx.doi.org/10.1111/joa.13861 Text en © 2023 The Authors. Journal of Anatomy published by John Wiley & Sons Ltd on behalf of Anatomical Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Rönnblom, Anton
Thornell, Lars‐Eric
Shah, Farhan
Tano, Krister
Stål, Per
Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
title Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
title_full Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
title_fullStr Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
title_full_unstemmed Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
title_short Unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
title_sort unique fiber phenotype composition and metabolic properties of the stapedius and tensor tympani muscles in the human middle ear
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273355/
https://www.ncbi.nlm.nih.gov/pubmed/36914412
http://dx.doi.org/10.1111/joa.13861
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