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Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue

BACKGROUND: The arrangement of myonuclei in skeletal muscle tissue has long been used as a biomarker for muscle health, but there is a dearth of in vivo exploration of potential effects of myonuclear organization on the function and regeneration of skeletal muscle because traditional nuclear stains...

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Autores principales: Hastings, Robert Louis, Massopust, Ryan T., Haddix, Seth G., Lee, Young il, Thompson, Wesley J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204059/
https://www.ncbi.nlm.nih.gov/pubmed/32381068
http://dx.doi.org/10.1186/s13395-020-00233-6
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author Hastings, Robert Louis
Massopust, Ryan T.
Haddix, Seth G.
Lee, Young il
Thompson, Wesley J.
author_facet Hastings, Robert Louis
Massopust, Ryan T.
Haddix, Seth G.
Lee, Young il
Thompson, Wesley J.
author_sort Hastings, Robert Louis
collection PubMed
description BACKGROUND: The arrangement of myonuclei in skeletal muscle tissue has long been used as a biomarker for muscle health, but there is a dearth of in vivo exploration of potential effects of myonuclear organization on the function and regeneration of skeletal muscle because traditional nuclear stains are performed on postmortem tissue. Therefore, we sought a transgenic method to produce a selective and persistent myonuclear label in whole muscles of living mice. METHODS: We bred together a mouse line with skeletal muscle fiber-selective expression of Cre recombinase and a second mouse line with a Cre-inducible fluorescently tagged histone protein to generate a mouse line that produces a myonuclear label suitable for vital imaging and histology of fixed tissue. We tested the effectiveness of this vital label in three conditions known to generate abnormal myonuclear positioning. First, we injured myofibers of young mice with cardiotoxin. Second, this nuclear label was bred into a murine model of Duchenne muscular dystrophy. Finally, we examined old mice from this line that have undergone the natural aging process. Welch’s t test was used to compare wild type and transgenic mice. RESULTS: The resulting mouse line transgenically produces a vital red fluorescent label of myonuclei, which facilitates their in vivo imaging in skeletal muscle tissue. Transgenic fluorescent labeling of myonuclei has no significant effect on skeletal muscle function, as determined by twitch and tetanic force recordings. In each muscle examined, including those under damaged, dystrophic, and aged conditions, the labeled myonuclei exhibit morphology consistent with established literature, and reveal a specialized arrangement of subsynaptic myonuclei at the neuromuscular junction. CONCLUSIONS: Taken together, our results demonstrate that this mouse line provides a versatile tool to selectively visualize myonuclei within both living and fixed preparations of healthy, injured, diseased, and aged muscles.
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spelling pubmed-72040592020-05-12 Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue Hastings, Robert Louis Massopust, Ryan T. Haddix, Seth G. Lee, Young il Thompson, Wesley J. Skelet Muscle Methodology BACKGROUND: The arrangement of myonuclei in skeletal muscle tissue has long been used as a biomarker for muscle health, but there is a dearth of in vivo exploration of potential effects of myonuclear organization on the function and regeneration of skeletal muscle because traditional nuclear stains are performed on postmortem tissue. Therefore, we sought a transgenic method to produce a selective and persistent myonuclear label in whole muscles of living mice. METHODS: We bred together a mouse line with skeletal muscle fiber-selective expression of Cre recombinase and a second mouse line with a Cre-inducible fluorescently tagged histone protein to generate a mouse line that produces a myonuclear label suitable for vital imaging and histology of fixed tissue. We tested the effectiveness of this vital label in three conditions known to generate abnormal myonuclear positioning. First, we injured myofibers of young mice with cardiotoxin. Second, this nuclear label was bred into a murine model of Duchenne muscular dystrophy. Finally, we examined old mice from this line that have undergone the natural aging process. Welch’s t test was used to compare wild type and transgenic mice. RESULTS: The resulting mouse line transgenically produces a vital red fluorescent label of myonuclei, which facilitates their in vivo imaging in skeletal muscle tissue. Transgenic fluorescent labeling of myonuclei has no significant effect on skeletal muscle function, as determined by twitch and tetanic force recordings. In each muscle examined, including those under damaged, dystrophic, and aged conditions, the labeled myonuclei exhibit morphology consistent with established literature, and reveal a specialized arrangement of subsynaptic myonuclei at the neuromuscular junction. CONCLUSIONS: Taken together, our results demonstrate that this mouse line provides a versatile tool to selectively visualize myonuclei within both living and fixed preparations of healthy, injured, diseased, and aged muscles. BioMed Central 2020-05-07 /pmc/articles/PMC7204059/ /pubmed/32381068 http://dx.doi.org/10.1186/s13395-020-00233-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Hastings, Robert Louis
Massopust, Ryan T.
Haddix, Seth G.
Lee, Young il
Thompson, Wesley J.
Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
title Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
title_full Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
title_fullStr Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
title_full_unstemmed Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
title_short Exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
title_sort exclusive vital labeling of myonuclei for studying myonuclear arrangement in mouse skeletal muscle tissue
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7204059/
https://www.ncbi.nlm.nih.gov/pubmed/32381068
http://dx.doi.org/10.1186/s13395-020-00233-6
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