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Fibroblast fusion to the muscle fiber regulates myotendinous junction formation

Vertebrate muscles and tendons are derived from distinct embryonic origins yet they must interact in order to facilitate muscle contraction and body movements. How robust muscle tendon junctions (MTJs) form to be able to withstand contraction forces is still not understood. Using techniques at a sin...

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Autores principales: Yaseen, Wesal, Kraft-Sheleg, Ortal, Zaffryar-Eilot, Shelly, Melamed, Shay, Sun, Chengyi, Millay, Douglas P., Hasson, Peleg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219707/
https://www.ncbi.nlm.nih.gov/pubmed/34158500
http://dx.doi.org/10.1038/s41467-021-24159-9
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author Yaseen, Wesal
Kraft-Sheleg, Ortal
Zaffryar-Eilot, Shelly
Melamed, Shay
Sun, Chengyi
Millay, Douglas P.
Hasson, Peleg
author_facet Yaseen, Wesal
Kraft-Sheleg, Ortal
Zaffryar-Eilot, Shelly
Melamed, Shay
Sun, Chengyi
Millay, Douglas P.
Hasson, Peleg
author_sort Yaseen, Wesal
collection PubMed
description Vertebrate muscles and tendons are derived from distinct embryonic origins yet they must interact in order to facilitate muscle contraction and body movements. How robust muscle tendon junctions (MTJs) form to be able to withstand contraction forces is still not understood. Using techniques at a single cell resolution we reexamine the classical view of distinct identities for the tissues composing the musculoskeletal system. We identify fibroblasts that have switched on a myogenic program and demonstrate these dual identity cells fuse into the developing muscle fibers along the MTJs facilitating the introduction of fibroblast-specific transcripts into the elongating myofibers. We suggest this mechanism resulting in a hybrid muscle fiber, primarily along the fiber tips, enables a smooth transition from muscle fiber characteristics towards tendon features essential for forming robust MTJs. We propose that dual characteristics of junctional cells could be a common mechanism for generating stable interactions between tissues throughout the musculoskeletal system.
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spelling pubmed-82197072021-07-09 Fibroblast fusion to the muscle fiber regulates myotendinous junction formation Yaseen, Wesal Kraft-Sheleg, Ortal Zaffryar-Eilot, Shelly Melamed, Shay Sun, Chengyi Millay, Douglas P. Hasson, Peleg Nat Commun Article Vertebrate muscles and tendons are derived from distinct embryonic origins yet they must interact in order to facilitate muscle contraction and body movements. How robust muscle tendon junctions (MTJs) form to be able to withstand contraction forces is still not understood. Using techniques at a single cell resolution we reexamine the classical view of distinct identities for the tissues composing the musculoskeletal system. We identify fibroblasts that have switched on a myogenic program and demonstrate these dual identity cells fuse into the developing muscle fibers along the MTJs facilitating the introduction of fibroblast-specific transcripts into the elongating myofibers. We suggest this mechanism resulting in a hybrid muscle fiber, primarily along the fiber tips, enables a smooth transition from muscle fiber characteristics towards tendon features essential for forming robust MTJs. We propose that dual characteristics of junctional cells could be a common mechanism for generating stable interactions between tissues throughout the musculoskeletal system. Nature Publishing Group UK 2021-06-22 /pmc/articles/PMC8219707/ /pubmed/34158500 http://dx.doi.org/10.1038/s41467-021-24159-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yaseen, Wesal
Kraft-Sheleg, Ortal
Zaffryar-Eilot, Shelly
Melamed, Shay
Sun, Chengyi
Millay, Douglas P.
Hasson, Peleg
Fibroblast fusion to the muscle fiber regulates myotendinous junction formation
title Fibroblast fusion to the muscle fiber regulates myotendinous junction formation
title_full Fibroblast fusion to the muscle fiber regulates myotendinous junction formation
title_fullStr Fibroblast fusion to the muscle fiber regulates myotendinous junction formation
title_full_unstemmed Fibroblast fusion to the muscle fiber regulates myotendinous junction formation
title_short Fibroblast fusion to the muscle fiber regulates myotendinous junction formation
title_sort fibroblast fusion to the muscle fiber regulates myotendinous junction formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8219707/
https://www.ncbi.nlm.nih.gov/pubmed/34158500
http://dx.doi.org/10.1038/s41467-021-24159-9
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