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Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles
Vertebrate extraocular muscles (EOMs) function in eye movements. The EOMs of modern jawed vertebrates consist primarily of four recti and two oblique muscles innervated by three cranial nerves. The developmental mechanisms underlying the establishment of this complex and the evolutionarily conserved...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885385/ https://www.ncbi.nlm.nih.gov/pubmed/33588955 http://dx.doi.org/10.1186/s40851-021-00170-2 |
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author | Kuroda, Shunya Adachi, Noritaka Kusakabe, Rie Kuratani, Shigeru |
author_facet | Kuroda, Shunya Adachi, Noritaka Kusakabe, Rie Kuratani, Shigeru |
author_sort | Kuroda, Shunya |
collection | PubMed |
description | Vertebrate extraocular muscles (EOMs) function in eye movements. The EOMs of modern jawed vertebrates consist primarily of four recti and two oblique muscles innervated by three cranial nerves. The developmental mechanisms underlying the establishment of this complex and the evolutionarily conserved pattern of EOMs are unknown. Chondrichthyan early embryos develop three pairs of overt epithelial coeloms called head cavities (HCs) in the head mesoderm, and each HC is believed to differentiate into a discrete subset of EOMs. However, no direct evidence of these cell fates has been provided due to the technical difficulty of lineage tracing experiments in chondrichthyans. Here, we set up an in ovo manipulation system for embryos of the cloudy catshark Scyliorhinus torazame and labeled the epithelial cells of each HC with lipophilic fluorescent dyes. This experimental system allowed us to trace the cell lineage of EOMs with the highest degree of detail and reproducibility to date. We confirmed that the HCs are indeed primordia of EOMs but showed that the morphological pattern of shark EOMs is not solely dependent on the early pattern of the head mesoderm, which transiently appears as tripartite HCs along the simple anteroposterior axis. Moreover, we found that one of the HCs gives rise to tendon progenitor cells of the EOMs, which is an exceptional condition in our previous understanding of head muscles; the tendons associated with head muscles have generally been supposed to be derived from cranial neural crest (CNC) cells, another source of vertebrate head mesenchyme. Based on interspecies comparisons, the developmental environment is suggested to be significantly different between the two ends of the rectus muscles, and this difference is suggested to be evolutionarily conserved in jawed vertebrates. We propose that the mesenchymal interface (head mesoderm vs CNC) in the environment of developing EOM is required to determine the processes of the proximodistal axis of rectus components of EOMs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40851-021-00170-2. |
format | Online Article Text |
id | pubmed-7885385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78853852021-02-17 Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles Kuroda, Shunya Adachi, Noritaka Kusakabe, Rie Kuratani, Shigeru Zoological Lett Research Article Vertebrate extraocular muscles (EOMs) function in eye movements. The EOMs of modern jawed vertebrates consist primarily of four recti and two oblique muscles innervated by three cranial nerves. The developmental mechanisms underlying the establishment of this complex and the evolutionarily conserved pattern of EOMs are unknown. Chondrichthyan early embryos develop three pairs of overt epithelial coeloms called head cavities (HCs) in the head mesoderm, and each HC is believed to differentiate into a discrete subset of EOMs. However, no direct evidence of these cell fates has been provided due to the technical difficulty of lineage tracing experiments in chondrichthyans. Here, we set up an in ovo manipulation system for embryos of the cloudy catshark Scyliorhinus torazame and labeled the epithelial cells of each HC with lipophilic fluorescent dyes. This experimental system allowed us to trace the cell lineage of EOMs with the highest degree of detail and reproducibility to date. We confirmed that the HCs are indeed primordia of EOMs but showed that the morphological pattern of shark EOMs is not solely dependent on the early pattern of the head mesoderm, which transiently appears as tripartite HCs along the simple anteroposterior axis. Moreover, we found that one of the HCs gives rise to tendon progenitor cells of the EOMs, which is an exceptional condition in our previous understanding of head muscles; the tendons associated with head muscles have generally been supposed to be derived from cranial neural crest (CNC) cells, another source of vertebrate head mesenchyme. Based on interspecies comparisons, the developmental environment is suggested to be significantly different between the two ends of the rectus muscles, and this difference is suggested to be evolutionarily conserved in jawed vertebrates. We propose that the mesenchymal interface (head mesoderm vs CNC) in the environment of developing EOM is required to determine the processes of the proximodistal axis of rectus components of EOMs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40851-021-00170-2. BioMed Central 2021-02-15 /pmc/articles/PMC7885385/ /pubmed/33588955 http://dx.doi.org/10.1186/s40851-021-00170-2 Text en © The Author(s) 2021 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 | Research Article Kuroda, Shunya Adachi, Noritaka Kusakabe, Rie Kuratani, Shigeru Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
title | Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
title_full | Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
title_fullStr | Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
title_full_unstemmed | Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
title_short | Developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
title_sort | developmental fates of shark head cavities reveal mesodermal contributions to tendon progenitor cells in extraocular muscles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7885385/ https://www.ncbi.nlm.nih.gov/pubmed/33588955 http://dx.doi.org/10.1186/s40851-021-00170-2 |
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