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Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull

Efforts to understand the morphogenesis of complex craniofacial structures have largely focused on the role of chondrocytes and osteoblasts. Along with these bone–creating cells, bone–resorbing osteoclasts are critical in homeostasis of adult skeletal structures, but there is currently limited infor...

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Autores principales: Miao, Kelly Z., Cozzone, Austin, Caetano-Lopes, Joana, Harris, Matthew P., Fisher, Shannon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664155/
https://www.ncbi.nlm.nih.gov/pubmed/36387889
http://dx.doi.org/10.3389/fendo.2022.969481
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author Miao, Kelly Z.
Cozzone, Austin
Caetano-Lopes, Joana
Harris, Matthew P.
Fisher, Shannon
author_facet Miao, Kelly Z.
Cozzone, Austin
Caetano-Lopes, Joana
Harris, Matthew P.
Fisher, Shannon
author_sort Miao, Kelly Z.
collection PubMed
description Efforts to understand the morphogenesis of complex craniofacial structures have largely focused on the role of chondrocytes and osteoblasts. Along with these bone–creating cells, bone–resorbing osteoclasts are critical in homeostasis of adult skeletal structures, but there is currently limited information on their role in the complex morphogenetic events of craniofacial development. Fundamental aspects of skull formation and general skeletal development are conserved from zebrafish to mammals. Using a cathepsinK reporter, we documented osteoclast location in the developing zebrafish skull over several weeks, from 5.18 mm to 9.6 mm standard length (approximately 15 to 34 days post fertilization). While broad distribution of osteoclasts is consistent across individuals, they are sparse and the exact locations vary among fish and across developmental time points. Interestingly, we observed osteoclasts concentrating at areas associated with neuromasts and their associated nerves, in particular the hyomandibular foramina and around the supraorbital lateral line. These are areas of active remodeling. In contrast, other areas of rapid bone growth, such as the osteogenic fronts of the frontal and parietal bones, show no particular concentration of osteoclasts, suggesting that they play a special role in shaping bone near neuromasts and nerves. In csf1ra mutants lacking functional osteoclasts, the morphology of the cranial bone was disrupted in both areas. The hyomandibular foramen is present in the initial cartilage template, but after the initiation of ossification, the diameter of the canal is significantly smaller in the absence of osteoclasts. The diameter of the supraorbital lateral line canals was also reduced in the mutants, as was the number of pores associated with neuromasts, which allow for the passage of associated nerves through the bone. Our findings define important and previously unappreciated roles for osteoclast activity in shaping craniofacial skeletal structures with a particular role in bone modeling around peripheral cranial nerves, providing a scaffold for wiring the sensioneural system during craniofacial development. This has important implications for the formation of the evolutionarily diverse lateral line system, as well understanding the mechanism of neurologic sequelae of congenital osteoclast dysfunction in human craniofacial development.
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spelling pubmed-96641552022-11-15 Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull Miao, Kelly Z. Cozzone, Austin Caetano-Lopes, Joana Harris, Matthew P. Fisher, Shannon Front Endocrinol (Lausanne) Endocrinology Efforts to understand the morphogenesis of complex craniofacial structures have largely focused on the role of chondrocytes and osteoblasts. Along with these bone–creating cells, bone–resorbing osteoclasts are critical in homeostasis of adult skeletal structures, but there is currently limited information on their role in the complex morphogenetic events of craniofacial development. Fundamental aspects of skull formation and general skeletal development are conserved from zebrafish to mammals. Using a cathepsinK reporter, we documented osteoclast location in the developing zebrafish skull over several weeks, from 5.18 mm to 9.6 mm standard length (approximately 15 to 34 days post fertilization). While broad distribution of osteoclasts is consistent across individuals, they are sparse and the exact locations vary among fish and across developmental time points. Interestingly, we observed osteoclasts concentrating at areas associated with neuromasts and their associated nerves, in particular the hyomandibular foramina and around the supraorbital lateral line. These are areas of active remodeling. In contrast, other areas of rapid bone growth, such as the osteogenic fronts of the frontal and parietal bones, show no particular concentration of osteoclasts, suggesting that they play a special role in shaping bone near neuromasts and nerves. In csf1ra mutants lacking functional osteoclasts, the morphology of the cranial bone was disrupted in both areas. The hyomandibular foramen is present in the initial cartilage template, but after the initiation of ossification, the diameter of the canal is significantly smaller in the absence of osteoclasts. The diameter of the supraorbital lateral line canals was also reduced in the mutants, as was the number of pores associated with neuromasts, which allow for the passage of associated nerves through the bone. Our findings define important and previously unappreciated roles for osteoclast activity in shaping craniofacial skeletal structures with a particular role in bone modeling around peripheral cranial nerves, providing a scaffold for wiring the sensioneural system during craniofacial development. This has important implications for the formation of the evolutionarily diverse lateral line system, as well understanding the mechanism of neurologic sequelae of congenital osteoclast dysfunction in human craniofacial development. Frontiers Media S.A. 2022-11-01 /pmc/articles/PMC9664155/ /pubmed/36387889 http://dx.doi.org/10.3389/fendo.2022.969481 Text en Copyright © 2022 Miao, Cozzone, Caetano-Lopes, Harris and Fisher https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Miao, Kelly Z.
Cozzone, Austin
Caetano-Lopes, Joana
Harris, Matthew P.
Fisher, Shannon
Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
title Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
title_full Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
title_fullStr Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
title_full_unstemmed Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
title_short Osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
title_sort osteoclast activity sculpts craniofacial form to permit sensorineural patterning in the zebrafish skull
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9664155/
https://www.ncbi.nlm.nih.gov/pubmed/36387889
http://dx.doi.org/10.3389/fendo.2022.969481
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