Clinical pathologies of bone fracture modelled in zebrafish

Reduced bone quality or mineral density predict susceptibility to fracture and also attenuate subsequent repair. Bone regrowth is also compromised by bacterial infection, which exacerbates fracture site inflammation. Because of the cellular complexity of fracture repair, as well as genetic and envir...

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Main Authors: Tomecka, Monika J., Ethiraj, Lalith P., Sánchez, Luis M., Roehl, Henry Hamilton, Carney, Tom J.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/142422
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1424222020-11-01T05:11:29Z Clinical pathologies of bone fracture modelled in zebrafish Tomecka, Monika J. Ethiraj, Lalith P. Sánchez, Luis M. Roehl, Henry Hamilton Carney, Tom J. Lee Kong Chian School of Medicine (LKCMedicine) Institute of Molecular and Cell Biology, A*STAR Science::Medicine Fracture Bone Reduced bone quality or mineral density predict susceptibility to fracture and also attenuate subsequent repair. Bone regrowth is also compromised by bacterial infection, which exacerbates fracture site inflammation. Because of the cellular complexity of fracture repair, as well as genetic and environmental influences, there is a need for models that permit visualisation of the fracture repair process under clinically relevant conditions. To characterise the process of fracture repair in zebrafish, we employed a crush fracture of fin rays, coupled with histological and transgenic labelling of cellular responses; the results demonstrate a strong similarity to the phased response in humans. We applied our analysis to a zebrafish model of osteogenesis imperfecta (OI), which shows reduced bone quality, spontaneous fractures and propensity for non-unions. We found deficiencies in the formation of a bone callus during fracture repair in our OI model and showed that clinically employed antiresorptive bisphosphonates can reduce spontaneous fractures in OI fish and also measurably reduce fracture callus remodelling in wild-type fish. The csf1ra mutant, which has reduced osteoclast numbers, also showed reduced callus remodelling. Exposure to excessive bisphosphonate, however, disrupted callus repair. Intriguingly, neutrophils initially colonised the fracture site, but were later completely excluded. However, when fractures were infected with Staphylococcus aureus, neutrophils were retained and compromised repair. This work elevates the zebrafish bone fracture model and indicates its utility in assessing conditions of relevance to an orthopaedic setting with medium throughput.This article has an associated First Person interview with the first author of the paper. ASTAR (Agency for Sci., Tech. and Research, S’pore) Published version 2020-06-22T03:28:13Z 2020-06-22T03:28:13Z 2019 Journal Article Tomecka, M. J., Ethiraj, L. P., Sánchez, L. M., Roehl, H. H., & Carney, T. J. (2019). Clinical pathologies of bone fracture modelled in zebrafish. Disease Models & Mechanisms, 12(9), dmm037630-. doi:10.1242/dmm.037630 1754-8403 https://hdl.handle.net/10356/142422 10.1242/dmm.037630 31383797 2-s2.0-85071786254 9 12 en Disease Models & Mechanisms © 2019 The Authors (published by The Company of Biologists Ltd). This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Medicine
Fracture
Bone
spellingShingle Science::Medicine
Fracture
Bone
Tomecka, Monika J.
Ethiraj, Lalith P.
Sánchez, Luis M.
Roehl, Henry Hamilton
Carney, Tom J.
Clinical pathologies of bone fracture modelled in zebrafish
description Reduced bone quality or mineral density predict susceptibility to fracture and also attenuate subsequent repair. Bone regrowth is also compromised by bacterial infection, which exacerbates fracture site inflammation. Because of the cellular complexity of fracture repair, as well as genetic and environmental influences, there is a need for models that permit visualisation of the fracture repair process under clinically relevant conditions. To characterise the process of fracture repair in zebrafish, we employed a crush fracture of fin rays, coupled with histological and transgenic labelling of cellular responses; the results demonstrate a strong similarity to the phased response in humans. We applied our analysis to a zebrafish model of osteogenesis imperfecta (OI), which shows reduced bone quality, spontaneous fractures and propensity for non-unions. We found deficiencies in the formation of a bone callus during fracture repair in our OI model and showed that clinically employed antiresorptive bisphosphonates can reduce spontaneous fractures in OI fish and also measurably reduce fracture callus remodelling in wild-type fish. The csf1ra mutant, which has reduced osteoclast numbers, also showed reduced callus remodelling. Exposure to excessive bisphosphonate, however, disrupted callus repair. Intriguingly, neutrophils initially colonised the fracture site, but were later completely excluded. However, when fractures were infected with Staphylococcus aureus, neutrophils were retained and compromised repair. This work elevates the zebrafish bone fracture model and indicates its utility in assessing conditions of relevance to an orthopaedic setting with medium throughput.This article has an associated First Person interview with the first author of the paper.
author2 Lee Kong Chian School of Medicine (LKCMedicine)
author_facet Lee Kong Chian School of Medicine (LKCMedicine)
Tomecka, Monika J.
Ethiraj, Lalith P.
Sánchez, Luis M.
Roehl, Henry Hamilton
Carney, Tom J.
format Article
author Tomecka, Monika J.
Ethiraj, Lalith P.
Sánchez, Luis M.
Roehl, Henry Hamilton
Carney, Tom J.
author_sort Tomecka, Monika J.
title Clinical pathologies of bone fracture modelled in zebrafish
title_short Clinical pathologies of bone fracture modelled in zebrafish
title_full Clinical pathologies of bone fracture modelled in zebrafish
title_fullStr Clinical pathologies of bone fracture modelled in zebrafish
title_full_unstemmed Clinical pathologies of bone fracture modelled in zebrafish
title_sort clinical pathologies of bone fracture modelled in zebrafish
publishDate 2020
url https://hdl.handle.net/10356/142422
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