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Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening

BACKGROUND: The zebrafish (Danio rerio) has recently been shown to be an ideal model to study bone disease including osteoporosis. The zebrafish osteoporosis model could be induced by glucocorticoid treatment with chemical staining for reflecting the level of bone mineralization. However, this metho...

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Autores principales: Huang, Hong‐xin, Lin, Hao, Lan, Fen, Wu, Yong‐fu, Yang, Zhen‐guo, Zhang, Jing‐jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354313/
https://www.ncbi.nlm.nih.gov/pubmed/30891547
http://dx.doi.org/10.1002/ame2.12000
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author Huang, Hong‐xin
Lin, Hao
Lan, Fen
Wu, Yong‐fu
Yang, Zhen‐guo
Zhang, Jing‐jing
author_facet Huang, Hong‐xin
Lin, Hao
Lan, Fen
Wu, Yong‐fu
Yang, Zhen‐guo
Zhang, Jing‐jing
author_sort Huang, Hong‐xin
collection PubMed
description BACKGROUND: The zebrafish (Danio rerio) has recently been shown to be an ideal model to study bone disease including osteoporosis. The zebrafish osteoporosis model could be induced by glucocorticoid treatment with chemical staining for reflecting the level of bone mineralization. However, this methodology was unstable. Here, we developed a novel methodology to directly evaluate the bone mass and density. METHODS: We generated and used the bone of transgenic zebrafish Tg (ola.sp7:nlsGFP) to evaluate the bone mass and density by measuring the areal extent and the integrated optical density (IOD) of enhanced green fluorescent protein (eGFP). This methodology was further compared with the traditional chemically stained method showing the bone mineralization. Furthermore, genes related to zebrafish osteoporosis were analyzed by quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR). RESULTS: Our results of new methods were consistent with those from chemically stained fish, following glucocorticoid‐induction or epimedium flavonoid (FE)‐rescue treatments. qRT‐PCR analyses on mRNA levels revealed that glucocorticoid induces osteoporosis by downregulating the expression of osteoblast‐related factors osterix, osteocalcin, and osteopontin, and upregulating the expression of osteoclast‐related factor tartrate‐resistant acid phosphatase. In FE‐rescued fish, the expression of osteogenic factors osterix, osteocalcin, and osteopontin were increased. CONCLUSION: Compared to the traditional chemical staining methods, the new osteoporosis model using Tg(ola.sp7:nlsGFP) is more convenient and efficient for studying osteoporosis in vivo, and especially for high‐throughput anti‐osteoporosis drug screening.
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spelling pubmed-63543132019-03-19 Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening Huang, Hong‐xin Lin, Hao Lan, Fen Wu, Yong‐fu Yang, Zhen‐guo Zhang, Jing‐jing Animal Model Exp Med Original Articles BACKGROUND: The zebrafish (Danio rerio) has recently been shown to be an ideal model to study bone disease including osteoporosis. The zebrafish osteoporosis model could be induced by glucocorticoid treatment with chemical staining for reflecting the level of bone mineralization. However, this methodology was unstable. Here, we developed a novel methodology to directly evaluate the bone mass and density. METHODS: We generated and used the bone of transgenic zebrafish Tg (ola.sp7:nlsGFP) to evaluate the bone mass and density by measuring the areal extent and the integrated optical density (IOD) of enhanced green fluorescent protein (eGFP). This methodology was further compared with the traditional chemically stained method showing the bone mineralization. Furthermore, genes related to zebrafish osteoporosis were analyzed by quantitative reverse transcription‐polymerase chain reaction (qRT‐PCR). RESULTS: Our results of new methods were consistent with those from chemically stained fish, following glucocorticoid‐induction or epimedium flavonoid (FE)‐rescue treatments. qRT‐PCR analyses on mRNA levels revealed that glucocorticoid induces osteoporosis by downregulating the expression of osteoblast‐related factors osterix, osteocalcin, and osteopontin, and upregulating the expression of osteoclast‐related factor tartrate‐resistant acid phosphatase. In FE‐rescued fish, the expression of osteogenic factors osterix, osteocalcin, and osteopontin were increased. CONCLUSION: Compared to the traditional chemical staining methods, the new osteoporosis model using Tg(ola.sp7:nlsGFP) is more convenient and efficient for studying osteoporosis in vivo, and especially for high‐throughput anti‐osteoporosis drug screening. John Wiley and Sons Inc. 2018-04-19 /pmc/articles/PMC6354313/ /pubmed/30891547 http://dx.doi.org/10.1002/ame2.12000 Text en © 2018 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Huang, Hong‐xin
Lin, Hao
Lan, Fen
Wu, Yong‐fu
Yang, Zhen‐guo
Zhang, Jing‐jing
Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
title Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
title_full Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
title_fullStr Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
title_full_unstemmed Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
title_short Application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
title_sort application of bone transgenic zebrafish in anti‐osteoporosis chemical screening
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354313/
https://www.ncbi.nlm.nih.gov/pubmed/30891547
http://dx.doi.org/10.1002/ame2.12000
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