Abstract
Osteoporosis is metabolic bone disease caused by an altered balance between bone anabolism and catabolism. This dysregulated balance is responsible for fragile bones that fracture easily after minor falls. With an ageing population, the incidence is rising and as yet pharmaceutical options to restore this imbalance is limited, especially stimulating osteoblast bone-building activity. Excitingly, output from large genetic studies on people with high bone mass (HBM) cases and genome wide association studies (GWAS) on the population, yielded new insights into pathways containing osteo-anabolic players that have potential for drug target development. However, a bottleneck in development of new treatments targeting these putative osteo-anabolic genes is the lack of animal models for rapid and affordable testing to generate functional data and that simultaneously can be used as a compound testing platform. Zebrafish, a small teleost fish, are increasingly used in functional genomics and drug screening assays which resulted in new treatments in the clinic for other diseases. In this review we outline the zebrafish as a powerful model for osteoporosis research to validate potential therapeutic candidates, describe the tools and assays that can be used to study bone homeostasis, and affordable (semi-)high-throughput compound testing.
| Original language | English |
|---|---|
| Article number | 6 |
| Number of pages | 20 |
| Journal | Frontiers in Endocrinology |
| Volume | 10 |
| Issue number | JAN |
| DOIs | |
| Publication status | Published - 29 Jan 2019 |
Keywords
- Zebrafish
- screening
- genetic mutants
- osteo blast
- osteoporosis
- drug development
- animal model
- osteoblast
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Dive into the research topics of 'Zebrafish as an emerging model for osteoporosis: a primary testing platform for screening new osteo-active compounds'. Together they form a unique fingerprint.Research output
- 128 Citations
- 2 Article (Academic Journal)
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Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease
Bergen, D. J. M., Tong, Q., Shukla, A., Newham, E., Zethof, J., Lundberg, M., Ryan, R., Youlten, S. E., Frysz, M., Croucher, P. I., Flik, G., Richardson, R. J., Kemp, J. P., Hammond, C. L. & Metz, J. R., 21 Jan 2022, In: BMC Biology. 20, 1, 25 p., 21.Research output: Contribution to journal › Article (Academic Journal) › peer-review
Open AccessFile30 Citations (Scopus)176 Downloads (Pure) -
Pharmacological Manipulation of Early Zebrafish Skeletal Development Shows an Important Role for Smad9 in Control of Skeletal Progenitor Populations
McDonald, G. L. K., Wang, M., Hammond, C. L. & Bergen, D. J. M., 13 Feb 2021, (E-pub ahead of print) In: Biomolecules. 11, 2, p. 1-20 20 p., 277.Research output: Contribution to journal › Article (Academic Journal) › peer-review
Open AccessFile4 Citations (Scopus)136 Downloads (Pure)
Projects
- 2 Active
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Functional validation of novel osteo-anabolic factors in the zebrafish
Bergen, D. J. M. (Principal Investigator)
1/04/19 → …
Project: Research
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In silico prioritisation of genes that underpin osteoporosis
Bergen, D. J. M. (Principal Investigator)
1/09/17 → …
Project: Research
Prizes
Activities
- 1 Fellowship awarded competitively
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Discipline Hopping fellowship, title: 'In silico prioritisation and validation of causal genes that underpin osteoporosis pathogenesis'
Bergen, D. J. M. (Recipient)
17 Jun 2017Activity: Other activity types › Fellowship awarded competitively
Equipment
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