Zebrafish as an Emerging Model for Osteoporosis: A Primary Testing Platform for Screening New Osteo-Active Compounds

被引:115
作者
Bergen, Dylan J. M. [1 ,2 ]
Kague, Erika [1 ]
Hammond, Chrissy L. [1 ]
机构
[1] Univ Bristol, Sch Physiol Pharmacol & Neurosci, Biomed Sci Bldg, Bristol, Avon, England
[2] Univ Bristol, Musculoskeletal Res Unit, Translat Hlth Sci, Bristol Med Sch,Southmead Hosp, Bristol, Avon, England
基金
英国惠康基金;
关键词
zebrafish; screening; genetic mutants; osteoblast; osteoclast; osteoporosis; drug development; animal model; DANIO-RERIO; INDUCED INHIBITION; BONE METABOLISM; RETINOIC ACID; OSTEOGENESIS; GENE; MUTATIONS; PROTEIN; GENOME; COLLAGEN;
D O I
10.3389/fendo.2019.00006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 aging 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.
引用
收藏
页数:20
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共 165 条
[51]   Two pioneering osteoporosis drugs finally approach approval [J].
Garber, Ken .
NATURE REVIEWS DRUG DISCOVERY, 2016, 15 (07) :445-446
[52]   Immune Suppressive and Bone Inhibitory Effects of Prednisolone in Growing and Regenerating Zebrafish Tissues [J].
Geurtzen, Karina ;
Vernet, Aude ;
Freidin, Andrew ;
Rauner, Martina ;
Hofbauer, Lorenz C. ;
Schneider, Jurgen E. ;
Brand, Michael ;
Knopf, Franziska .
JOURNAL OF BONE AND MINERAL RESEARCH, 2017, 32 (12) :2476-2488
[53]   The chaperone activity of 4PBA ameliorates the skeletal phenotype of Chihuahua, a zebrafish model for dominant osteogenesis imperfecta [J].
Gioia, Roberta ;
Tonelli, Francesca ;
Ceppi, Ilaria ;
Biggiogera, Marco ;
Leikin, Sergey ;
Fisher, Shannon ;
Tenedini, Elena ;
Yorgan, Timur A. ;
Schinke, Thorsten ;
Tian, Kun ;
Schwartz, Jean-Marc ;
Forte, Fabiana ;
Wagener, Raimund ;
Villani, Simona ;
Rossi, Antonio ;
Forlino, Antonella .
HUMAN MOLECULAR GENETICS, 2017, 26 (15) :2897-2911
[54]   Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin [J].
Gistelinck, C. ;
Gioia, R. ;
Gagliardi, A. ;
Tonelli, F. ;
Marchese, L. ;
Bianchi, L. ;
Landi, C. ;
Bini, L. ;
Huysseune, A. ;
Witten, P. E. ;
Staes, A. ;
Gevaert, K. ;
De Rocker, N. ;
Menten, B. ;
Malfait, F. ;
Leikin, S. ;
Carra, S. ;
Tenni, R. ;
Rossi, A. ;
De Paepe, A. ;
Coucke, P. ;
Willaert, A. ;
Forlino, A. .
SCIENTIFIC REPORTS, 2016, 6
[55]   Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies [J].
Gistelinck, Charlotte ;
Kwon, Ronald Y. ;
Malfait, Fransiska ;
Symoens, Sofie ;
Harris, Matthew P. ;
Henke, Katrin ;
Hawkins, Michael B. ;
Fisher, Shannon ;
Sips, Patrick ;
Guillemyn, Brecht ;
Bek, Jan Willem ;
Vermassen, Petra ;
De Saffel, Hanna ;
Witten, Paul Eckhard ;
Weis, MaryAnn ;
De Paepe, Anne ;
Eyre, David R. ;
Willaert, Andy ;
Coucke, Paul J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (34) :E8037-E8046
[56]   A gain of function mutation causing skeletal overgrowth in the rapunzel mutant [J].
Green, Julie ;
Taylor, Jennifer J. ;
Hindes, Anna ;
Johnson, Stephen L. ;
Goldsmith, Matthew I. .
DEVELOPMENTAL BIOLOGY, 2009, 334 (01) :224-234
[57]   'Sink or swim': an evaluation of the clinical characteristics of individuals with high bone mass [J].
Gregson, C. L. ;
Steel, S. A. ;
O'Rourke, K. P. ;
Allan, K. ;
Ayuk, J. ;
Bhalla, A. ;
Clunie, G. ;
Crabtree, N. ;
Fogelman, I. ;
Goodby, A. ;
Langman, C. M. ;
Linton, S. ;
Marriott, E. ;
McCloskey, E. ;
Moss, K. E. ;
Palferman, T. ;
Panthakalam, S. ;
Poole, K. E. S. ;
Stone, M. D. ;
Turton, J. ;
Wallis, D. ;
Warburton, S. ;
Wass, J. ;
Duncan, E. L. ;
Brown, M. A. ;
Davey-Smith, G. ;
Tobias, J. H. .
OSTEOPOROSIS INTERNATIONAL, 2012, 23 (02) :643-654
[58]   Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes [J].
Gregson, Celia L. ;
Newell, Felicity ;
Leo, Paul J. ;
Clark, Graeme R. ;
Paternoster, Lavinia ;
Marshall, Mhairi ;
Forgetta, Vincenzo ;
Morris, John A. ;
Ge, Bing ;
Bao, Xiao ;
Bassett, J. H. Duncan ;
Williams, Graham R. ;
Youlten, Scott E. ;
Croucher, Peter I. ;
Smith, George Davey ;
Evans, David M. ;
Kemp, John P. ;
Brown, Matthew A. ;
Tobias, Jon H. ;
Duncan, Emma L. .
BONE, 2018, 114 :62-71
[59]   Mutations in Known Monogenic High Bone Mass Loci Only Explain a Small Proportion of High Bone Mass Cases [J].
Gregson, Celia L. ;
Wheeler, Lawrie ;
Hardcastle, Sarah A. ;
Appleton, Louise H. ;
Addison, Kathryn A. ;
Brugmans, Marieke ;
Clark, Graeme R. ;
Ward, Kate A. ;
Paggiosi, Margaret ;
Stone, Mike ;
Thomas, Joegi ;
Agarwal, Rohan ;
Poole, Kenneth E. S. ;
McCloskey, Eugene ;
Fraser, William D. ;
Williams, Eleanor ;
Bullock, Alex N. ;
Davey Smith, George ;
Brown, Matthew A. ;
Tobias, Jon H. ;
Duncan, Emma L. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2016, 31 (03) :640-649
[60]  
Haffter P, 1996, DEVELOPMENT, V123, P1