Zebrafish development and regeneration: new tools for biomedical research

被引:133
作者
Brittijn, Sebastiaan A. [1 ]
Duivesteijn, Suzanne J. [1 ]
Belmamoune, Mounia [2 ]
Bertens, Laura F. M. [2 ]
Bitter, Wilbert [3 ]
De Bruijn, Joost D. [4 ,5 ]
Champagne, Danielle L. [6 ]
Cuppen, Edwin [7 ]
Flik, Gert [8 ]
Vandenbroucke-Grauls, Christina M. [3 ]
Janssen, Richard A. J. [9 ]
De Jong, Ilse M. L. [1 ]
De Kloet, Edo Ronald [6 ]
Kros, Alexander [10 ]
Meijer, Annemarie H. [11 ]
Metz, Juriaan R. [8 ]
Van Der Sar, Astrid M. [3 ]
Schaaf, Marcel J. M. [1 ,11 ]
Schulte-Merker, Stefan [7 ]
Spaink, Herman P. [11 ,12 ]
Tak, Paul P. [13 ]
Verbeek, Fons J. [2 ]
Vervoordeldonk, Margriet J. [14 ]
Vonk, Freek J. [1 ]
Witte, Frans [1 ]
Yuan, Huipin [4 ]
Richardson, Michael K. [1 ]
机构
[1] Leiden Univ, Inst Biol, Dept Integrat Zool, NL-2311 GP Leiden, Netherlands
[2] Leiden Univ, Leiden Inst Adv Comp Sci, NL-2311 GP Leiden, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Dept Med Microbiol & Infect Control, Amsterdam, Netherlands
[4] MB Bilthoven, Progentix BV, Bilthoven, Netherlands
[5] Queen Mary Univ London, Sch Mat Sci & Engn, London, England
[6] Leiden Univ, Med Ctr, NL-2311 GP Leiden, Netherlands
[7] Hubrecht Inst, Utrecht, Netherlands
[8] Radboud Univ Nijmegen, Inst Water & Wetland Res, Dept Organismal Anim Physiol, Nijmegen, Netherlands
[9] BioFocusDPI, Leiden, Netherlands
[10] Leiden Univ, Gorlaeus Labs, Leiden Inst Chem, NL-2311 GP Leiden, Netherlands
[11] Leiden Univ, Dept Mol Cell Biol, Inst Biol, NL-2311 GP Leiden, Netherlands
[12] ZFscreens, Leiden, Netherlands
[13] Univ Amsterdam, Acad Med Ctr, Div Clin Immunol & Rheumatol, NL-1012 WX Amsterdam, Netherlands
[14] Arthrogen BV, Amsterdam, Netherlands
关键词
Danio rerio; zebrafish; high-throughput screening; high-content screening; CALCIUM-PHOSPHATE BCP; IN-VIVO; RETINOIC ACID; LIMB REGENERATION; BONE-FORMATION; MODEL SYSTEM; GRANULOMA-FORMATION; FIN REGENERATION; DRUG DISCOVERY; ANIMAL-MODELS;
D O I
10.1387/ijdb.082615sb
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Basic research in pattern formation is concerned with the generation of phenotypes and tissues. It can therefore lead to new tools for medical research. These include phenotypic screening assays, applications in tissue engineering, as well as general advances in biomedical knowledge. Our aim here is to discuss this emerging field with special reference to tools based on zebrafish developmental biology. We describe phenotypic screening assays being developed in our own and other labs. Our assays involve: (i) systemic or local administration of a test compound or drug to zebrafish in vivo, (ii) the subsequent detection or "readout" of a defined phenotypic change. A positive readout may result from binding of the test compound to a molecular target involved in a developmental pathway. We present preliminary data on assays for compounds that modulate skeletal patterning, bone turnover, immune responses, inflammation and early-life stress. The assays use live zebrafish embryos and larvae as well as adult fish undergoing caudal fin regeneration. We describe proof-of-concept studies on the localised targeting of compounds into regeneration blastemas using microcarriers. Zebrafish are cheaper to maintain than rodents, produce large numbers of transparent eggs, and some zebrafish assays could be scaled-up into medium and high throughput screens. However, advances in automation and imaging are required. Zebrafish cannot replace mammalian models in the drug development pipeline. Nevertheless, they can provide a cost-effective bridge between cell-based assays and mammalian whole-organism models.
引用
收藏
页码:835 / 850
页数:16
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