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斑马鱼的发育与再生:生物医学研究的新工具

Zebrafish development and regeneration: new tools for biomedical research.

作者信息

Brittijn Sebastiaan A, Duivesteijn Suzanne J, Belmamoune Mounia, Bertens Laura F M, Bitter Wilbert, de Bruijn Joost D, Champagne Danielle L, Cuppen Edwin, Flik Gert, Vandenbroucke-Grauls Christina M, Janssen Richard A J, de Jong Ilse M L, de Kloet Edo Ronald, Kros Alexander, Meijer Annemarie H, Metz Juriaan R, van der Sar Astrid M, Schaaf Marcel J M, Schulte-Merker Stefan, Spaink Herman P, Tak Paul P, Verbeek Fons J, Vervoordeldonk Margriet J, Vonk Freek J, Witte Frans, Yuan Huipin, Richardson Michael K

机构信息

Institute of Biology, Dept. Integrative Zoology, University of Leiden, The Netherlands.

出版信息

Int J Dev Biol. 2009;53(5-6):835-50. doi: 10.1387/ijdb.082615sb.

Abstract

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.

摘要

模式形成的基础研究关注表型和组织的生成。因此,它能够催生医学研究的新工具。这些工具包括表型筛选分析、组织工程应用以及生物医学知识的全面进步。我们在此的目的是特别参照基于斑马鱼发育生物学的工具来探讨这一新兴领域。我们描述了在我们自己以及其他实验室正在开发的表型筛选分析。我们的分析包括:(i)在体内对斑马鱼全身或局部施用测试化合物或药物;(ii)随后检测或“读出”特定的表型变化。阳性读出结果可能源于测试化合物与发育途径中涉及的分子靶点结合。我们展示了针对调节骨骼模式、骨转换、免疫反应、炎症和早期生活应激的化合物分析的初步数据。这些分析使用活的斑马鱼胚胎和幼体以及正在进行尾鳍再生的成年鱼。我们描述了关于使用微载体将化合物局部靶向到再生芽基的概念验证研究。斑马鱼的饲养成本比啮齿动物低,能产出大量透明的卵,并且一些斑马鱼分析可以扩大规模用于中高通量筛选。然而,还需要在自动化和成像方面取得进展。在药物研发流程中,斑马鱼无法取代哺乳动物模型。尽管如此,它们可以在基于细胞的分析和哺乳动物全生物体模型之间提供一个具有成本效益的桥梁。

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