Biochemistry Unit, Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Department of Biomolecular Medicine, Center of Medical Genetics, Ghent University-University Hospital, Ghent, Belgium.
Front Endocrinol (Lausanne). 2020 Jul 31;11:489. doi: 10.3389/fendo.2020.00489. eCollection 2020.
Animal models are essential tools for addressing fundamental scientific questions about skeletal diseases and for the development of new therapeutic approaches. Traditionally, mice have been the most common model organism in biomedical research, but their use is hampered by several limitations including complex generation, demanding investigation of early developmental stages, regulatory restrictions on breeding, and high maintenance cost. The zebrafish has been used as an efficient alternative vertebrate model for the study of human skeletal diseases, thanks to its easy genetic manipulation, high fecundity, external fertilization, transparency of rapidly developing embryos, and low maintenance cost. Furthermore, zebrafish share similar skeletal cells and ossification types with mammals. In the last decades, the use of both forward and new reverse genetics techniques has resulted in the generation of many mutant lines carrying skeletal phenotypes associated with human diseases. In addition, transgenic lines expressing fluorescent proteins under bone cell- or pathway- specific promoters enable imaging of differentiation and signaling at the cellular level. Despite the small size of the zebrafish, many traditional techniques for skeletal phenotyping, such as x-ray and microCT imaging and histological approaches, can be applied using the appropriate equipment and custom protocols. The ability of adult zebrafish to remodel skeletal tissues can be exploited as a unique tool to investigate bone formation and repair. Finally, the permeability of embryos to chemicals dissolved in water, together with the availability of large numbers of small-sized animals makes zebrafish a perfect model for high-throughput bone anabolic drug screening. This review aims to discuss the techniques that make zebrafish a powerful model to investigate the molecular and physiological basis of skeletal disorders.
动物模型是解决骨骼疾病基础科学问题和开发新治疗方法的重要工具。传统上,小鼠一直是生物医学研究中最常见的模式生物,但由于其存在复杂的生成过程、早期发育阶段的研究要求高、繁殖受到监管限制以及高维护成本等限制,其应用受到了阻碍。斑马鱼作为一种有效的替代脊椎动物模型,已被用于研究人类骨骼疾病,这要归功于其易于遗传操作、高繁殖力、体外受精、快速发育胚胎的透明性以及低维护成本。此外,斑马鱼与哺乳动物具有相似的骨骼细胞和骨化类型。在过去的几十年中,使用正向和新的反向遗传学技术已经产生了许多携带与人类疾病相关的骨骼表型的突变系。此外,表达在骨细胞或途径特异性启动子下的荧光蛋白的转基因系能够在细胞水平上对分化和信号进行成像。尽管斑马鱼体型较小,但许多传统的骨骼表型技术,如 X 射线和微 CT 成像以及组织学方法,都可以使用适当的设备和定制的方案进行应用。成年斑马鱼重塑骨骼组织的能力可以被用作研究骨形成和修复的独特工具。最后,胚胎对溶解在水中的化学物质的通透性,以及大量小型动物的存在,使得斑马鱼成为高通量骨合成药物筛选的理想模型。本文旨在讨论使斑马鱼成为研究骨骼疾病分子和生理基础的强大模型的技术。