Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, USA.
Adv Exp Med Biol. 2020;1236:225-244. doi: 10.1007/978-981-15-2389-2_9.
Genetic model systems allow researchers to probe and decipher aspects of human disease, and animal models of disease are frequently specifically engineered and have been identified serendipitously as well. Animal models are useful for probing the etiology and pathophysiology of disease and are critical for effective discovery and development of novel therapeutics for rare diseases. Here we review the impact of animal model organism research in three examples of congenital metabolic disorders to highlight distinct advantages of model system research. First, we discuss phenylketonuria research where a wide variety of research fields and models came together to make impressive progress and where a nearly ideal mouse model has been central to therapeutic advancements. Second, we review advancements in Lesch-Nyhan syndrome research to illustrate the role of models that do not perfectly recapitulate human disease as well as the need for multiple models of the same disease to fully investigate human disease aspects. Finally, we highlight research on the GM2 gangliosidoses Tay-Sachs and Sandhoff disease to illustrate the important role of both engineered traditional laboratory animal models and serendipitously identified atypical models in congenital metabolic disorder research. We close with perspectives for the future for animal model research in congenital metabolic disorders.
遗传模型系统使研究人员能够探究和解析人类疾病的各个方面,疾病的动物模型经常被专门设计,也有偶然发现的。动物模型可用于探究疾病的病因和病理生理学,对于发现和开发罕见疾病的新型疗法至关重要。在这里,我们以三种先天性代谢紊乱的动物模型为例,回顾动物模型生物研究的影响,突出模型系统研究的独特优势。首先,我们讨论苯丙酮尿症研究,其中各种研究领域和模型汇聚在一起取得了令人瞩目的进展,而一个近乎理想的小鼠模型一直是治疗进展的核心。其次,我们回顾 Lesch-Nyhan 综合征研究的进展,说明不完全模拟人类疾病的模型的作用以及研究人类疾病各个方面需要多种相同疾病的模型。最后,我们强调 GM2 神经节苷脂贮积症 Tay-Sachs 和 Sandhoff 疾病的研究,说明传统实验室动物模型和偶然发现的非典型模型在先天性代谢紊乱研究中的重要作用。最后,我们展望先天性代谢紊乱的动物模型研究的未来前景。