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Preclinical models of Wilson’s disease why dogs are catchy alternatives

机译:威尔逊氏病的临床前模型为什么狗是吸引人的替代品

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摘要

Copper toxicosis is frequently encountered in various dog breeds. A number of differences and similarities occur between Wilson disease and copper toxicosis in Bedlington terriers, caused by a mutation in the COMMD1 gene, and copper toxicosis in Labrador retrievers, caused by mutations in both ATP7A and ATP7B gene. First the specific population structure of dog breeds is explained with reference to its applicability for genetic investigations. The relatively large body size (variable from less than 1 kg to over 50 kg) and life-span (over 10 years) of dogs facilitates preclinical studies on safety on long-term effects of novel procedures. Then copper toxicosis in the two dog breeds is described in detail with an emphasis on the functions of the causative proteins. Some of the advantages of this species for preclinical studies are described with an example of liver stem cell transplantations in COMMD1 deficient dogs. Since the genetic background of copper toxicosis in other dogs’ breeds has not yet been elucidated, it is conceivable that novel copper-related gene products or modifier genes will be discovered. About a century after the Novel prize was awarded to the research on dogs (Pavlov), dogs are in spotlight again as important preclinical model animals.
机译:铜中毒在各种犬种中经常遇到。由COMMD1基因的突变引起的Wilson病和Bedlington梗犬的铜中毒和由ATP7A和ATP7B基因的突变引起的拉布拉多犬的铜中毒之间存在许多差异和相似之处。首先,参照犬种在基因研究中的适用性来解释其具体的种群结构。狗的相对较大的体型(从不到1公斤到超过50公斤不等)和寿命(超过10年)有助于进行临床研究,以研究新方法对长期安全性的安全性。然后详细描述了这两种狗的铜中毒,并着重于致病蛋白的功能。以COMMD1缺陷犬肝干细胞移植为例,描述了该物种在临床前研究中的一些优势。由于尚未阐明其他犬种中铜中毒的遗传背景,因此可以想象会发现新的铜相关基因产物或修饰基因。在将诺贝尔奖授予对狗的研究(巴甫洛夫)后大约一个世纪,狗再次成为重要的临床前模型动物而备受关注。

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