Ganeshan Radhika, Chen Jiangli, Koch Peter J
Department of Dermatology, University of Colorado Medical School, 12800 East 19th Avenue, Aurora, CO 80045, USA.
Dermatol Res Pract. 2010;2010:584353. doi: 10.1155/2010/584353. Epub 2010 May 10.
Genetically engineered mice have been essential tools for elucidating the pathological mechanisms underlying human diseases. In the case of diseases caused by impaired desmosome function, mouse models have helped to establish causal links between mutations and disease phenotypes. This review focuses on mice that lack the desmosomal cadherins desmoglein 3 or desmocollin 3 in stratified epithelia. A comparison of the phenotypes observed in these mouse lines is provided and the relationship between the mutant mouse phenotypes and human diseases, in particular pemphigus vulgaris, is discussed. Furthermore, we will discuss the advantages and potential limitations of genetically engineered mouse lines in our ongoing quest to understand blistering skin diseases.
基因工程小鼠一直是阐明人类疾病病理机制的重要工具。对于由桥粒功能受损引起的疾病,小鼠模型有助于建立突变与疾病表型之间的因果联系。本综述聚焦于分层上皮中缺乏桥粒钙黏蛋白桥粒芯糖蛋白3或桥粒胶蛋白3的小鼠。本文对这些小鼠品系中观察到的表型进行了比较,并讨论了突变小鼠表型与人类疾病,特别是寻常型天疱疮之间的关系。此外,在我们不断探索理解水疱性皮肤病的过程中,我们将讨论基因工程小鼠品系的优势和潜在局限性。