Hosur Vishnu, Low Benjamin E, Avery Cindy, Shultz Leonard D, Wiles Michael V
The Jackson Laboratory, Bar Harbor 04609, Maine.
J Cell Biochem. 2017 Oct;118(10):3043-3048. doi: 10.1002/jcb.26002. Epub 2017 May 15.
Mice are the most commonly used model organisms to study human disease. Many genetic human diseases can be recapitulated by modifying the mouse genome allowing the testing of existing and novel therapeutics, including combinatorial therapeutics, without putting humans at risk. Specifically, the development of "humanized" mice, that is, severely immunodeficient mice engrafted with functional human hematopoietic and immune cells and tissues, has revolutionized our ability to study and model human diseases in preclinical in vivo systems. Until recently it has been challenging to develop strains of humanized mice with targeted mutations or that transgenically express human genes with site-specific mutations, and can permit optimal growth of functional human cells and tissues. However, recent advances in targeted nuclease-based genetic engineering have enabled precise modification and development of humanized mouse models at an unprecedented pace. These modifications permit optimal growth of functional human cells and tissues and can be used to replicate human genetically determined diseases. J. Cell. Biochem. 118: 3043-3048, 2017. © 2017 Wiley Periodicals, Inc.
小鼠是研究人类疾病最常用的模式生物。通过修饰小鼠基因组可以重现许多人类遗传疾病,从而能够在不危及人类的情况下测试现有的和新型的治疗方法,包括联合治疗。具体而言,“人源化”小鼠的开发,即植入功能性人类造血和免疫细胞及组织的严重免疫缺陷小鼠,彻底改变了我们在临床前体内系统中研究和模拟人类疾病的能力。直到最近,开发具有靶向突变或转基因表达具有位点特异性突变的人类基因、并能使功能性人类细胞和组织实现最佳生长的人源化小鼠品系一直具有挑战性。然而,基于靶向核酸酶的基因工程的最新进展使得以前所未有的速度精确修饰和开发人源化小鼠模型成为可能。这些修饰能使功能性人类细胞和组织实现最佳生长,并可用于复制人类基因决定的疾病。《细胞生物化学杂志》118: 3043 - 3048, 2017年。© 2017威利期刊公司。