Marmorstein Alan D, Marmorstein Lihua Y
Department of Ophthalmology and Vision Science, University of Arizona, 655 North Alvernon Way, Suite 108, Tucson, AZ 85711, USA.
Trends Genet. 2007 May;23(5):225-31. doi: 10.1016/j.tig.2007.03.001. Epub 2007 Mar 26.
Macular degenerations (MD), age-related or inherited, interfere with the ability to read, drive and recognize faces. Understanding this class of diseases has been challenging because the mouse, the mammal most amenable to genetic manipulation, lacks a macula. Here we discuss whether we can model MD in the mouse, present criteria for an 'ideal' mouse model of MD and discuss how mouse models have contributed to our knowledge of MD by contrasting how well they meet the 'ideal' criteria with how informative they have actually been. By modeling MD in mice, we can learn about aspects of MD that an animal with a macula would be unable to teach us.
黄斑变性(MD),无论是年龄相关性还是遗传性的,都会影响阅读、驾驶和面部识别能力。由于最适合进行基因操作的哺乳动物小鼠没有黄斑,了解这类疾病一直具有挑战性。在这里,我们讨论是否可以在小鼠中建立MD模型,提出“理想”的MD小鼠模型标准,并通过对比小鼠模型满足“理想”标准的程度与它们实际提供的信息量,来探讨小鼠模型如何增进了我们对MD的认识。通过在小鼠中建立MD模型,我们可以了解到有黄斑的动物无法教会我们的MD相关方面的知识。