Breyer Matthew D, Böttinger Erwin, Brosius Frank C, Coffman Thomas M, Harris Raymond C, Heilig Charles W, Sharma Kumar
Division of Nephrology and Department of Medicine, Vanderbilt University Medical School, S3223 MCN, Nashville, TN 37232, USA.
J Am Soc Nephrol. 2005 Jan;16(1):27-45. doi: 10.1681/ASN.2004080648. Epub 2004 Nov 24.
Mice provide an experimental model of unparalleled flexibility for studying mammalian diseases. Inbred strains of mice exhibit substantial differences in their susceptibility to the renal complications of diabetes. Much remains to be established regarding the course of diabetic nephropathy (DN) in mice as well as defining those strains and/or mutants that are most susceptible to renal injury from diabetes. Through the use of the unique genetic reagents available in mice (including knockouts and transgenics), the validation of a mouse model reproducing human DN should significantly facilitate the understanding of the underlying genetic mechanisms that contribute to the development of DN. Establishment of an authentic mouse model of DN will undoubtedly facilitate testing of translational diagnostic and therapeutic interventions in mice before testing in humans.
小鼠为研究哺乳动物疾病提供了一个灵活性无与伦比的实验模型。近交系小鼠在对糖尿病肾脏并发症的易感性方面表现出显著差异。关于小鼠糖尿病肾病(DN)的病程以及确定那些对糖尿病肾损伤最易感的品系和/或突变体,仍有许多有待确定。通过使用小鼠中可用的独特遗传试剂(包括基因敲除和转基因小鼠),验证一个重现人类DN的小鼠模型应能显著促进对导致DN发生的潜在遗传机制的理解。建立一个真实的DN小鼠模型无疑将有助于在人体试验之前在小鼠中测试转化性诊断和治疗干预措施。