Department of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.
Am J Physiol Renal Physiol. 2010 Jun;298(6):F1484-91. doi: 10.1152/ajprenal.00002.2010. Epub 2010 Mar 10.
Chronic kidney disease is a growing medical concern, with an estimated 25.6 million people in the United States exhibiting some degree of kidney injury and/or decline in kidney function. Animal models provide great insight into the study of the genetics of complex diseases. In particular, heterogeneous stock (HS) rats represent a unique genetic resource enabling rapid fine-mapping of complex traits. However, they have not been explored as a model to study renal phenotypes. To evaluate the usefulness of HS rats in the genetics of renal traits, a time course evaluation (weeks 8-40) was performed for several renal phenotypes. As expected, a large degree of variation was seen for most renal traits. By week 24, three (of 40) rats exhibited marked proteinuria that increased gradually until week 40 and ranged from 33.7 to 80.2 mg/24 h. Detailed histological analysis confirmed renal damage in these rats. In addition, several rats consistently exhibited significant hematuria (5/41). Interestingly, these rats were not the same rats that exhibited proteinuria, indicating that susceptibility to different types of kidney injury is likely segregating within the HS population. One HS rat exhibited unilateral renal agenesis (URA), which was accompanied by a significant degree of proteinuria and glomerular and tubulointerstitial injury. The parents of this HS rat were identified and bred further. Additional offspring of this pair were observed to exhibit URA at frequency between 40% and 60%. In summary, these novel data demonstrate that HS rats exhibit variation in proteinuria and other kidney-related traits, confirming that the model harbors susceptibility alleles for kidney injury and providing the basis for further genetic studies.
慢性肾脏病是一个日益严重的医学问题,据估计,美国有 2560 万人患有不同程度的肾脏损伤和/或肾功能下降。动物模型为复杂疾病的遗传学研究提供了重要的见解。特别是,异质品系(HS)大鼠代表了一种独特的遗传资源,能够快速精细地对复杂性状进行定位。然而,它们尚未被探索作为研究肾脏表型的模型。为了评估 HS 大鼠在肾脏表型遗传学研究中的有用性,对几种肾脏表型进行了为期 8-40 周的时间进程评估。正如预期的那样,大多数肾脏表型都存在很大程度的差异。到第 24 周,有 3 只(40 只中的 3 只)大鼠出现明显的蛋白尿,逐渐增加,直到第 40 周,范围从 33.7 到 80.2mg/24h。详细的组织学分析证实了这些大鼠的肾脏损伤。此外,有几只大鼠持续出现明显的血尿(41 只中的 5 只)。有趣的是,这些大鼠不是出现蛋白尿的相同大鼠,这表明对不同类型的肾损伤的易感性可能在 HS 群体中分离。一只 HS 大鼠出现单侧肾发育不全(URA),伴有明显程度的蛋白尿和肾小球和肾小管间质损伤。这只 HS 大鼠的父母被鉴定并进一步繁殖。这对夫妇的其他后代也观察到 URA 的发生率在 40%到 60%之间。总之,这些新数据表明,HS 大鼠在蛋白尿和其他肾脏相关性状方面存在差异,证实了该模型携带有肾脏损伤的易感等位基因,并为进一步的遗传研究提供了基础。