Hum Mol Genet. 2013 Oct 15;22(20):4148-63. doi: 10.1093/hmg/ddt263. Epub 2013 Jun 6.
Uromodulin-associated kidney disease (UAKD) is a dominant heritable renal disease in humans which is caused by mutations in the uromodulin (UMOD) gene and characterized by heterogeneous clinical appearance. To get insights into possible causes of this heterogeneity of UAKD, we describe the new mutant mouse line Umod(C93F), leading to disruption of a putative disulfide bond which is also absent in a known human UMOD mutation, and compare the phenotype of this new mouse line with the recently published mouse line Umod(A227T). In both mutant mouse lines, which were both bred on the C3H background, the Umod mutations cause a gain-of-toxic function due to a maturation defect of the mutant uromodulin leading to a dysfunction of thick ascending limb of Henle's loop (TALH) cells of the kidney. Umod mutant mice exhibit increased plasma urea and Cystatin levels, impaired urinary concentration ability, reduced fractional excretion of uric acid and nephropathological alterations including uromodulin retention in TALH cells, interstitial fibrosis and inflammatory cell infiltrations, tubular atrophy and occasional glomerulo- und tubulocystic changes, a phenotype highly similar to UAKD in humans. The maturation defect of mutant uromodulin leads to the accumulation of immature uromodulin in the endoplasmic reticulum (ER) and to ER hyperplasia. Further, this study was able to demonstrate for the first time in vivo that the severity of the uromodulin maturation defect as well as onset and speed of progression of renal dysfunction and morphological alterations are strongly dependent on the particular Umod mutation itself and the zygosity status.
尿调蛋白相关性肾病(UAKD)是一种人类显性遗传性肾脏疾病,由尿调蛋白(UMOD)基因突变引起,其临床表现具有异质性。为了深入了解 UAKD 异质性的可能原因,我们描述了一种新的突变小鼠品系 Umod(C93F),该突变导致一个假定的二硫键破坏,而该突变在已知的人类 UMOD 突变中也不存在,并比较了该新小鼠品系与最近发表的 Umod(A227T)小鼠品系的表型。在这两个突变小鼠品系中,突变均发生在 C3H 背景下,由于突变尿调蛋白的成熟缺陷导致其毒性功能获得,从而导致肾脏的 Henle 升支粗段(TALH)细胞功能障碍。Umod 突变小鼠表现出血浆尿素和胱抑素水平升高、尿浓缩能力受损、尿酸排泄分数降低以及肾脏病理改变,包括 TALH 细胞中尿调蛋白的蓄积、间质纤维化和炎症细胞浸润、肾小管萎缩和偶尔出现的肾小球和肾小管囊状改变,这些表型与人类 UAKD 高度相似。突变尿调蛋白的成熟缺陷导致未成熟尿调蛋白在内质网(ER)中蓄积和 ER 增生。此外,本研究首次在体内证明,尿调蛋白成熟缺陷的严重程度以及肾功能和形态改变的发病和进展速度强烈依赖于特定的 Umod 突变本身及其杂合状态。