Barnouin Karin, Tonoli Elisa, Coveney Clare, Atkinson John, Sancho Margarida, Skelton Andrew, Boocock David J, Huang Linghong, Shephard Joseph, Johnson Timothy S, Verderio Elisabetta A M, Twomey Breda
UCB Pharma, Slough, SL1 3WE, UK.
MSD, London, EC2M 6UR, UK.
Sci Rep. 2025 Apr 2;15(1):11200. doi: 10.1038/s41598-025-93894-6.
The rat sub-total nephrectomy (SNx) is a functional model of general chronic kidney disease (CKD) where the main pathological driver is glomerular hypertension representative of several subtypes of CKD. Comprehensive transcriptomics and proteomics analyses on the SNx rats were performed to identify biomarkers in plasma or urine that correlate with kidney disease and functional kidney loss. Kidneys were subjected to collagen I and III staining for fibrosis scoring, SWATH-MS proteomics and bulk RNA-sequencing transcriptomics, with SWATH-MS also performed on plasma and urine. Differential expression analysis demonstrated significant dysregulation of genes and proteins involved in fibrosis, metabolism, and immune response in the SNx rats compared to controls. Gene ontology analysis of the intersecting genes and proteins from both studies demonstrated common biology between animal cohorts that reached the predefined kidney disease thresholds (serum creatinine > two-fold or proteinuria > three-fold increase over sham-operated). Thirteen significantly differential molecules were detected with consistent directional changes in both omics datasets. These molecules were detected independently in kidney (both RNA and protein) and urine (protein only), but not in plasma. Bioinformatics analysis enabled the identification of mechanistic CKD biomarkers including lumican and collagen alpha-1(III) chain, whose co-expression has previously been both implicated in fibrosis and detected in urine in CKD patients.
大鼠次全肾切除术(SNx)是一种常见慢性肾脏病(CKD)的功能模型,其中主要的病理驱动因素是肾小球高血压,它代表了几种CKD亚型。对SNx大鼠进行了全面的转录组学和蛋白质组学分析,以确定血浆或尿液中与肾脏疾病和功能性肾损伤相关的生物标志物。对肾脏进行I型和III型胶原蛋白染色以进行纤维化评分,采用SWATH-MS蛋白质组学和批量RNA测序转录组学方法,同时也对血浆和尿液进行SWATH-MS分析。差异表达分析表明,与对照组相比,SNx大鼠中参与纤维化、代谢和免疫反应的基因和蛋白质存在显著失调。对两项研究中相交的基因和蛋白质进行基因本体分析,结果显示达到预定义肾脏疾病阈值(血清肌酐>假手术组的两倍或蛋白尿>假手术组的三倍)的动物队列之间存在共同的生物学特征。在两个组学数据集中检测到13个具有一致方向变化的显著差异分子。这些分子在肾脏(RNA和蛋白质)和尿液(仅蛋白质)中独立检测到,但在血浆中未检测到。生物信息学分析能够识别包括核心蛋白聚糖和胶原蛋白α-1(III)链在内的CKD机制生物标志物,它们的共表达先前已被认为与纤维化有关,并且在CKD患者的尿液中也被检测到。