Quantitative Proteome of Infant Stenotic Ureters Reveals Extracellular Matrix Organization and Oxidative Stress Dysregulation Underlying Ureteropelvic Junction Obstruction. Issue 6 (19th October 2020)

• Record Type: Journal Article
• Authors: Li, Yueyan; Chen, Zhoutong; Zhang, Junqi; Zhang, Qimin; He, Lei; Xu, Maosheng; Xu, Guofeng; Geng, Hongquan; Fang, Xiaoliang
• Is Part Of: Proteomics. Volume 14:Issue 6(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-10-19
• Subjects: congenital hydronephrosis -- extracellular matrix -- oxidative stress -- proteomics -- ureteropelvic junction obstruction; Proteomics -- Periodicals; 572.605
• DOI: 10.1002/prca.202000030
• Languages: English
• ISSNs: 1862-8346

Abstract

Abstract : Purpose: Ureteropelvic junction obstruction (UPJO) is the most frequent cause of congenital hydronephrosis in child. To better investigate the molecular mechanisms of this pathological process, the stenotic ureter proteome of UPJO in infants is compared with their own normal pre‐stenotic segments. Experimental Design: Data independent acquisition‐based proteomics are performed to compare proteome between pre‐stenotic and stenotic ureter from nine UPJO infants. Gene ontology analysis, hierarchical cluster analysis, and network interaction are performed to characterize biological functions of significantly altered proteins. Selected significantly altered proteins are validated by western blot on another three UPJO infants. Results: 15 proteins are up‐regulated and 33 proteins are down‐regulated during stenotic pathology. Significantly altered proteins are involved in decreased extracellular matrix and cytoskeleton organization, increased regulation of oxidative activity, and altered inflammatory associated exocytosis. Significant expression of biglycan, fibulin‐1, myosin‐10, cytochrome b5 are validated providing possible mechanism in UPJO which could be associated impaired smooth muscle cell, epithelial integrity, and increased oxidative stress. Conclusions and Clinical Relevance: This study provides molecular evidence of dysregulated extracellular matrix organization, impaired smooth muscle cell, and oxidative stress during UPJO pathology, indicating that biglycan, fibulin‐1, myosin‐10, cytochrome b5 might reflect the pathology of UPJO.