Division of Pediatric Urology, University Medical Center Regensburg, Klinik St. Hedwig, Steinmetzstraße 1-3, Regensburg, 93049, Germany; Department of Urology, University Medical Center Frankfurt, Theodor-Stern-Kai 7, Frankfurt, 60590, Germany.
Institute for Pathology, Dechbettener Strasse 5, Regensburg, 93049, Germany.
J Pediatr Urol. 2021 Oct;17(5):632.e1-632.e7. doi: 10.1016/j.jpurol.2021.07.016. Epub 2021 Jul 24.
We have previously characterised the urothelium from infants with classic bladder exstrophy (CBE) for the expression of urothelial differentiation-associated markers. We found abnormal expression patterns of uroplakin 3a, cytokeratin 13, cytokeratin 20 and claudin 4 in the majority of bladder biopsies taken at the time of primary bladder closure. Abnormal urothelial differentiation results in a compromised urothelial barrier with potential implications on bladder development and the success of reconstructive surgery.
To investigate whether the urothelial differentiation changes observed in the unclosed exstrophic bladder persist after successful primary exstrophy repair.
DESIGN, SETTING AND PARTICIPANTS: From 2005 to 2018 bladder biopsies from 115 children with CBE obtained at the time of primary bladder closure (n = 67, median age: 8.1 weeks) and during secondary procedures aimed at achieving continence (n = 48, median age: 6.8 years) were prospectively collected. Following histological assessment immunohistochemistry was used to investigate the expression of uroplakin 3a, cytokeratin 13 and 20 and claudin 4, well-characterized markers associated with the terminally-differentiated, fully functional urothelial phenotype. The urothelium from 16 children with VUR and with non-refluxing disorders of the urinary tract served as controls.
Tissue specimen from 100 children were included in the analysis. Only 32% of bladder specimens from children having undergone successful primary bladder closure in early infancy displayed a fully differentiated urothelial phenotype with regular expression of all 4 markers. The remaining bladders revealed irregular or absent marker expression suggesting abnormal urothelial differentiation. 86% of the samples had inflammatory, proliferative or metaplastic histological changes.
Our results suggest persisting urothelial differentiation changes in two-thirds of exstrophic bladders following successful bladder closure in early infancy. Despite some limitations, the findings provide a platform for translational studies into the role of the urothelium for the developmental potential of the exstrophic bladder and the success of reconstructive surgery.
我们之前已经研究了经典膀胱外翻(CBE)患儿的尿路上皮,以确定其尿路上皮分化相关标志物的表达情况。我们发现,在初次膀胱关闭时采集的大多数膀胱活检中,桥粒蛋白 3a、细胞角蛋白 13、细胞角蛋白 20 和紧密连接蛋白 4 的表达模式异常。尿路上皮分化异常会导致尿路上皮屏障受损,这可能会对膀胱发育和重建手术的成功产生影响。
研究在初次膀胱外翻修复成功后,未闭合的外翻膀胱中观察到的尿路上皮分化变化是否持续存在。
设计、设置和参与者:从 2005 年到 2018 年,前瞻性收集了 115 例 CBE 患儿初次膀胱关闭时(n=67,中位年龄:8.1 周)和为实现控尿而进行的二次手术时(n=48,中位年龄:6.8 岁)的膀胱活检。经过组织学评估,使用免疫组织化学方法检测桥粒蛋白 3a、细胞角蛋白 13 和 20 以及紧密连接蛋白 4 的表达情况,这些标志物是与终末分化、完全功能的尿路上皮表型相关的特征性标志物。16 例伴有 VUR 和非反流性尿路疾病的儿童的尿路上皮作为对照组。
100 例患儿中有 100 例组织标本纳入分析。只有 32%的在婴儿早期成功进行初次膀胱关闭的患儿的膀胱标本表现出完全分化的尿路上皮表型,所有 4 种标志物的表达均正常。其余的膀胱显示出异常或缺失标志物表达,提示尿路上皮分化异常。86%的样本存在炎症、增殖或化生的组织学改变。
我们的研究结果表明,在婴儿早期成功进行初次膀胱关闭后,2/3的外翻膀胱仍存在尿路上皮分化变化。尽管存在一些局限性,这些发现为研究尿路上皮在膀胱外翻的发育潜力和重建手术成功中的作用提供了一个转化研究的平台。