Modeling Catheter-Associated Bladder Mucosal Adhesion and Microtrauma Using a Human Urothelial Microtissue Model

IF 4.8 Q2 ENGINEERING, BIOMEDICAL
Advanced Nanobiomed Research Pub Date : 2026-10-01 Epub Date: 2026-07-16 DOI:10.1002/anbr.202500254
Nazila V. Jafari, Jennifer L. Rohn
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引用次数: 0

Abstract

Animal models have been used to investigate urinary tract catheters, but small animals do not accurately recapitulate human bladder physiology nor support different types of catheters. Recent advances in three-dimensional models mimicking tissue microenvironments have improved our understanding of human tissue development and allowed us to model many diseases. Here, our objective was to characterise bladder urothelial mucoadhesion and microtrauma associated with intermittent catheterisation. We employed our three-dimensional Urine-tolerant Human Urothelial model (3D-UHU) to investigate two different intermittent catheter types, a polyvinylpyrrolidone (PVP)-coated catheter (PVP-CC) and a coating-free integrated amphiphilic surfactant (IAS) catheter. We showed that pressing catheters onto the models for 2 min caused compression of the 3D-UHU model in contact regions, with disruption of urothelial umbrella cells detected by immunofluorescence staining of surface markers uroplakin III, cytokeratin 20 and chondroitin sulphate, alongside occasional effacement of apical surfaces exposing intermediate layers. PVP-CC had a significantly higher number of urothelial cells adhered to its surface after catheter removal compared with IAS. Moreover, application and removal of PVP-CC caused a decrease in transepithelial electrical resistance, suggesting barrier disruption, whereas IAS did not cause a statistically different effect. However, no change in paracellular permeability rates assessed by FITC-dextran were observed in models after application of catheter pieces. Finally, compression of models induced trauma-triggered inflammatory cytokine responses. Specifically, we observed increased secretion of the pro-inflammatory cytokine IL-1β as well as the cell adhesion molecule CEACAM1 after exposure to PVP-CC compared with IAS. These data demonstrate that the 3D-UHU model holds promise as an alternative to animal models for investigating the effects of urinary catheters on the urothelium.

用人类尿路上皮显微组织模型模拟导管相关膀胱粘膜粘连和微创伤
动物模型已被用于研究尿路导尿管,但小动物不能准确地概括人类膀胱生理,也不能支持不同类型的导尿管。模拟组织微环境的三维模型的最新进展提高了我们对人体组织发育的理解,并使我们能够模拟许多疾病。在这里,我们的目的是表征膀胱尿路上皮黏附和微创伤与间歇性导尿。我们采用三维尿耐受性人尿路上皮模型(3D-UHU)来研究两种不同类型的间歇导管,一种是聚乙烯吡咯烷酮(PVP)涂层导管(PVP- cc),另一种是无涂层集成两亲性表面活性剂(IAS)导管。我们发现,将导管压在模型上2分钟会导致3D-UHU模型在接触区域受到压迫,通过表面标记物uroplakin III、细胞角蛋白20和硫酸软骨素的免疫荧光染色检测到尿路上皮保护伞细胞的破坏,同时偶尔出现根尖表面的消失,露出中间层。PVP-CC与IAS相比,拔管后其表面粘附的尿路上皮细胞数量明显增加。此外,PVP-CC的应用和去除引起了上皮电阻的降低,表明屏障破坏,而IAS没有引起统计学上不同的效果。然而,应用导管片后,模型中未观察到fitc -葡聚糖评估的细胞旁通透率的变化。最后,压缩模型诱导创伤引发的炎症细胞因子反应。具体来说,我们观察到与IAS相比,暴露于PVP-CC后,促炎细胞因子IL-1β和细胞粘附分子CEACAM1的分泌增加。这些数据表明,3D-UHU模型有望替代动物模型,用于研究导尿管对尿路上皮的影响。
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来源期刊
Advanced Nanobiomed Research
Advanced Nanobiomed Research nanomedicine, bioengineering and biomaterials-
CiteScore
5.00
自引率
5.90%
发文量
87
审稿时长
21 weeks
期刊介绍: Advanced NanoBiomed Research will provide an Open Access home for cutting-edge nanomedicine, bioengineering and biomaterials research aimed at improving human health. The journal will capture a broad spectrum of research from increasingly multi- and interdisciplinary fields of the traditional areas of biomedicine, bioengineering and health-related materials science as well as precision and personalized medicine, drug delivery, and artificial intelligence-driven health science. The scope of Advanced NanoBiomed Research will cover the following key subject areas: ▪ Nanomedicine and nanotechnology, with applications in drug and gene delivery, diagnostics, theranostics, photothermal and photodynamic therapy and multimodal imaging. ▪ Biomaterials, including hydrogels, 2D materials, biopolymers, composites, biodegradable materials, biohybrids and biomimetics (such as artificial cells, exosomes and extracellular vesicles), as well as all organic and inorganic materials for biomedical applications. ▪ Biointerfaces, such as anti-microbial surfaces and coatings, as well as interfaces for cellular engineering, immunoengineering and 3D cell culture. ▪ Biofabrication including (bio)inks and technologies, towards generation of functional tissues and organs. ▪ Tissue engineering and regenerative medicine, including scaffolds and scaffold-free approaches, for bone, ligament, muscle, skin, neural, cardiac tissue engineering and tissue vascularization. ▪ Devices for healthcare applications, disease modelling and treatment, such as diagnostics, lab-on-a-chip, organs-on-a-chip, bioMEMS, bioelectronics, wearables, actuators, soft robotics, and intelligent drug delivery systems. with a strong focus on applications of these fields, from bench-to-bedside, for treatment of all diseases and disorders, such as infectious, autoimmune, cardiovascular and metabolic diseases, neurological disorders and cancer; including pharmacology and toxicology studies.
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