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

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.

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Publication Details

Journal
Advanced NanoBiomed Research
Published
2026-07-16
DOI
https://doi.org/10.1002/anbr.202500254
Primary Topic
Urinary Bladder and Prostate Research
Type
article
Field-Weighted Citation Impact
0.00

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article

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

Nazila V. Jafari, Jennifer Rohn
Advanced NanoBiomed Research
Urinary Bladder and Prostate Research
article

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

Nazila V. Jafari, Jennifer Rohn
article en

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.

Advanced NanoBiomed Research
University College London (GB)
ConvaTec
Good health and well-being
Openalex Percentile: Top 7%
Urinary Bladder and Prostate Research
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