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May 3, 20260 citations

Role of Bruton's Tyrosine Kinase in mast cell driven urothelial barrier injury in an LL-37 induced model of interstitial cystitis.

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GWGuang WangBLBin-Sen LiJCJin-Yi Chu

Key Points

  • This research aims to explore the role of Bruton's tyrosine kinase (BTK) in mast cell activation and bladder inflammation related to interstitial cystitis/bladder pain syndrome (IC/BPS).
  • Established an LL-37-induced IC/BPS rat model and in vitro mast cell co-culture system.
  • Modulated BTK expression using adenoviral vectors and cell transfection techniques.
  • Assessed bladder inflammation, mast cell degranulation, and urothelial barrier function through histology, ELISA, RT-qPCR, and other biochemical assays.
  • LL-37 increased BTK expression in IC/BPS rats, promoting inflammation and urothelial damage.
  • BTK overexpression worsened the inflammatory response and urothelial barrier disruption; knockdown improved these outcomes.
  • In vitro experiments showed that LL-37 enhanced mast cell proliferation and degranulation, decreasing tight junction proteins in SV-HUC-1 cells.

Abstract

Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic urinary disorder with unclear pathogenesis. Previous studies identified BTK as a hub gene potentially involved in IC/BPS. This study investigates BTK's role in mast cell (MC) activation and bladder inflammation. An LL-37-induced IC/BPS rat model and an in vitro MCs Co-culture system were established. BTK expression was modulated via adenoviral vectors and cell transfection. Bladder inflammation, MC degranulation, and urothelial barrier function were assessed using histology, ELISA, RT-qPCR, Western blot, IHC, TEM, and IF. MC function was evaluated via CCK-8, flow cytometry, Transwell, and TEM. LL-37 upregulated BTK in IC/BPS rats, promoting inflammation, cytokine release, collagen deposition, MC degranulation, and urothelial damage. BTK overexpression exacerbated, while knockdown alleviated these effects. In vitro, LL-37 stimulated MC proliferation, invasion, and degranulation, and reduced apoptosis. Co-culture with activated MCs decreased glycosaminoglycan (GAG) and tight junction (TJ) proteins in SV-HUC-1 cells, enhanced by BTK overexpression and reversed by knockdown. BTK promotes LL-37-induced MC activation and urothelial barrier disruption by suppressing GAGs and TJ proteins, contributing to IC/BPS pathophysiology.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/69f6e60f8071d4f1bdfc6ad6https://doi.org/10.1038/s41598-026-50443-z
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