Abstract
PURPOSE: The aim of this study was to investigate whether pathologic changes in zonula occludens-1 (ZO-1) are induced by interleukin-13 (IL-13) in the experimental minimal-change nephrotic syndrome (MCNS) model and to determine whether montelukast, a leukotriene receptor antagonist, has an effect on ZO-1 restoration in cultured human podocytes.
MATERIALS AND METHODS: Human podocytes cultured on bovine serum albumin-coated plates were treated with different doses of IL-13 and montelukast and then examined for distribution using confocal microscopy and for ZO-1 protein levels using Western blotting.
RESULTS: ZO-1 was internalized and shown to accumulate in the cytoplasm of human podocytes in an IL-13 dose-dependent manner. High doses (50 and 100 ng/mL) of IL-13 decreased the levels of ZO-1 protein at 12 and 24 h (both p<0.01; n=3), which were significantly reversed by a high dose (0.5 μM) montelukast treatment (p<0.01; n=3).
CONCLUSION: Our results suggest that IL-13 alters the expression of ZO-1, and such alterations in the content and distribution of ZO-1 may be relevant in the pathogenesis of proteinuria in the MCNS model.
Original language | English |
---|---|
Pages (from-to) | 426-32 |
Number of pages | 7 |
Journal | Yonsei Medical Journal |
Volume | 56 |
Issue number | 2 |
DOIs | |
Publication status | Published - Mar 2015 |
Keywords
- Acetates
- Blotting, Western
- Dose-Response Relationship, Drug
- Humans
- Interleukin-13
- Leukotriene Antagonists
- Microscopy, Confocal
- Podocytes
- Proteinuria
- Quinolines
- Tight Junctions
- Zonula Occludens-1 Protein