Uroepithelial cells can directly respond to Mycobacterium bovis bacillus Calmette-Guérin through Toll-like receptor signalling
Article first published online: 9 MAR 2006
Volume 97, Issue 4, pages 860–864, April 2006
How to Cite
MIYAZAKI, J., KAWAI, K., OIKAWA, T., JOHRAKU, A., HATTORI, K., SHIMAZUI, T. and AKAZA, H. (2006), Uroepithelial cells can directly respond to Mycobacterium bovis bacillus Calmette-Guérin through Toll-like receptor signalling. BJU International, 97: 860–864. doi: 10.1111/j.1464-410X.2006.06026.x
- Issue published online: 9 MAR 2006
- Article first published online: 9 MAR 2006
- Accepted for publication 12 October 2005
- Toll-like receptor;
- uroepithelial cells;
- Mycobacterium bovis;
- urinary cytokine
To investigate, in a human urinary tract cell line, the interaction of Toll-like receptor (TLR) signals with cytoplasmic adapter proteins MyD88 and bacillus Calmette-Guérin (BCG), and evaluate the epithelial cytokine response to BCG infection. Intravesical BCG therapy is effective against carcinoma in situ and as prophylaxis for recurrence, but although immunological mechanisms have been assumed, the mechanisms of the antitumour effects of BCG have not been completely elucidated.
MATERIALS AND METHODS
The cell line was first screened for TLR expression by reverse transcription-polymerase chain reaction (RT-PCR). Total RNA was isolated from a human urinary cell line, Hu35E6E7, and cDNA synthesised. PCR was used to measure the gene expression of TLR-2, -3, -4, -5, -9, MyD88, MD-2, CD14 and interleukin-8 and -6. The Hu35E6E7 cell line was cultured in keratinocyte serum-free medium, and BCG was added to the cell culture. After Hu35E6E7 cells were stimulated by BCG for various periods, the total RNA of the cells was extracted. Quantitative real-time PCR was conducted for MyD88 using appropriate probes, and the expression of MyD88 analysed. The cell supernatant was collected, and the levels of interferon-γ, tumour necrosis factor-α, interleukin-2, -12, -4, -6, -10, -8 and -1β were assayed using an enzyme-linked immunosorbent assay.
Uroepithelial cells expressed TLR-2, -3, -4 and -9, and MyD88, MD2, CD14, interleukin-6 and -8 were also detected. At 3, 6, 9 and 12 h after adding BCG, quantitative PCR assay showed that the expression of MyD88 was maximal at 6 h. The presence of BCG stimulated the release only of interleukin-6 and -8 from Hu35E6E7 cells after 6 h. By contrast, interferon-γ, tumour necrosis factor-α, interleukin-2, -12, -4, -10 and -1β were not detected in the culture supernatant.
These results show that uroepithelial cells, but not immune cells, responded directly to BCG through TLR signalling. Further investigation is needed to determine the role of cytokines released from uroepithelial cells after BCG infection.