Use of laser microdissection in the analysis of renal-infiltrating T cells in MRL/lpr mice

• Published in: Modern rheumatology 2008-08, Vol.18 (4), p.385-393
• Main Authors: Wang, Yingge, Ito, Satoshi, Chino, Yusuke, Iwanami, Keiichi, Yasukochi, Takanori, Goto, Daisuke, Matsumoto, Isao, Hayashi, Taichi, Uchida, Kazuhiko, Sumida, Takayuki
• Format: Article
• Language: English
• Subjects: Histology; Kidney diseases; Lasers; Lymphocytes; Medicine; Medicine & Public Health; Original Article; Orthopedics; Rheumatology; Rodents
• ISSN: 1439-7595; 1439-7609
• DOI: 10.1007/s10165-008-0074-8

To clarify the role of T cells in the kidneys of MRL/MpJ- lpr (MRL/ lpr ) mice, cytokine mRNA expression was analyzed, and tissue localization of T cells was examined by immunohistochemistry. Cells infiltrating the glomeruli, glomerular circumference, and perivascular areas in ten female MRL/ lpr mice were captured by laser microdissection (LMD). Nested reverse transcription polymerase chain reaction (RT-PCR) of samples was performed with primers specific for β-actin, T-cell receptor β chain (TCR-Cβ), Thy-1, B220, CD4, CD8, interleukin (IL)-2, IL-4, IL-10, IL-13, IL-17, and interferon (IFN)-γ. Frozen sections of lesions were also stained immunohistochemically. B220, MAC-1, Thy-1, CD4, and CD8 staining was observed in glomeruli and perivascular areas, especially in glomerular circumference areas. T cells infiltrating the glomeruli, glomerular circumference areas, and perivascular areas produce INF-γ, IL-13, and IL-17 predominately. IL-10 positivity was identified in 60% of perivascular T cells but not in a substantial number of glomerular or periglomerular T cells. The results of our study suggest that the pathogenesis of renal lesions in MRL /lpr mice is complex and not due simply to the Th1 and Th2 balance. These findings also support the concept of different molecular mechanisms for glomerulonephritis and vasculitis in these mice.