Department of Experimental Immunology, Medical University of Łódź, Pomorska 251, 92-213 Łódź, Poland.
Mediators Inflamm. 2011;2011:427473. doi: 10.1155/2011/427473. Epub 2011 May 2.
The aim of our study was to determine whether some bacterial components as well as some proinflammatory cytokines can affect surface mast cell levels. By the use of flow cytometry technique, we documented that freshly isolated mature rat peritoneal mast cells do express surface TLR2 and TLR4 protein, but not CD14 molecules, and respond to stimulation with TLR2 and TLR4 ligands by cysteinyl leukotriene generation. The level of TLR2 protein is modulated by PGN and CCL5 treatment, but not by LPS, LAM, TNF, or IL-6. Surface mast cell TLR4 expression is affected by LPS, LAM, IL-6, and CCL5. Considering that TLR-mediated activation conditions not only engaged these cells in antibacterial defense and development of inflammation but also might influence allergic processes, our observations that surface TLR2 and TLR4 expression can be regulated both bacterial components and proinflammatory cytokines seem to be very intriguing and importance.
我们研究的目的是确定某些细菌成分和某些促炎细胞因子是否会影响表面肥大细胞水平。通过使用流式细胞术技术,我们记录到新鲜分离的成熟大鼠腹腔肥大细胞确实表达表面 TLR2 和 TLR4 蛋白,但不表达 CD14 分子,并且对 TLR2 和 TLR4 配体的刺激通过半胱氨酸白三烯的产生作出反应。TLR2 蛋白的水平可通过 PGN 和 CCL5 处理进行调节,但不受 LPS、LAM、TNF 或 IL-6 的影响。表面肥大细胞 TLR4 表达受 LPS、LAM、IL-6 和 CCL5 的影响。鉴于 TLR 介导的激活条件不仅使这些细胞参与抗菌防御和炎症发展,而且可能影响过敏过程,我们观察到表面 TLR2 和 TLR4 的表达可以受到细菌成分和促炎细胞因子的调节,这似乎非常有趣和重要。