Department of Medicine B, University of Münster, Münster, Germany.
Clin Exp Immunol. 2010 Jun;160(3):440-9. doi: 10.1111/j.1365-2249.2010.04103.x. Epub 2010 Feb 10.
The chemokine receptor CCR6 is expressed by dendritic cells, B and T cells predominantly within the organized structures of the gut-associated lymphatic tissue. Its ligand CCL20 is synthesized by the follicle-associated epithelium and is crucial for the development of M cells within Peyer's patches. In addition, lineage-negative c-kit positive lymphocytes within cryptopatches (CP) express CCR6. CCR6-deficient mice exhibit an altered intestinal immune system containing increased amounts of intraepithelial lymphocytes and show smaller Peyer's patches, while progression of cryptopatches to mature isolated lymphoid follicles (ILF) is inhibited. In this report, we show that lin(-) c-kit(+) lymphocytes express a variety of different chemokine receptors and that CCR6 identifies those cells located within CP. In contrast, cells found outside CP are positive for CXCR3 and exhibit a different surface marker profile, suggesting that at least two different populations of lin(-) c-kit(+) cells are present. The presence of CCR6 does not influence the expression of Notch molecules on lin(-) c-kit(+) cells, nor does it influence Notch ligand expression on bone marrow-derived dendritic cells. In the human gut, CCR6 identifies clusters of lymphocytes resembling murine CP. CCR6 seems to have an important role for lin(-) c-kit(+) cells inside CP, is expressed in a regulated manner and identifies potential human CP.
趋化因子受体 CCR6 主要由肠道相关淋巴组织的树突状细胞、B 细胞和 T 细胞表达。其配体 CCL20 由滤泡相关上皮细胞合成,对派尔集合淋巴结中 M 细胞的发育至关重要。此外,隐窝内的谱系阴性 c-kit 阳性淋巴细胞(CP)表达 CCR6。CCR6 缺陷小鼠表现出改变的肠道免疫系统,其中上皮内淋巴细胞数量增加,并显示出较小的派尔集合淋巴结,而隐窝向成熟的孤立淋巴滤泡(ILF)的进展受到抑制。在本报告中,我们表明 lin(-) c-kit(+) 淋巴细胞表达多种不同的趋化因子受体,并且 CCR6 可识别位于 CP 内的细胞。相比之下,位于 CP 外的细胞对 CXCR3 呈阳性反应,并表现出不同的表面标记特征,这表明至少存在两种不同的 lin(-) c-kit(+) 细胞群体。CCR6 的存在不会影响 lin(-) c-kit(+) 细胞上 Notch 分子的表达,也不会影响骨髓来源的树突状细胞上 Notch 配体的表达。在人类肠道中,CCR6 可识别类似于小鼠 CP 的淋巴细胞簇。CCR6 似乎在 CP 内的 lin(-) c-kit(+) 细胞中具有重要作用,其表达受到调节,并可识别潜在的人类 CP。