Verstege Marleen I, ten Kate Fiebo J W, Reinartz Susanne M, van Drunen Cornelis M, Slors Frederik J M, Bemelman Willem A, Vyth-Dreese Florry A, te Velde Anje A
Centre for Experimental and Molecular Medicine, Academic Medical Centre, Amsterdam, The Netherlands.
J Histochem Cytochem. 2008 Mar;56(3):233-41. doi: 10.1369/jhc.7A7308.2007. Epub 2007 Nov 26.
Dendritic cells (DCs) are key cells in innate and adaptive immune responses that determine the pathophysiology of Crohn's disease. Intestinal DCs migrate from the mucosa into mesenteric lymph nodes (MLNs). A number of different markers are described to define the DC populations. In this study we have identified the phenotype and localization of intestinal and MLN DCs in patients with Crohn's disease and non-IBD patients based on these markers. We used immunohistochemistry to demonstrate that all markers (S-100, CD83, DC-SIGN, BDCA1-4, and CD1a) showed a different staining pattern varying from localization in T-cell areas of lymph follicles around blood vessels or single cells in the lamina propria and in the MLN in the medullary cords and in the subcapsular sinuses around blood vessels and in the T-cell areas. In conclusion, all different DC markers give variable staining patterns so there is no marker for the DC.
树突状细胞(DCs)是先天性和适应性免疫反应中的关键细胞,决定了克罗恩病的病理生理学。肠道DCs从黏膜迁移至肠系膜淋巴结(MLNs)。已有多种不同标志物用于定义DC群体。在本研究中,我们基于这些标志物确定了克罗恩病患者及非炎症性肠病(IBD)患者肠道和MLN中DCs的表型及定位。我们采用免疫组化法证明,所有标志物(S-100、CD83、DC-SIGN、BDCA1-4和CD1a)均呈现出不同的染色模式,从血管周围淋巴滤泡的T细胞区域定位到固有层中的单个细胞,以及MLN的髓索、血管周围的被膜下窦和T细胞区域。总之,所有不同的DC标志物均呈现出可变的染色模式,因此不存在DC的特异性标志物。