Ogata T, Yamakawa M, Imai Y, Takahashi T
Second Department of Pathology, Yamagata University School of Medicine, Japan.
Blood. 1996 Oct 15;88(8):2995-3003.
The expression of adhesion molecules on human tonsillar follicular dendritic cells (FDCs) in the secondary lymphoid follicle (LF) in vivo and in vitro was investigated using cryostat sections and cytospin preparations of FDCs isolated with a magnetic cell sorter, respectively. FDCs were immunochemically positive for Mac-1 (CD11b), sialyl-Lex (CD15s), CD22, integrin beta 1 (CD29), CD40, very late activation antigen (VLA)-alpha 3 (CD49c), VLA-alpha 5 (CD49e), VLA-alpha 6 (CD49f), intercellular adhesion molecule (ICAM)-3 (CD50), ICAM-1 (CD54), B7 (CD80), and vascular cell adhesion molecule (VCAM)-1 (CD106). With respect to ligands on B cells for these adhesion molecules, the CD11b-CD54, CD50-leukocyte function-associated molecule (LFA)-1 (CD11a/18), and CD106-VLA-4 (CD49d/29) interactions in the apical light (ALZ) and basal light (BLZ) zones; the CD15s-L-selectin (CD62L) and CD106-CD49d/29 interactions in the mantle zone; and the CD54-CD11a/18 interaction in the entire LF may participate in FDC-B cell adhesion. Namely, the adhesion molecules participating in FDC-B cell interactions may differ in each of the five zones. Furthermore, the immunochemical evidence that FDCs were fibronectin (VLA-5, CD49e/29) and laminin (VLA-6, CD49l/29) receptor-positive discussed above was confirmed by immunoelectron microscopy and binding assays. Immunoelectron microscopy revealed fibers surrounded by cytoplasmic FDC extensions that were CD29-, CD49e-, and CD49f-positive. In the binding assays, the numbers of FDCs bound to fibronectin- and laminin-coated dishes and LFs of cryostat sections of human tonsils were reduced markedly by pretreatment with monoclonal antibodies against CD29, CD49e, and CD49f. These data indicate clearly that FDCs bind to reticulin and laminin fibers in LFs via their respective receptors.
分别使用恒冷箱切片和通过磁性细胞分选仪分离的滤泡树突状细胞(FDC)的细胞离心涂片,研究了体内和体外人二级淋巴滤泡(LF)中扁桃体滤泡树突状细胞(FDC)上黏附分子的表达。FDC对Mac-1(CD11b)、唾液酸化路易斯寡糖(CD15s)、CD22、整合素β1(CD29)、CD40、极迟活化抗原(VLA)-α3(CD49c)、VLA-α5(CD49e)、VLA-α6(CD49f)、细胞间黏附分子(ICAM)-3(CD50)、ICAM-1(CD54)、B7(CD80)和血管细胞黏附分子(VCAM)-1(CD106)免疫化学呈阳性。关于B细胞上这些黏附分子的配体,在顶端浅区(ALZ)和基底浅区(BLZ)中,CD11b-CD54、CD50-白细胞功能相关分子(LFA)-1(CD11a/18)以及CD106-VLA-4(CD49d/29)相互作用;在套区中,CD15s-L选择素(CD62L)和CD106-CD49d/29相互作用;在整个LF中,CD54-CD11a/18相互作用可能参与FDC-B细胞黏附。也就是说,参与FDC-B细胞相互作用的黏附分子在五个区域中的每一个区域可能都不同。此外,上述FDC是纤连蛋白(VLA-5,CD49e/29)和层粘连蛋白(VLA-6,CD49l/29)受体阳性的免疫化学证据通过免疫电子显微镜和结合试验得到了证实。免疫电子显微镜显示,纤维被CD29、CD49e和CD49f阳性的FDC细胞质延伸所包围。在结合试验中,用抗CD29、CD49e和CD49f单克隆抗体预处理后,与纤连蛋白和层粘连蛋白包被的培养皿以及人扁桃体恒冷箱切片的LF结合的FDC数量明显减少。这些数据清楚地表明,FDC通过其各自的受体与LF中的网状纤维和层粘连蛋白纤维结合。