Denis V, Dupuis P, Bizouarne N, de O Sampaio S, Hong L, Lebret M, Monsigny M, Nakache M, Kieda C
Centre de Biophysique Moléculaire, Centre National de la Recherche Scientifique and Université d'Orléans, France.
J Leukoc Biol. 1996 Dec;60(6):744-52. doi: 10.1002/jlb.60.6.744.
Vascular endothelial cell addressins play an important role in lymphocyte homing in secondary lymphoid organs and in chronic inflammatory areas. A SV40 large T antigen-immortalized cell line from peripheral lymph nodes, HECa1O [Bizouarne et al., 1993a], was used to characterize the location of addressins with regard to environmental factors and cytokines. For this purpose, two monoclonal antibodies, MECA 79 and MECA 367, specific for peripheral lymph node vascular addressin and for mucosal addressin (Peyer's patches), respectively, were bound to unstimulated HECa1O cells. Both mucosal and peripheral addressins were detected inside the cells and in cellular extracts of the resting cells. On the cell surface, both addressins could be evidenced on the same cells at a moderate level of expression. They partly mediate the EL4/EL4IL2 lymphoma cells' adhesion to HECa1O cells. Supernatants of cultured peripheral lymph node or Peyers' patch cells induced expression of MECA 79 or MECA 367 antigens, respectively, on the surface of HECa1O cells. Interleukins, IL-7, IL-3, and IL-8, induced the cell-surface appearance of MECA 79 but not of MECA 367 antigen. Therefore, the same cell type synthesizes both antigens, but the expression of these antigens on the cell surface is independently regulated, thus uncovering a characteristic tissue type-specific as well as environment-sensitive properties of microvascular endothelial cells.
血管内皮细胞地址素在淋巴细胞归巢至二级淋巴器官以及慢性炎症区域中发挥着重要作用。利用一株源自外周淋巴结的经SV40大T抗原永生化的细胞系HECa1O[比祖阿内等人,1993年a],来表征地址素相对于环境因素和细胞因子的定位。为此,将两种分别针对外周淋巴结血管地址素和黏膜地址素(派伊尔结)的单克隆抗体MECA 79和MECA 367与未受刺激的HECa1O细胞结合。在静息细胞的细胞内和细胞提取物中均检测到了黏膜地址素和外周地址素。在细胞表面,两种地址素在同一细胞上均有适度表达。它们部分介导了EL4/EL4IL2淋巴瘤细胞与HECa1O细胞的黏附。培养的外周淋巴结或派伊尔结细胞的上清液分别诱导了HECa1O细胞表面MECA 79或MECA 367抗原的表达。白细胞介素IL-7、IL-3和IL-8诱导了MECA 79在细胞表面的出现,但未诱导MECA 367抗原的出现。因此,同一细胞类型合成两种抗原,但这些抗原在细胞表面的表达是独立调节的,从而揭示了微血管内皮细胞具有特征性的组织类型特异性以及环境敏感性特性。