Ohbayashi M, Ito M, Nakayama A, Kasai K, Asai J
Department of Pathology, Nagoya University School of Medicine, Japan.
Virchows Arch B Cell Pathol Incl Mol Pathol. 1993;63(5):297-306. doi: 10.1007/BF02899276.
The distribution of high endothelial venules (HEVs) in various rat organs has been investigated immunohistochemically using two monoclonal antibodies (MoAbs), REC16-11 and REC4-1. The staining patterns observed with REC16-11 and REC4-1 were compared with those obtained with the MoAb anti-rat ICAM-1, which is a cell adhesion molecule in HEVs. REC16-11 reacted not only with HEVs but also with all vascular endothelial cells (ECs) in the tissues examined. Electronmicroscopy showed that REC16-11 and REC4-1 reacted with the cell surface antigens of ECs and immunoblot analysis of rat splenic stromal preparations showed that REC4-1 stained 42 kd and 60 kd bands. REC4-1 inhibited the binding of lymphocyte to HEVs in the mucosa-associated lymphoid tissues (MALT), but had no effects on lymphocyte binding to HEVs in peripheral (non-mucosal) lymph nodes. These findings suggested that the MoAb REC4-1 recognized the associated antigen of the lymphocyte-HEV recognition system in MALT.
利用两种单克隆抗体(MoAb)REC16 - 11和REC4 - 1,通过免疫组织化学方法研究了高内皮微静脉(HEV)在各种大鼠器官中的分布。将用REC16 - 11和REC4 - 1观察到的染色模式与用抗大鼠ICAM - 1单克隆抗体获得的染色模式进行比较,抗大鼠ICAM - 1是HEV中的一种细胞粘附分子。REC16 - 11不仅与HEV反应,还与所检查组织中的所有血管内皮细胞(EC)反应。电子显微镜显示REC16 - 11和REC4 - 1与EC的细胞表面抗原反应,对大鼠脾脏基质制剂的免疫印迹分析表明REC4 - 1染出了42kd和60kd的条带。REC4 - 1抑制淋巴细胞与黏膜相关淋巴组织(MALT)中HEV的结合,但对淋巴细胞与外周(非黏膜)淋巴结中HEV的结合没有影响。这些发现表明单克隆抗体REC4 - 1识别MALT中淋巴细胞 - HEV识别系统的相关抗原。