Kimura M
Immunology. 1983 Jun;49(2):223-9.
Ultrastructural localization of immunoglobulin G (IgG) in the postcapillary venules (PVC) of normal and nude mouse lymph nodes was examined in thin sections which had been stained sequentially with primary exposure to biotin-conjugated goat anti-mouse IgG serum and a secondary immersion in a ferritin-linked avidin (IF). In the normal mouse PCV, reaction products showing IgG-binding sites were detected as large IF clusters on the luminal membrane of the endothelial cells, as small IF clusters in the intercellular spaces between the endothelial cells and some migrating lymphocytes, and as uniform precipitates of large numbers of IF particles in the basement membrane. By contrast, nude mouse PCV retained a few or almost no IgG-binding sites in portions comparable to those observed in the normal mouse. A relatively large number of plasma cells in the lymphoid stroma of both strains possessed large IF clusters on the cell surfaces. The significance of the IgG localization in the PCV of the two strains is discussed in relation to the mechanism of lymphocyte recirculation.
在正常小鼠和裸鼠淋巴结的毛细血管后微静脉(PVC)中,通过依次用生物素偶联的山羊抗小鼠IgG血清进行初次染色,然后用铁蛋白连接的抗生物素蛋白(IF)进行二次浸染的薄切片,对免疫球蛋白G(IgG)进行超微结构定位研究。在正常小鼠的PVC中,显示IgG结合位点的反应产物在内皮细胞的腔膜上被检测为大的IF簇,在内皮细胞与一些迁移淋巴细胞之间的细胞间隙中为小的IF簇,在基底膜中为大量IF颗粒的均匀沉淀物。相比之下,裸鼠的PVC在与正常小鼠中观察到的部分相当的部位保留了很少或几乎没有IgG结合位点。两种品系的淋巴组织基质中相对大量的浆细胞在细胞表面具有大的IF簇。结合淋巴细胞再循环机制讨论了两种品系PVC中IgG定位的意义。