Tanaka K, Chen D, Negishi S, Aizawa S, Hoshi H
Department of Anatomy, Nihon University School of Medicine, Tokyo, Japan.
J Anat. 1998 Jul;193 ( Pt 1)(Pt 1):49-59. doi: 10.1046/j.1469-7580.1998.19310049.x.
The reactive formation of lymphoid follicles and germinal centres in lymph nodes, induced by subcutaneous transfer of in vitro activated splenic adherent cells into syngeneic mice, were studied. Adherent cells were obtained by incubating spleen cell suspensions for 24 h and activated by incubating for 1 h in the medium containing keyhole limpet haemocyanin (KLH) absorbed onto alumina. Some of the treated adherent cells were irradiated with 10 Gy x-rays, while others were either not stimulated or were stimulated with alumina-KLH but killed by repeated freezing and thawing. Examination of adherent cell smears immunostained with antibodies against, F4/80, Mac-1, Mac-2 and NLDC-145 indicated that many adherent cells displayed macrophage markers but few displayed the interdigitating cell marker. Animals transfused with KLH-treated adherent cells with or without irradiation showed a marked increase in the number of lymphoid follicles and germinal centres in draining lymph nodes, whereas those transfused with adherent cells which had not been KLH-treated or which had been killed after KLH treatment displayed no significant change in the number of follicles. These results were interpreted as indicating that following transfusion, antigen-activated adherent macrophages migrated into the draining lymph nodes and induced the reactive formation of lymphoid follicles and germinal centres outside preexisting follicles.
研究了通过将体外活化的脾黏附细胞皮下转移至同基因小鼠体内所诱导的淋巴结中淋巴滤泡和生发中心的反应性形成。黏附细胞通过将脾细胞悬液孵育24小时获得,并通过在含有吸附于氧化铝上的钥孔戚血蓝蛋白(KLH)的培养基中孵育1小时进行活化。部分处理后的黏附细胞用10 Gy X射线照射,而其他细胞要么未受刺激,要么用氧化铝-KLH刺激但经反复冻融杀死。用抗F4/80、Mac-1、Mac-2和NLDC-145抗体免疫染色的黏附细胞涂片检查表明,许多黏附细胞显示巨噬细胞标志物,但很少显示树突状细胞标志物。输注经KLH处理的黏附细胞(无论是否照射)的动物,引流淋巴结中淋巴滤泡和生发中心的数量显著增加,而输注未经KLH处理或在KLH处理后已被杀死的黏附细胞的动物,滤泡数量无显著变化。这些结果被解释为表明输血后,抗原活化的黏附巨噬细胞迁移至引流淋巴结,并诱导在预先存在的滤泡外反应性形成淋巴滤泡和生发中心。