Willführ K U, Westermann J, Pabst R
Center of Anatomy 4150, Medical School of Hannover, FRG.
Eur J Immunol. 1990 Apr;20(4):903-11. doi: 10.1002/eji.1830200428.
Lymphocyte migration is one of the basic principles of the immune system. Up to now lymphocyte migration experiments have been performed either in a quantitative way, determining whole organ recoveries of radiolabeled lymphocytes without histologic localization, or based on autoradiography which does not provide absolute numbers of immigrant lymphocytes. In this study the traffic of lymphocyte subsets through the splenic compartments: red pulp (RP), marginal zone (MZ), periarteriolar lymphatic sheath (PALS) and follicle was evaluated in absolute numbers. In normal spleens and splenic transplants fluorescein isothiocyanate (FITC)-labeled immigrant lymphocytes were localized and characterized immunohistochemically in cryostat sections by light microscopy. In addition morphometry of the splenic compartments was performed and the recovery of 51Cr-labeled lymphocytes in the spleen was determined. The combination of these methods allowed total numbers of immigrant subset cells to be calculated in individual splenic compartments. At 15 min about 17% of the injected B lymphocytes were found in the MZ. This is the largest fraction of an injected lymphocyte subset found in a single splenic compartment. At 24 h immigrant B cells were not only found in the follicle, but they had reached comparable numbers in the three compartments: follicle, RP and MZ. Most immigrant T lymphocytes were found in the PALS, which from 6 h after injection onwards contained more T cell immigrants than any single organ of the body. CD4+ and CD8+ lymphocytes showed a similar distribution throughout the splenic compartments at early time points. At 24 h CD4+ lymphocytes homed preferentially to the PALS, whereas CD8+ cells seemed to prefer the RP and MZ. Both CD4+ and CD8+ cells also migrated into the follicles. In regenerated splenic tissue after autotransplantation lymphocyte immigration was reduced in all compartments and to the MZ in particular. An impaired lymphocyte migration to the MZ in splenic transplants may be one reason for the lack of protection provided against bacterial infections. Thus examining lymphocyte migration in absolute numbers provides additional information which cannot be gained by determining labeling indices or percentages of lymphocyte subsets alone.
淋巴细胞迁移是免疫系统的基本原理之一。到目前为止,淋巴细胞迁移实验要么是以定量方式进行,测定放射性标记淋巴细胞的全器官回收率而不进行组织学定位,要么基于放射自显影术,而该方法无法提供迁移淋巴细胞的绝对数量。在本研究中,以绝对数量评估了淋巴细胞亚群通过脾区室的运输情况,这些脾区室包括红髓(RP)、边缘区(MZ)、动脉周围淋巴鞘(PALS)和滤泡。在正常脾脏和脾移植中,用异硫氰酸荧光素(FITC)标记的迁移淋巴细胞通过免疫组织化学在低温切片中进行定位和鉴定,通过光学显微镜观察。此外,对脾区室进行形态测量,并测定51Cr标记淋巴细胞在脾脏中的回收率。这些方法的结合使得能够计算出各个脾区室中迁移亚群细胞的总数。在15分钟时,约17%注入的B淋巴细胞出现在边缘区。这是在单个脾区室中发现的注入淋巴细胞亚群的最大比例。在24小时时,迁移的B细胞不仅出现在滤泡中,而且在三个区室(滤泡、红髓和边缘区)中数量相当。大多数迁移的T淋巴细胞出现在动脉周围淋巴鞘中,从注射后6小时起,该区域所含的T细胞迁移数量比身体的任何单个器官都多。在早期时间点,CD4+和CD8+淋巴细胞在整个脾区室中的分布相似。在24小时时,CD4+淋巴细胞优先归巢至动脉周围淋巴鞘,而CD8+细胞似乎更倾向于红髓和边缘区。CD4+和CD8+细胞也都迁移至滤泡。自体移植后再生的脾组织中,所有区室的淋巴细胞迁移均减少,尤其是边缘区。脾移植中淋巴细胞向边缘区迁移受损可能是缺乏针对细菌感染的保护作用的原因之一。因此,以绝对数量检查淋巴细胞迁移可提供单独测定淋巴细胞亚群的标记指数或百分比无法获得的额外信息。