Abernethy N J, Hay J B, Kimpton W G, Washington E, Cahill R N
Department of Pathology, University of Toronto, Ontario, Canada.
Immunology. 1991 Feb;72(2):239-45.
Tissue-specific and lymphocyte subset-specific lymphocyte recirculation patterns have been analysed simultaneously. Lymphocytes obtained from one lymph compartment were directly labelled with fluorochrome in vitro and returned to the blood of the same animal. Over the next 48-72 h, the recirculation of these cells into both the same lymph compartment and at least one different lymph compartment was monitored. The cells in all of these lymph collections, as well as an aliquot of the cells used for direct fluorescent labelling, were then phenotyped with monoclonal antibodies (mAb) which define the mutually exclusive small CD4+ and CD8+ T-lymphocyte subsets in sheep. All cell samples were analysed by flow cytometry and CD4/CD8 ratios were determined for the recirculated, fluorochrome-labelled population in each lymph collection. The mean CD4/CD8 ratio calculated for each lymph compartment was then compared with the CD4/CD8 ratio calculated for each lymph compartment was then compared with the CD4/CD8 ratio of the transfused, starting population. In one experiment employing efferent prescapular lymph cells, three experiments employing efferent intestinal lymph cells, and two experiments employing afferent intestinal lymph cells, tissue-specific recirculation was observed. In all of these experiments, the pattern of recirculation of small CD4+ and CD8+ T lymphocytes was non-random. Moreover, in each experiment, this non-randomness was completely unrelated to tissue-specific phenomena, since the mean CD4/CD8 ratio of the recirculated population was higher than the CD4/CD8 ratio of the transfused, starting population regardless of the lymph compartment examined. These data are therefore consistent with the hypothesis that tissue-specific and lymphocyte subset-specific lymphocyte-endothelial cell recognition mechanisms independently direct the recirculation of small lymphocytes from blood to lymph.
同时分析了组织特异性和淋巴细胞亚群特异性的淋巴细胞再循环模式。从一个淋巴腔室获取的淋巴细胞在体外直接用荧光染料标记,然后回输到同一动物的血液中。在接下来的48 - 72小时内,监测这些细胞再循环到同一淋巴腔室以及至少一个不同淋巴腔室的情况。然后,使用单克隆抗体(mAb)对所有这些淋巴收集物中的细胞以及用于直接荧光标记的一部分细胞进行表型分析,这些单克隆抗体可区分绵羊中相互排斥的小CD4 +和CD8 + T淋巴细胞亚群。通过流式细胞术分析所有细胞样本,并确定每个淋巴收集物中再循环的、荧光染料标记的群体的CD4/CD8比率。然后将为每个淋巴腔室计算的平均CD4/CD8比率与为每个淋巴腔室计算的CD4/CD8比率进行比较,再与输注的起始群体的CD4/CD8比率进行比较。在一项使用肩胛前输出淋巴细胞的实验、三项使用肠输出淋巴细胞的实验以及两项使用肠输入淋巴细胞的实验中,均观察到了组织特异性再循环。在所有这些实验中,小CD4 +和CD8 + T淋巴细胞的再循环模式是非随机的。此外,在每个实验中,这种非随机性与组织特异性现象完全无关,因为无论检查的是哪个淋巴腔室,再循环群体的平均CD4/CD8比率都高于输注的起始群体的CD4/CD8比率。因此,这些数据与以下假设一致,即组织特异性和淋巴细胞亚群特异性的淋巴细胞 - 内皮细胞识别机制独立地指导小淋巴细胞从血液到淋巴的再循环。