Pabst Oliver, Herbrand Heike, Worbs Tim, Friedrichsen Michaela, Yan Sheng, Hoffmann Matthias W, Körner Heiner, Bernhardt Günter, Pabst Reinhard, Förster Reinhold
Institute of Immunology, Hannover Medical School, D-30625 Hannover, Germany.
Eur J Immunol. 2005 Jan;35(1):98-107. doi: 10.1002/eji.200425432.
In comparison to secondary lymphoid organs, gut-associated lymphoid tissues such as isolated lymphoid follicles (ILF) and cryptopatches (CP) have been less intensively studied. To gain a better insight into processes regulating organization and function of these structures, which are believed to participate in immune responses and extrathymic T cell development, we characterized the lymphoid structures of the murine small intestine in more detail. The size and cellular composition of small intestinal lymphoid aggregations were analyzed in C57BL/6 and BALB/c wild-type and lymphotoxin (LT)-deficient mice, by flow cytometry, histology and automated multi-color immunofluorescence microscopy evaluating large coherent areas of the intestine. These evaluations demonstrate that aggregated lymphoid structures in the small intestine vary in size and cellular composition, with a majority of structures not matching the current definitions of CP or ILF. Accordingly, significant variations depending on species, age and mouse strain were observed. Furthermore, small bowel transplantation revealed a rapid exchange of B but not T cells between host and grafted tissue. Moreover, LT-deficient animals lack any intestinal lymphoid aggregations yet possess the complete panel of intraepithelial lymphocytes (IEL). In summary, our observations disclose intestinal lymphoid aggregations as dynamic structures with a great deal of inborn plasticity and demonstrate their dispensability for the generation of IEL.
与次级淋巴器官相比,肠道相关淋巴组织,如孤立淋巴滤泡(ILF)和隐窝斑(CP),受到的研究较少。为了更深入了解调节这些结构的组织和功能的过程,这些结构被认为参与免疫反应和胸腺外T细胞发育,我们更详细地描述了小鼠小肠的淋巴结构。通过流式细胞术、组织学和自动多色免疫荧光显微镜对C57BL/6和BALB/c野生型及淋巴毒素(LT)缺陷小鼠的小肠淋巴聚集物的大小和细胞组成进行了分析,评估了肠道的大片连贯区域。这些评估表明,小肠中的聚集淋巴结构在大小和细胞组成上各不相同,大多数结构不符合目前对CP或ILF的定义。因此,观察到了因物种、年龄和小鼠品系而异的显著差异。此外,小肠移植显示宿主和移植组织之间B细胞能快速交换,但T细胞不能。此外,LT缺陷动物缺乏任何肠道淋巴聚集物,但拥有完整的上皮内淋巴细胞(IEL)群。总之,我们的观察结果揭示肠道淋巴聚集物是具有很大先天性可塑性的动态结构,并证明它们对于IEL的产生并非必不可少。