Centenary Institute and AW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, University of Sydney, Sydney, Australia.
J Hepatol. 2012 Aug;57(2):352-8. doi: 10.1016/j.jhep.2012.03.023. Epub 2012 Apr 25.
BACKGROUND & AIMS: Lymph nodes (LNs) play a critical role in host defence against pathogens. In rodents, lymphatic anatomy and drainage have been characterized for many different organs. Surprisingly, the LNs draining the mouse liver have not been clearly identified. This knowledge is of central importance to allow accurate characterization of immune responses to pathogens infecting the liver. It is also important for exploring immune responses in hepatic tumour models, and mechanisms underlying the relative tolerogenic properties of the liver. In this study, we used both anatomical and immunological approaches to identify the LN(s) draining the mouse liver.
Evans Blue and purified dendritic cells were directly injected into the hepatic parenchyma.
Using Evans Blue, we identified three LNs adjacent to the liver that stained with the dye within the first 5 min, which we termed portal, coeliac, and first mesenteric LNs. We also provide evidence that dendritic cells (DCs) injected under the liver capsule preferentially migrate to the coeliac and portal nodes, leading to local activation of antigen-specific naïve CD8 and CD4 T cells, suggesting this is a route of lymphatic drainage from the liver. Consistent with this result, cell-associated antigen injected under the liver capsule was also cross-presented to CD8 T cells in these nodes.
These results suggest for the first time that the coeliac and portal nodes are the main LNs draining the liver, and that DCs exiting the liver can elicit primary T cell activation within these lymph nodes; first mesenteric nodes play a secondary role. We propose this nomenclature to be used as common designations for the observed structures.
淋巴结(LNs)在宿主防御病原体方面起着至关重要的作用。在啮齿动物中,已经对许多不同器官的淋巴解剖结构和引流进行了描述。令人惊讶的是,尚不清楚引流小鼠肝脏的 LNs。这些知识对于准确描述感染肝脏的病原体引起的免疫反应至关重要。对于研究肝肿瘤模型中的免疫反应以及肝脏相对耐受特性的机制也很重要。在这项研究中,我们使用解剖学和免疫学方法来确定引流小鼠肝脏的 LN。
直接将 Evans Blue 和纯化的树突状细胞注射到肝实质中。
使用 Evans Blue,我们鉴定出三个紧邻肝脏的 LN,在最初的 5 分钟内用染料染色,我们将其称为门脉、腹腔和第一肠系膜 LN。我们还提供了证据表明,注射到肝包膜下的树突状细胞(DCs)优先迁移到腹腔和门脉节点,导致抗原特异性初始 CD8 和 CD4 T 细胞的局部激活,这表明这是肝脏的淋巴引流途径。与该结果一致,注射到肝包膜下的细胞相关抗原也在这些节点中交叉呈递给 CD8 T 细胞。
这些结果首次表明,腹腔和门脉节点是引流肝脏的主要 LN,并且离开肝脏的 DC 可以在这些淋巴结中引发初始 T 细胞激活;第一肠系膜节点起次要作用。我们建议使用这种命名法作为观察到的结构的通用名称。