Meier Dominik, Bornmann Caroline, Chappaz Stephane, Schmutz Sandrine, Otten Luc A, Ceredig Rhodri, Acha-Orbea Hans, Finke Daniela
Division of Developmental Immunology, Center for Biomedicine, Department of Clinical and Biological Sciences (DKBW), University of Basel, CH-4058 Basel, Switzerland.
Immunity. 2007 May;26(5):643-54. doi: 10.1016/j.immuni.2007.04.009.
Development of Peyer's patches and lymph nodes requires the interaction between CD4+ CD3- IL-7Ralpha+ lymphoid-tissue inducer (LTi) and VCAM-1+ organizer cells. Here we showed that by promoting their survival, enhanced expression of interleukin-7 (IL-7) in transgenic mice resulted in accumulation of LTi cells. With increased IL-7 availability, de novo formation of VCAM-1+ Peyer's patch anlagen occurred along the entire fetal gut resulting in a 5-fold increase in Peyer's patch numbers. IL-7 overexpression also led to formation of multiple organized ectopic lymph nodes and cecal patches. After immunization, ectopic lymph nodes developed normal T cell-dependent B cell responses and germinal centers. Mice overexpressing IL-7 but lacking either RORgamma, a factor required for LTi cell generation, or lymphotoxin alpha1beta2 had neither Peyer's patches nor ectopic lymph nodes. Therefore, by controlling LTi cell numbers, IL-7 can regulate the formation of both normal and ectopic lymphoid organs.
派尔集合淋巴结和淋巴结的发育需要CD4+ CD3- IL-7Rα+淋巴组织诱导细胞(LTi)与VCAM-1+组织细胞之间的相互作用。我们在此表明,通过促进其存活,转基因小鼠中白细胞介素-7(IL-7)表达增强导致LTi细胞积累。随着IL-7可利用性增加,沿整个胎儿肠道从头形成VCAM-1+派尔集合淋巴结原基,导致派尔集合淋巴结数量增加5倍。IL-7过表达还导致形成多个有组织的异位淋巴结和盲肠小结。免疫后,异位淋巴结产生正常的T细胞依赖性B细胞反应和生发中心。过表达IL-7但缺乏LTi细胞生成所需因子RORγ或淋巴毒素α1β2的小鼠既没有派尔集合淋巴结也没有异位淋巴结。因此,通过控制LTi细胞数量,IL-7可以调节正常和异位淋巴器官的形成。