Blum Katrin S, Pabst Reinhard
Department of Functional and Applied Anatomy, Hannover Medical School, Germany.
J Anat. 2006 Nov;209(5):585-95. doi: 10.1111/j.1469-7580.2006.00650.x.
New molecular markers are constantly increasing our knowledge of developmental processes. In this review article we have attempted to summarize the keystones of lymphoid tissue development in embryonic and pathological conditions. During embryonic lymph node development in the mouse, cells from the anterior cardinal vein start to bud and sprout, forming a lymph sac at defined sites. The protrusion of mesenchymal tissue into the lymph sacs forms the environment, where so-called 'lymphoid tissue inducer cells' and 'mesenchymal organizer cells' meet and interact. Defects of molecules involved in the recruitment and signalling cascades of these cells lead to primary immunodeficiency diseases. A comparison of molecules involved in the development of secondary lymphoid organs and tertiary lymphoid organs, e.g. in autoimmune diseases, shows that the same molecules are involved in both processes. This has led to the hypothesis that the development of tertiary lymphoid organs is a recapitulation of embryonic lymphoid tissue development at ectopic sites.
新的分子标志物不断增进我们对发育过程的了解。在这篇综述文章中,我们试图总结胚胎期和病理状态下淋巴组织发育的关键要点。在小鼠胚胎期淋巴结发育过程中,来自前主静脉的细胞开始出芽并萌发,在特定部位形成淋巴囊。间充质组织突入淋巴囊形成一个环境,所谓的“淋巴组织诱导细胞”和“间充质组织者细胞”在这个环境中相遇并相互作用。参与这些细胞募集和信号级联反应的分子缺陷会导致原发性免疫缺陷疾病。对参与二级淋巴器官和三级淋巴器官发育的分子进行比较,例如在自身免疫性疾病中,结果表明这两个过程涉及相同的分子。这就产生了一个假说,即三级淋巴器官的发育是异位部位胚胎淋巴组织发育的重演。