Institute of Neuropathology, University of Zurich, Zurich, Switzerland.
Eur J Immunol. 2010 Aug;40(8):2134-8. doi: 10.1002/eji.201040765.
In 1965, Mitchell and Abbot (Mitchell, J. and Abbot A, Nature 1965. 30: 500-502) discovered peculiar cells with filiform processes, which were capable of capturing and retaining antigens within secondary lymphoid organs. Yet half a century since the first description of follicular dendritic cells (FDC), their function and their histogenesis remain largely mysterious. FDC are thought to help with organization of the lymphoid follicles, to facilitate the germinal center reaction by presenting antigen to B cells, and to legislate the engulfment of apoptotic bodies, but it has proved difficult to stringently verify any of these functions. One reason for such slow progress is a dearth of markers specific to FDC and their precursors, which limits our ability to isolate, target, and follow FDC. Here we review the current state of FDC science with specific reference to a study in this issue of the European Journal of Immunology and its efforts in discovering new FDC markers.
1965 年,Mitchell 和 Abbot(Mitchell,J. 和 Abbot A,自然 1965. 30: 500-502)发现了具有丝状突起的特殊细胞,这些细胞能够在次级淋巴器官中捕获和保留抗原。然而,自滤泡树突状细胞(FDC)的首次描述以来已经过去了半个世纪,它们的功能和组织发生仍然很大程度上是神秘的。FDC 被认为有助于淋巴滤泡的组织,通过向 B 细胞呈递抗原来促进生发中心反应,并规定对凋亡小体的吞噬作用,但事实证明很难严格验证这些功能中的任何一种。进展如此缓慢的一个原因是缺乏 FDC 及其前体特异性的标记物,这限制了我们分离、靶向和跟踪 FDC 的能力。在这里,我们回顾了 FDC 科学的现状,特别提到了本期《欧洲免疫学杂志》中的一项研究及其在发现新的 FDC 标记物方面的努力。