Ohl Lars, Mohaupt Mariette, Czeloth Niklas, Hintzen Gabriele, Kiafard Ziba, Zwirner Jörg, Blankenstein Thomas, Henning Golo, Förster Reinhold
Institute of Immunology, Hannover Medical School, 30625 Hannover, Germany.
Immunity. 2004 Aug;21(2):279-88. doi: 10.1016/j.immuni.2004.06.014.
The CC chemokine receptor CCR7 has been identified as a key regulator of homeostatic B and T cell trafficking to secondary lymphoid organs. Data presented here demonstrate that CCR7 is also an essential mediator for entry of both dermal and epidermal dendritic cells (DC) into the lymphatic vessels within the dermis while this receptor is dispensable for the mobilization of Langerhans cells from the epidermis to the dermis. Moreover, a distinct population of CD11c(+)MHCII(high) DC showing low expression of the costimulatory molecules CD40, CD80, and CD86 in wild-type animals was virtually absent in skin-draining lymph nodes of CCR7-deficient mice under steady-state conditions. We provide evidence that these cells represent a semimature population of DC that is capable of initiating T cell proliferation under conditions known to induce tolerance. Thus, our data identify CCR7 as a key regulator that governs trafficking of skin DC under both inflammatory and steady-state conditions.
CC趋化因子受体CCR7已被确定为稳态B细胞和T细胞向次级淋巴器官迁移的关键调节因子。本文提供的数据表明,CCR7也是真皮和表皮树突状细胞(DC)进入真皮内淋巴管的重要介质,而该受体对于朗格汉斯细胞从表皮迁移至真皮并非必需。此外,在稳态条件下,CCR7缺陷小鼠的皮肤引流淋巴结中几乎不存在野生型动物体内那种表达共刺激分子CD40、CD80和CD86水平较低的独特CD11c(+)MHCII(高)DC群体。我们提供的证据表明,这些细胞代表了一种半成熟的DC群体,在已知诱导耐受的条件下能够启动T细胞增殖。因此,我们的数据确定CCR7是在炎症和稳态条件下控制皮肤DC迁移的关键调节因子。