Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Center for Immunology and Inflammatory Diseases, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Immunity. 2018 Sep 18;49(3):449-463.e6. doi: 10.1016/j.immuni.2018.07.012. Epub 2018 Aug 28.
The migration of mature dendritic cells (DCs) into the draining lymph node (dLN) is thought to depend solely on the chemokine receptor CCR7. CD301b DCs migrate into the dLN after cutaneous allergen exposure and are required for T helper 2 (Th2) differentiation. We found that CD301b DCs poorly upregulated CCR7 expression after allergen exposure and required a second chemokine signal, mediated by CCR8 on CD301b DCs and its ligand CCL8, to exit the subcapsular sinus (SCS) and enter the lymph node (LN) parenchyma. After allergen exposure, CD169SIGN-R1 macrophages in interfollicular regions produced CCL8, which synergized with CCL21 in a Src-kinase-dependent manner to promote CD301b DC migration. In CCR8-deficient mice, CD301b DCs remained in the SCS and were unable to enter the LN parenchyma, resulting in defective Th2 differentiation. We have defined a CCR8-dependent stepwise mechanism of DC-subset-specific migration through which LN CD169SIGN-R1 macrophages control the polarization of the adaptive immune response.
成熟树突状细胞(DCs)迁移到引流淋巴结(dLN)被认为仅依赖于趋化因子受体 CCR7。在皮肤过敏原暴露后,CD301b DC 迁移到 dLN,是 T 辅助 2(Th2)分化所必需的。我们发现,CD301b DC 在过敏原暴露后 CCR7 表达上调不佳,需要第二个趋化因子信号,由 CD301b DC 上的 CCR8 和其配体 CCL8 介导,以离开被膜下窦(SCS)并进入淋巴结(LN)实质。在过敏原暴露后,滤泡间区域的 CD169SIGN-R1 巨噬细胞产生 CCL8,它与 CCL21 协同作用,以 Src 激酶依赖性方式促进 CD301b DC 迁移。在 CCR8 缺陷小鼠中,CD301b DC 仍留在 SCS 中,无法进入 LN 实质,导致 Th2 分化缺陷。我们已经定义了一个 CCR8 依赖性的 DC 亚群特异性迁移分步机制,通过该机制,LN CD169SIGN-R1 巨噬细胞控制适应性免疫反应的极化。