Department of Immunology, The Weizmann Institute of Science, Rehovot, Israel.
Immunity. 2012 Dec 14;37(6):1076-90. doi: 10.1016/j.immuni.2012.08.026. Epub 2012 Dec 6.
Ly6C(hi) monocytes seed the healthy intestinal lamina propria to give rise to resident CX(3)CR1(+) macrophages that contribute to the maintenance of gut homeostasis. Here we report on two alternative monocyte fates in the inflamed colon. We showed that CCR2 expression is essential to the recruitment of Ly6C(hi) monocytes to the inflamed gut to become the dominant mononuclear cell type in the lamina propria during settings of acute colitis. In the inflammatory microenvironment, monocytes upregulated TLR2 and NOD2, rendering them responsive to bacterial products to become proinflammatory effector cells. Ablation of Ly6C(hi) monocytes ameliorated acute gut inflammation. With time, monocytes differentiated into migratory antigen-presenting cells capable of priming naive T cells, thus acquiring hallmarks reminiscent of dendritic cells. Collectively, our results highlight cellular dynamics in the inflamed colon and the plasticity of Ly6C(hi) monocytes, marking them as potential targets for inflammatory bowel disease (IBD) therapy.
Ly6C(hi) 单核细胞在健康的肠道固有层中定殖,产生常驻的 CX(3)CR1(+)巨噬细胞,有助于维持肠道内稳态。在这里,我们报告了在炎症结肠中两种替代的单核细胞命运。我们表明,CCR2 表达对于 Ly6C(hi)单核细胞向炎症肠道的募集至关重要,在急性结肠炎的情况下,它们成为固有层中主要的单核细胞类型。在炎症微环境中,单核细胞上调 TLR2 和 NOD2,使其对细菌产物产生反应,成为促炎效应细胞。清除 Ly6C(hi)单核细胞可改善急性肠道炎症。随着时间的推移,单核细胞分化为具有迁移能力的抗原呈递细胞,能够激活幼稚 T 细胞,从而获得类似于树突状细胞的特征。总之,我们的研究结果强调了炎症结肠中的细胞动力学和 Ly6C(hi)单核细胞的可塑性,将其标记为炎症性肠病 (IBD) 治疗的潜在靶点。