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CC 趋化因子受体 2(CCR2)和甲酰肽受体 2(Fpr2)在招募过敏性气道炎症中的单核细胞衍生树突状细胞中的信号转导作用。

Signal relay by CC chemokine receptor 2 (CCR2) and formylpeptide receptor 2 (Fpr2) in the recruitment of monocyte-derived dendritic cells in allergic airway inflammation.

机构信息

Laboratory of Molecular Immunoregulation, Cancer and Inflammation Program, Center for Cancer Research.

SAIC-Frederick, Frederick, Maryland 21702.

出版信息

J Biol Chem. 2013 Jun 7;288(23):16262-16273. doi: 10.1074/jbc.M113.450635. Epub 2013 Apr 19.

Abstract

Chemoattractant receptors regulate leukocyte accumulation at sites of inflammation. In allergic airway inflammation, although a chemokine receptor CCR2 was implicated in mediating monocyte-derived dendritic cell (DC) recruitment into the lung, we previously also discovered reduced accumulation of DCs in the inflamed lung in mice deficient in formylpeptide receptor Fpr2 (Fpr2(-/-)). We therefore investigated the role of Fpr2 in the trafficking of monocyte-derived DCs in allergic airway inflammation in cooperation with CCR2. We report that in allergic airway inflammation, CCR2 mediated the recruitment of monocyte-derived DCs to the perivascular region, and Fpr2 was required for further migration of the cells into the bronchiolar area. We additionally found that the bronchoalveolar lavage liquid from mice with airway inflammation contained both the CCR2 ligand CCL2 and an Fpr2 agonist CRAMP. Furthermore, similar to Fpr2(-/-) mice, in the inflamed airway of CRAMP(-/-) mice, DC trafficking into the peribronchiolar areas was diminished. Our study demonstrates that the interaction of CCR2 and Fpr2 with their endogenous ligands sequentially mediates the trafficking of DCs within the inflamed lung.

摘要

趋化因子受体调节炎症部位白细胞的聚集。在过敏性气道炎症中,虽然趋化因子受体 CCR2 被认为介导单核细胞衍生的树突状细胞(DC)募集到肺部,但我们之前还发现,在缺乏甲酰肽受体 Fpr2(Fpr2(-/-))的小鼠中,DC 在肺部炎症部位的聚集减少。因此,我们研究了 Fpr2 在与 CCR2 合作的过敏性气道炎症中单核细胞衍生的 DC 迁移中的作用。我们报告说,在过敏性气道炎症中,CCR2 介导单核细胞衍生的 DC 募集到血管周围区域,而 Fpr2 则是细胞进一步迁移到细支气管区域所必需的。我们还发现,来自气道炎症小鼠的支气管肺泡灌洗液中含有 CCR2 配体 CCL2 和 Fpr2 激动剂 CRAMP。此外,与 Fpr2(-/-) 小鼠相似,在 CRAMP(-/-) 小鼠的炎症气道中,DC 向细支气管周围区域的迁移减少。我们的研究表明,CCR2 和 Fpr2 与其内源性配体的相互作用依次介导了 DC 在肺部炎症中的迁移。

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