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EBI1/CCR7是树突状细胞趋化因子受体的一个新成员,在成熟时上调。

EBI1/CCR7 is a new member of dendritic cell chemokine receptor that is up-regulated upon maturation.

作者信息

Yanagihara S, Komura E, Nagafune J, Watarai H, Yamaguchi Y

机构信息

Pharmaceutical Research Laboratory, Kirin Brewery Co., Ltd., Takasaki, Gunma, Japan.

出版信息

J Immunol. 1998 Sep 15;161(6):3096-102.

PMID:9743376
Abstract

Dendritic cells (DC) that are stimulated with inflammatory mediators can maturate and migrate from nonlymphoid tissues to lymphoid organs to initiate T cell-mediated immune responses. This migratory step is closely related to the maturation of the DC. In an attempt to identify chemokine receptors that might influence migration and are selectively expressed in mature DC, we have discovered that the chemokine receptor, EBI1/CCR7, is strikingly up-regulated upon maturation in three distinct culture systems: 1) mouse bone marrow-derived DC, 2) mouse epidermal Langerhans cells, and 3) human monocyte-derived DC. The EBI1/CCR7 expressed in mature DC is functional because ELC/MIP-3beta, recently identified as a ligand of EBI1/CCR7, induces a rise in intracellular free calcium concentrations and directional migration of human monocyte-derived mature DC (HLA-DRhigh, CD1a(low), CD14-, CD25+, CD83+, and CD86high) in a dose-dependent manner, but not of immature DC (HLA-DRlow, CD1a(high), CD14-, CD25-, CD83-, and CD86-). In contrast, macrophage inflammatory protein-1alpha (MIP-1alpha), monocyte chemotactic protein-3 (MCP-3), and RANTES are active on immature DC but not on mature DC. Thus, it seems likely that MIP-1alpha, MCP-3, and RANTES can mediate the migration of immature DC located in peripheral sites, whereas ELC/MIP-3beta can direct the migration of Ag-carrying DC from peripheral inflammatory sites, where DC are stimulated to up-regulate the expression of EBI1/CCR7, to lymphoid organs. It is postulated that different chemokines and chemokine receptors are involved in DC migration in vivo, depending on the maturation state of DC.

摘要

受到炎症介质刺激的树突状细胞(DC)能够成熟,并从非淋巴组织迁移至淋巴器官,从而启动T细胞介导的免疫反应。这一迁移步骤与DC的成熟密切相关。为了确定可能影响迁移并在成熟DC中选择性表达的趋化因子受体,我们发现在三种不同的培养体系中,趋化因子受体EBI1/CCR7在成熟时显著上调:1)小鼠骨髓来源的DC;2)小鼠表皮朗格汉斯细胞;3)人单核细胞来源的DC。成熟DC中表达的EBI1/CCR7具有功能,因为最近被确定为EBI1/CCR7配体的ELC/MIP-3β能以剂量依赖的方式诱导人单核细胞来源的成熟DC(HLA-DR高、CD1a低、CD14-、CD25+、CD83+和CD86高)细胞内游离钙浓度升高和定向迁移,但对未成熟DC(HLA-DR低、CD1a高、CD14-、CD25-、CD83-和CD86-)无此作用。相反,巨噬细胞炎性蛋白-1α(MIP-1α)、单核细胞趋化蛋白-3(MCP-3)和RANTES对未成熟DC有活性,但对成熟DC无活性。因此,MIP-1α、MCP-3和RANTES似乎可以介导位于外周部位的未成熟DC的迁移,而ELC/MIP-3β可以引导携带抗原的DC从外周炎症部位迁移至淋巴器官,在外周炎症部位DC被刺激上调EBI1/CCR7的表达。据推测,在体内DC迁移过程中,根据DC的成熟状态,不同的趋化因子和趋化因子受体参与其中。

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