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嗜酸性粒细胞趋化因子是CCR2的天然拮抗剂和CCR5的激动剂。

Eotaxin is a natural antagonist for CCR2 and an agonist for CCR5.

作者信息

Ogilvie P, Bardi G, Clark-Lewis I, Baggiolini M, Uguccioni M

机构信息

Institute for Research in Biomedicine, Bellinzona, Switzerland.

出版信息

Blood. 2001 Apr 1;97(7):1920-4. doi: 10.1182/blood.v97.7.1920.

Abstract

Eotaxin is a potent inducer of eosinophil chemotaxis and was considered as a selective ligand of the CC chemokine receptor 3 (CCR3), which is expressed on eosinophils, basophils, and Th2 lymphocytes. This study shows that eotaxin also interacts with CCR2 and CCR5 and can, thus, affect the responses of monocytes, which express both receptors. In human monocytes pretreatment with eotaxin decreased responsiveness to MCP-1, a selective ligand for CCR2, as well as to RANTES and MIP-1 beta, which bind to CCR5. Similar effects were obtained with transfected cells expressing CCR2 or CCR5, but here a difference became apparent: Eotaxin triggered CCR5 at a concentration of 100 nM but not CCR2 even at 1 microM, suggesting an antagonistic effect on this receptor. In agreement with this observation, eotaxin induced internalization of CCR5 but not of CCR2 in human monocytes and transfected cells. Binding studies showed that eotaxin displaces (125) I-MCP-1 from monocytes in a concentration-dependent manner, and functional experiments showed that eotaxin inhibits MCP-1-induced chemotaxis and enzyme release. The results demonstrate that eotaxin is a CCR5 agonist and a CCR2 antagonist. The present findings suggest a role of eotaxin in the fine-tuning of cellular responses occurring at sites of allergic inflammation, in which both MCP-1 and eotaxin are produced. (Blood. 2001;97:1920-1924)

摘要

嗜酸性粒细胞趋化因子是嗜酸性粒细胞趋化作用的强效诱导剂,曾被认为是CC趋化因子受体3(CCR3)的选择性配体,CCR3在嗜酸性粒细胞、嗜碱性粒细胞和Th2淋巴细胞上表达。本研究表明,嗜酸性粒细胞趋化因子还可与CCR2和CCR5相互作用,因此能够影响同时表达这两种受体的单核细胞的反应。在人类单核细胞中,用嗜酸性粒细胞趋化因子预处理会降低其对CCR2的选择性配体MCP-1以及与CCR5结合的RANTES和MIP-1β的反应性。用表达CCR2或CCR5的转染细胞也得到了类似的结果,但在此出现了一个明显的差异:嗜酸性粒细胞趋化因子在浓度为100 nM时可激活CCR5,但即使在1 μM时也不能激活CCR2,提示其对该受体具有拮抗作用。与这一观察结果一致,嗜酸性粒细胞趋化因子可诱导人类单核细胞和转染细胞中CCR5的内化,但不能诱导CCR2的内化。结合研究表明,嗜酸性粒细胞趋化因子以浓度依赖的方式从单核细胞中置换出(125)I-MCP-1,功能实验表明,嗜酸性粒细胞趋化因子可抑制MCP-1诱导的趋化作用和酶释放。结果表明,嗜酸性粒细胞趋化因子是一种CCR5激动剂和CCR2拮抗剂。目前的研究结果提示,嗜酸性粒细胞趋化因子在过敏性炎症部位发生的细胞反应的精细调节中发挥作用,在这些部位,MCP-1和嗜酸性粒细胞趋化因子均会产生。(《血液》。2001年;97:1920 - 1924)

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