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人巨噬细胞炎性蛋白1α/调节激活正常T细胞表达和分泌因子受体的结构与功能表达

Structure and functional expression of the human macrophage inflammatory protein 1 alpha/RANTES receptor.

作者信息

Gao J L, Kuhns D B, Tiffany H L, McDermott D, Li X, Francke U, Murphy P M

机构信息

Laboratory of Host Defenses, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Exp Med. 1993 May 1;177(5):1421-7. doi: 10.1084/jem.177.5.1421.

Abstract

The chemokine beta family is comprised of at least six distinct cytokines that regulate trafficking of phagocytes and lymphocytes in mammalian species; at least one of these, macrophage inflammatory protein 1 alpha (MIP-1 alpha), also regulates the growth of hematopoietic stem cells. We now show that MIP-1 alpha and the related beta chemokine, RANTES, induce transient alterations in intracellular Ca2+ concentration in polymorphonuclear leukocytes that can be reciprocally and specifically desensitized, suggesting a common receptor. Moreover, we have now cloned both the cDNA and the gene for this receptor, functionally expressed the receptor in Xenopus oocytes, and mapped the gene to human chromosome 3p21. Transcripts for the receptor were found in mature and immature myeloid cells as well as B cells. The receptor is a member of the G protein-coupled receptor superfamily. It has approximately 33% amino acid identity with receptors for the alpha chemokine, interleukin 8, and may be the human homologue of the product of US28, an open reading frame of human cytomegalovirus.

摘要

趋化因子β家族由至少六种不同的细胞因子组成,这些细胞因子调节哺乳动物物种中吞噬细胞和淋巴细胞的运输;其中至少有一种,即巨噬细胞炎性蛋白1α(MIP-1α),也调节造血干细胞的生长。我们现在表明,MIP-1α和相关的β趋化因子RANTES可诱导多形核白细胞内细胞内Ca2+浓度的短暂变化,这种变化可以相互且特异性地脱敏,提示存在共同受体。此外,我们现已克隆了该受体的cDNA和基因,在非洲爪蟾卵母细胞中功能性表达了该受体,并将该基因定位到人类染色体3p21。在成熟和未成熟的髓样细胞以及B细胞中发现了该受体的转录本。该受体是G蛋白偶联受体超家族的成员。它与α趋化因子白细胞介素8的受体具有约33%的氨基酸同一性,可能是人类巨细胞病毒开放阅读框US28产物的人类同源物。

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