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小鼠C-C趋化因子JE和FIC受体mCCR2的克隆与功能表达

Cloning and functional expression of mCCR2, a murine receptor for the C-C chemokines JE and FIC.

作者信息

Kurihara T, Bravo R

机构信息

Department of Oncology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543-4000, USA.

出版信息

J Biol Chem. 1996 May 17;271(20):11603-7. doi: 10.1074/jbc.271.20.11603.

Abstract

The C-C chemokines human monocyte chemoattractant protein-1 and -3 (MCP-1 and MCP-3) and mouse JE and FIC are potent activators of monocytes. Several receptors for MCP-1 and MCP-3 have been cloned from human monocytic cell lines, and one of these receptors, CCR2B, binds both MCP-l and MCP-3. Thus far, no murine receptors for JE or FIC have been reported. We have cloned a novel murine C-C chemokine receptor, designated mouse CCR2 (mCCR2), from the mouse monocyte cell line WEHI265.1. The predicted 373-amino acid sequence of mCCR2 shows highest identity (80%) with CCR2B. When stably expressed in human embryonic kidney 293 cells, mCCR2 specifically bound 125I-JE with high affinity. FIC was less potent than JE in competing 125I-JE binding to mCCR2-expressing cells, while three other mouse chemokines, MIP-1alpha, C10, and N51/KC, did not compete. mccr2 mRNA expression was detected in elicited peritoneal macrophages as well as in several mouse organs. The cloning of mCCR2 provides an important tool to investigate monocyte/macrophage responses to JE and FIC, to identify other targets for their action, and potentially to study models of CCR2 function in the mouse.

摘要

C-C趋化因子人类单核细胞趋化蛋白-1和-3(MCP-1和MCP-3)以及小鼠JE和FIC是单核细胞的有效激活剂。已从人类单核细胞系中克隆出几种MCP-1和MCP-3的受体,其中一种受体CCR2B能结合MCP-1和MCP-3。到目前为止,尚未报道JE或FIC的鼠类受体。我们从小鼠单核细胞系WEHI265.1中克隆了一种新的鼠类C-C趋化因子受体,命名为小鼠CCR2(mCCR2)。预测的mCCR2的373个氨基酸序列与CCR2B的同源性最高(80%)。当在人胚肾293细胞中稳定表达时,mCCR2能以高亲和力特异性结合125I-JE。在与125I-JE竞争结合表达mCCR2的细胞方面,FIC的效力低于JE,而其他三种小鼠趋化因子MIP-1α、C10和N51/KC则无竞争作用。在诱导的腹腔巨噬细胞以及几个小鼠器官中检测到了mccr2 mRNA的表达。mCCR2的克隆为研究单核细胞/巨噬细胞对JE和FIC的反应、确定它们作用的其他靶点以及潜在地研究小鼠中CCR2功能的模型提供了一个重要工具。

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