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MCP-1基因敲除、CCR-2基因敲除或双基因敲除小鼠大脑中脑膜巨噬细胞和血管周围巨噬细胞的更新

Turn-over of meningeal and perivascular macrophages in the brain of MCP-1-, CCR-2- or double knockout mice.

作者信息

Schilling Matthias, Strecker Jan-Kolja, Ringelstein E Bernd, Kiefer Reinhard, Schäbitz Wolf-Rüdiger

机构信息

Department of Neurology, University Hospital Münster, Münster, Germany.

出版信息

Exp Neurol. 2009 Oct;219(2):583-5. doi: 10.1016/j.expneurol.2009.07.003. Epub 2009 Jul 15.

DOI:10.1016/j.expneurol.2009.07.003
PMID:19615366
Abstract

Perivascular and meningeal macrophages are important for immune surveillance in the healthy and the injured brain. Monocyte chemoattractant protein-1 (MCP-1) regulates macrophage migration and permeability of the blood brain barrier. In the present study, we investigated the influence of MCP-1 or/and chemokine receptor 2 (CCR2)-deficiency on macrophage turnover. The results showed no influence of single MCP-1- or CCR-2-deficiency, but double-deficient mice revealed a virtual absence of blood-borne macrophage recruitment. This finding emphasizes that the MCP-1/CCR2 axis is crucially important for macrophage turnover and compensatory mechanisms remain only partially sufficient to sustain regulatory functions.

摘要

血管周围和脑膜巨噬细胞对健康及损伤大脑中的免疫监视至关重要。单核细胞趋化蛋白-1(MCP-1)调节巨噬细胞迁移及血脑屏障的通透性。在本研究中,我们调查了MCP-1或/和趋化因子受体2(CCR2)缺陷对巨噬细胞更新的影响。结果显示,单一MCP-1或CCR-2缺陷并无影响,但双缺陷小鼠显示几乎没有血源巨噬细胞募集。这一发现强调,MCP-1/CCR2轴对巨噬细胞更新至关重要,且代偿机制仅部分足以维持调节功能。

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