Regulation and Functional Involvement of Macrophage Scavenger Receptor MARCO in Clearance of Bacteria In Vivo

清道夫受体 巨噬细胞 吞噬作用 促炎细胞因子 受体 体内 微生物学 生物 免疫系统 脾脏 受体表达 肿瘤坏死因子α 肠系膜淋巴结 分子生物学 免疫学 炎症 体外 生物化学 生物技术 脂蛋白 胆固醇
作者
Luc J. W. van der Laan,Ed A. Döpp,Richard Haworth,Timo Pikkarainen,Maarit Kangas,Outi Elomaa,Christine D. Dijkstra,Siamon Gordon,Karl Tryggvason,Georg Kraal
出处
期刊:Journal of Immunology [American Association of Immunologists]
卷期号:162 (2): 939-947 被引量:281
标识
DOI:10.4049/jimmunol.162.2.939
摘要

The scavenger receptors expressed by macrophages are thought to play an important role in the immune response against bacteria by mediating binding and phagocytosis. A novel member of the class A scavenger receptor family, macrophage receptor with collagenous structure (MARCO), has recently been identified. In this study we have generated a panel of mAbs with specificities for different domains of this receptor. Two of those reacting with the C-terminal cysteine-rich domain block ligand binding of MARCO. The in vivo expression of this murine receptor is normally restricted to distinct populations of macrophages in the spleen and lymph nodes. During bacillus Calmette-Guérin (BCG) infection, during bacterial sepsis, or after the injection of purified LPS, however, the expression of MARCO is rapidly induced on macrophages in other tissues, including Kupffer cells in the liver. Using the mouse macrophage cell line J774.2, it was shown that LPS stimulation up-regulates surface expression of MARCO in a dose- and time-dependent fashion. The proinflammatory cytokines IL-1, IL-6, TNF-alpha, and IFN-gamma had little or no effect. Using inhibitory mAbs, the relevance of MARCO for the clearance of circulating bacteria in vivo was determined. Although the overall elimination of live Escherichia coli and Staphylococcus aureus from the blood did not appear to be affected by treatment with these Abs, the capturing of heat-killed bacteria by macrophages in the marginal zone areas of the spleen was clearly inhibited. This study suggests a role for MARCO in the host antibacterial defense.
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