Ozeki Yuriko, Tsutsui Hiroko, Kawada Norifumi, Suzuki Hiroshi, Kataoka Motoyuki, Kodama Tatsuhiko, Yano Ikuya, Kaneda Kenji, Kobayashi Kazuo
Department of Host Defense, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan.
Microb Pathog. 2006 Apr;40(4):171-6. doi: 10.1016/j.micpath.2005.12.006. Epub 2006 Mar 6.
We aimed to reveal the regulatory function of macrophage scavenger receptor-A (MSR-A) in proinflammatory cytokine production by macrophages stimulated with mycobacterial cord factor (CF). By the culture with CF, MSR-A (+/+) alveolar macrophages and Kupffer cells produced TNF-alpha/MIP-1alpha in a time- and dose-dependent manner. However, the amounts of cytokines produced by them were much less compared to those produced by MSR-A (-/-) macrophages. Consistent with this, treatment of MSR-A (+/+) macrophages with anti-MSR-A antibody increased TNF-alpha production. Binding of CF to MSR-A was demonstrated by measuring the binding affinity. These results indicate that CF binds MSR-A, and MSR-A down-regulates TNF-alpha/MIP-1alpha production by activated macrophages, suggesting the role of this receptor in suppression of excessive inflammatory responses during mycobacterial infection.
我们旨在揭示巨噬细胞清道夫受体-A(MSR-A)在经分枝杆菌索状因子(CF)刺激的巨噬细胞促炎细胞因子产生中的调节功能。通过与CF共培养,MSR-A(+/+)肺泡巨噬细胞和库普弗细胞以时间和剂量依赖性方式产生肿瘤坏死因子-α/巨噬细胞炎性蛋白-1α。然而,与MSR-A(-/-)巨噬细胞产生的细胞因子量相比,它们产生的细胞因子量要少得多。与此一致的是,用抗MSR-A抗体处理MSR-A(+/+)巨噬细胞会增加肿瘤坏死因子-α的产生。通过测量结合亲和力证明了CF与MSR-A的结合。这些结果表明CF与MSR-A结合,并且MSR-A下调活化巨噬细胞产生肿瘤坏死因子-α/巨噬细胞炎性蛋白-1α,提示该受体在分枝杆菌感染期间抑制过度炎症反应中的作用。