Rovin B H, Yoshiumura T, Tan L
Department of Medicine, Ohio State University, Columbus 43210.
J Immunol. 1992 Apr 1;148(7):2148-53.
The infiltration of the glomerulus by monocyte-derived macrophages is an important step in the pathogenesis of glomerular injury. The factors regulating glomerular leukocyte traffic remain unknown. We postulated that the glomerular mesangial cell (MC) may participate in the development of glomerular inflammation through the production of the monocyte-specific chemotactic factor, monocyte chemoattractant protein-1 (MCP-1). Using a cell culture system, we found that human MC produced a basal level of monocyte chemotactic activity, which was significantly increased by the inflammatory cytokines IL-1 beta and TNF-alpha. This increase in bioactivity correlated with the increased expression of MCP-1 mRNA by cytokine-conditioned MC. The total chemotactic activity of MC-conditioned supernatants was reduced by more than 80% after immunoadsorption with a specific anti-MCP-1 antibody. Thus, MC could play a role in inflammatory glomerular conditions through the production of MCP-1.
单核细胞衍生的巨噬细胞浸润肾小球是肾小球损伤发病机制中的重要一步。调节肾小球白细胞运输的因素尚不清楚。我们推测肾小球系膜细胞(MC)可能通过产生单核细胞特异性趋化因子——单核细胞趋化蛋白-1(MCP-1)参与肾小球炎症的发展。利用细胞培养系统,我们发现人MC产生基础水平的单核细胞趋化活性,炎性细胞因子IL-1β和TNF-α可使其显著增加。这种生物活性的增加与细胞因子处理后的MC中MCP-1 mRNA表达增加相关。用特异性抗MCP-1抗体进行免疫吸附后,MC条件培养液的总趋化活性降低了80%以上。因此,MC可能通过产生MCP-1在炎性肾小球疾病中发挥作用。