Jones M L, Mulligan M S, Flory C M, Ward P A, Warren J S
Department of Pathology, University of Michigan Medical School, Ann Arbor 48109-0602.
J Immunol. 1992 Sep 15;149(6):2147-54.
We have examined the role of monocyte chemoattractant protein 1 (MCP 1) in the pathogenesis of monocyte/macrophage-dependent IgA immune complex alveolitis in the rat. Rat MCP 1 was cloned and expressed in order to facilitate analysis of its function in rat models of human disease. A cDNA library was constructed from rat pulmonary artery endothelial cells stimulated with TNF-alpha. The cDNA library was screened with synthetic oligonucleotide probes based on the recently published rat MCP 1 cDNA sequence. Among numerous MCP 1-positive clones, four full length (approximately 480 bp) cDNA were rescued, amplified by polymerase chain reaction, and ligated into a pJVETLZ baculovirus transfer vector. Spodoptera frugiperda insect cells (Sf-21) infected with baculovirus recombinants (Auto-grapha california nuclear polyhedrosis virus) bearing properly oriented MCP 1 cDNA (AcMCP 1) directed the expression of unique peptides of 18, 21, and 23 kDa. Treatment of AcMCP 1-infected Sf-21 cells with tunicamycin resulted in reduced production of the 21- and 23-kDa proteins and an increase in 16- to 18-kDa products, the predicted size range of uncleaved and nonglycosylated rat MCP 1. Denatured and refolded 23-kDa and 21-kDa rat MCP 1 species exhibited dose-dependent monocyte-specific chemotactic activity at concentrations as low as 10(-10) M whereas the 18-kDa species exhibited negligible activity. Antibodies that react with the immunoblot, block rat rMCP 1-directed monocyte chemotaxis, and neutralize monocyte-specific chemotactic activity secreted by TNF-stimulated rat endothelial cells were raised in rabbits immunized with the 23-kDa MCP 1 species. Intravenous administration of anti-MCP 1 antibodies upon initiation of IgA immune complex lung injury resulted in a marked reduction in lung injury as measured by pulmonary vascular permeability, alveolar hemorrhage, and pulmonary monocyte/macrophage recruitment and pulmonary monocyte/macrophage recruitment. These data suggest that MCP 1 may play an important role in the pathogenesis of monocyte/macrophage-dependent IgA immune complex alveolitis in the rat.
我们研究了单核细胞趋化蛋白1(MCP - 1)在大鼠单核细胞/巨噬细胞依赖性IgA免疫复合物肺泡炎发病机制中的作用。克隆并表达大鼠MCP - 1,以便于分析其在人类疾病大鼠模型中的功能。用肿瘤坏死因子 - α刺激的大鼠肺动脉内皮细胞构建cDNA文库。基于最近发表的大鼠MCP - 1 cDNA序列,用合成寡核苷酸探针筛选该cDNA文库。在众多MCP - 1阳性克隆中,拯救出四个全长(约480 bp)的cDNA,通过聚合酶链反应扩增,并连接到pJVETLZ杆状病毒转移载体中。用携带正确定向的MCP - 1 cDNA(AcMCP - 1)的杆状病毒重组体(苜蓿银纹夜蛾核型多角体病毒)感染草地贪夜蛾昆虫细胞(Sf - 21),可指导表达18、21和23 kDa的独特肽段。用衣霉素处理感染AcMCP - 1的Sf - 21细胞,导致21 kDa和23 kDa蛋白产量降低,16至18 kDa产物增加,这是未切割和未糖基化大鼠MCP - 1的预测大小范围。变性并复性的23 kDa和21 kDa大鼠MCP - 1物种在低至10(-10)M的浓度下表现出剂量依赖性的单核细胞特异性趋化活性,而18 kDa物种的活性可忽略不计。用23 kDa MCP - 1物种免疫兔子,产生了与免疫印迹反应、阻断大鼠rMCP - 1介导的单核细胞趋化作用并中和肿瘤坏死因子刺激的大鼠内皮细胞分泌的单核细胞特异性趋化活性的抗体。在IgA免疫复合物肺损伤开始时静脉注射抗MCP - 1抗体,通过肺血管通透性、肺泡出血以及肺单核细胞/巨噬细胞募集来衡量,肺损伤明显减轻。这些数据表明,MCP - 1可能在大鼠单核细胞/巨噬细胞依赖性IgA免疫复合物肺泡炎的发病机制中起重要作用。