Farone A L, Frevert C W, Farone M B, Morin M J, Fields B N, Paulauskis J D, Kobzik L
Department of Environmental Health, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
J Virol. 1996 Oct;70(10):7079-84. doi: 10.1128/JVI.70.10.7079-7084.1996.
Reovirus type 3 Dearing (T3D) causes a prominent neutrophil influx, substantially greater than seen with reovirus type 1 Lang (T1L) in a rat model of viral pneumonia. We sought to measure reovirus-mediated increases in chemokine mRNA expression in pulmonary cells. We found that the neutrophilia induced by T1L and T3D infection in vivo correlated directly with increased levels of chemokine mRNA expression in T3D-infected compared with those of T1IL-infected lungs. In vitro, reovirus-infected normal alveolar macrophages (AMs) and the rat AM cell line NR8383 expressed greater levels of macrophage inflammatory protein 2, KC, and tumor necrosis factor alpha mRNA. A synergism between reovirus and lipopolysaccharide was also detected for macrophage inflammatory protein 2 and KC mRNA expression. Tumor necrosis factor protein secretion was also increased to a greater extent by T3D than by T1L in primary rat AMs and the NR8383 cells. We conclude that the virus-mediated inflammatory cytokine induction suggests a role for these cytokines in the neutrophil influx observed in the rat reovirus pneumonia model.
3型迪林呼肠孤病毒(T3D)会引起显著的中性粒细胞浸润,在病毒性肺炎大鼠模型中,这种浸润程度比1型朗氏呼肠孤病毒(T1L)引起的要大得多。我们试图测量呼肠孤病毒介导的肺细胞趋化因子mRNA表达的增加。我们发现,在体内,T1L和T3D感染诱导的中性粒细胞增多与T3D感染的肺相比T1L感染的肺中趋化因子mRNA表达水平的增加直接相关。在体外,呼肠孤病毒感染的正常肺泡巨噬细胞(AM)和大鼠AM细胞系NR8383表达更高水平的巨噬细胞炎性蛋白2、KC和肿瘤坏死因子α mRNA。对于巨噬细胞炎性蛋白2和KC mRNA表达,还检测到呼肠孤病毒与脂多糖之间的协同作用。在原代大鼠AM和NR8383细胞中,T3D比T1L更能显著增加肿瘤坏死因子蛋白的分泌。我们得出结论,病毒介导的炎性细胞因子诱导表明这些细胞因子在大鼠呼肠孤病毒肺炎模型中观察到的中性粒细胞浸润中起作用。