Kang W, Nielsen O, Fenger C, Madsen J, Hansen S, Tornoe I, Eggleton P, Reid K B M, Holmskov U
MRC Immunochemistry Unit, Department of Biochemistry, Oxford University, Oxford, UK.
Clin Exp Immunol. 2002 Dec;130(3):449-58. doi: 10.1046/j.1365-2249.2002.01992.x.
Gp-340 is a glycoprotein belonging to the scavenger receptor cysteine rich (SRCR) group B family. It binds to host immune components such as lung surfactant protein D (SP-D). Recent studies found that gp-340 interacts directly with pathogenic microorganisms and induces their aggregation, suggesting its involvement in innate immunity. In order to investigate further its potential immune functions in the appropriate cell lines, the expression of gp-340 in four conventional immune cell lines (U937, HL60, Jurkat, Raji), and two innate immune-related epithelial cell lines (A549 derived from lung and AGS from stomach), was examined by RT-PCR and immunohistochemistry. The resting immune cell lines showed weak or no gp-340 mRNA expression; while the two epithelial cell lines expressed gp-340 at much higher level, which was differentially regulated by phorbol myristate acetate (PMA) treatment. In the A549 cells, gp-340 was up-regulated along with the PMA-induced proinflammatory expression of both IL-6 and IL-8. In AGS cells, PMA down-regulation of gp-340 was seen in parallel with an up-regulation of the two mature gastric epithelial specific proteins TFF1 (trefoil factor 1) and TFF2, which are implicated as markers of terminal differentiation. Analysis of the distribution of gp-340, together with the TFFs and SP-D in normal lung and gastric mucosa, supported further our in vitro data. We conclude that the differential regulation of gp-340 in the two epithelial cell lines by PMA indicates that gp-340 s involvement in mucosal defence and growth of epithelial cells may vary at different body locations and during different stages of epithelial differentiation.
Gp - 340是一种属于富含半胱氨酸清道夫受体(SRCR)B族的糖蛋白。它能与宿主免疫成分如肺表面活性蛋白D(SP - D)结合。最近的研究发现,gp - 340与致病微生物直接相互作用并诱导其聚集,表明它参与先天免疫。为了在合适的细胞系中进一步研究其潜在的免疫功能,通过逆转录聚合酶链反应(RT - PCR)和免疫组织化学检测了gp - 340在四种传统免疫细胞系(U937、HL60、Jurkat、Raji)以及两种与先天免疫相关的上皮细胞系(源自肺的A549和源自胃的AGS)中的表达。静息免疫细胞系显示出微弱或无gp - 340 mRNA表达;而两种上皮细胞系中gp - 340表达水平高得多,并受到佛波酯(PMA)处理的差异调节。在A549细胞中,gp - 340随着PMA诱导的白细胞介素 - 6(IL - 6)和白细胞介素 - 8(IL - 8)促炎表达而上调。在AGS细胞中,可以看到PMA使gp - s40下调,同时两种成熟的胃上皮特异性蛋白三叶因子1(TFF1)和三叶因子2(TFF2)上调,这两种蛋白被认为是终末分化的标志物。对正常肺和胃黏膜中gp - 340以及TFF和SP - D分布的分析进一步支持了我们的体外数据。我们得出结论:PMA对两种上皮细胞系中gp - 340表达进行差异调节,这表明gp - 340在黏膜防御和上皮细胞生长中的作用可能在不同身体部位以及上皮分化的不同阶段有所不同。