Berger J T, Voynow J A, Peters K W, Rose M C
Center for Molecular Mechanisms of Diseases, Children's Research Institute, Children's National Medical Center, Washington, DC 20010-2970, USA.
Am J Respir Cell Mol Biol. 1999 Mar;20(3):500-10. doi: 10.1165/ajrcmb.20.3.3383.
Lung carcinoma cell lines are being used in many laboratories to study various airway epithelial functions, including mucin gene expression. To identify model systems for investigating regulation of MUC5/5AC gene expression and secretion of MUC5/5AC mucins in airway epithelial cells, we evaluated the expression of several mucin genes in six carcinoma cell lines of respiratory tract origin. RNA was extracted from A549, Calu-3, NCI H292, Calu-6, RPMI 2650, and A-427 cells; MUC1, MUC2, MUC4, MUC5/5AC, and MUC5B messenger RNA (mRNA) expression was determined. By Northern analyses, all cell lines expressed MUC1 mRNA, whereas MUC2 mRNA was not detectable in any of the cell lines. RPMI 2650 cell lines expressed only MUC1 mRNA. NCI-H292 cells expressed MUC4 and low levels of MUC5/5AC mRNA. Calu-3 and A549 cells expressed MUC5/5AC mRNA; A549 cells also expressed MUC5B mRNA. Glycoconjugates secreted by lung carcinoma cells were also examined. By wheat germ lectin analysis, Calu-3, H292, and A549 cells secreted high molecular weight glycoproteins having N-acetylglucosamine and/or sialic acid moieties. Western blot analyses with an anti-MUC5:TR-3A antibody demonstrated that Calu-3 and A549 cells secreted MUC5/5AC mucins. All six carcinoma cell lines secreted large, radiolabeled, sulfated macromolecules; the majority were proteoglycans that were digested by hyaluronidase. However, Calu-3 cells also secreted sulfated high molecular-weight glycoproteins that were immunoprecipitated by anti-MUC5:TR-3A antibody. These studies demonstrated that Calu-3 and A549 cell lines expressed high and moderate amounts of MUC5/5AC mRNA and MUC5/5AC mucins, whereas H292 cells expressed lesser amounts. These cell lines should prove useful for studies of MUC5/5AC gene expression and MUC5/5AC biosynthesis, trafficking, and secretions in airway epithelial cells.
许多实验室正在使用肺癌细胞系来研究各种气道上皮功能,包括粘蛋白基因表达。为了确定用于研究气道上皮细胞中MUC5/5AC基因表达调控和MUC5/5AC粘蛋白分泌的模型系统,我们评估了六种呼吸道来源的癌细胞系中几种粘蛋白基因的表达。从A549、Calu-3、NCI H292、Calu-6、RPMI 2650和A-427细胞中提取RNA;测定MUC1、MUC2、MUC4、MUC5/5AC和MUC5B信使核糖核酸(mRNA)的表达。通过Northern分析,所有细胞系均表达MUC1 mRNA,而在任何细胞系中均未检测到MUC2 mRNA。RPMI 2650细胞系仅表达MUC1 mRNA。NCI-H292细胞表达MUC4和低水平的MUC5/5AC mRNA。Calu-3和A549细胞表达MUC5/5AC mRNA;A549细胞还表达MUC5B mRNA。还检测了肺癌细胞分泌的糖缀合物。通过麦胚凝集素分析,Calu-3、H292和A549细胞分泌具有N-乙酰葡糖胺和/或唾液酸部分的高分子量糖蛋白。用抗MUC5:TR-3A抗体进行的蛋白质印迹分析表明,Calu-3和A549细胞分泌MUC5/5AC粘蛋白。所有六种癌细胞系均分泌大量放射性标记的硫酸化大分子;大多数是被透明质酸酶消化的蛋白聚糖。然而,Calu-3细胞还分泌被抗MUC5:TR-3A抗体免疫沉淀的硫酸化高分子量糖蛋白。这些研究表明,Calu-3和A549细胞系表达高水平和中等水平的MUC5/5AC mRNA和MUC5/5AC粘蛋白,而H292细胞表达量较少。这些细胞系对于研究气道上皮细胞中MUC5/5AC基因表达以及MUC5/5AC生物合成、运输和分泌应该是有用的。