基础研究

PM2.5 对支气管上皮细胞色素上皮衍生因子表达的影响①

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  • 1. 南京医科大学第二附属医院呼吸科,江苏南京市210011;2. 南京医科大学第二临床医学院,江苏南京市210011。

网络出版日期: 2016-12-05

Effects of PM2.5 on Expression of Pigment Epithelium-derived Factor in Bronchial Epithelial Cells

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  • 1. Department of Respiration Medicine, No.2 Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210011, China; 2. the Second Clinical Medical School of Nanjing Medical University, Nanjing, Jiangsu 210011, China

Online published: 2016-12-05

摘要

目的探索不同浓度PM2.5 对支气管上皮细胞(BEAS-2B)色素上皮衍生因子(PEDF)蛋白表达的影响。方法BEAS-2B细胞传代培养,加入低、中、高浓度PM2.5 悬液(25 μg/ml、50 μg/ml、100 μg/ml)刺激24 h。采用酶联免疫吸附试验(ELISA)检测细胞培养上清液中PEDF 水平;Western blotting 检测BEAS-2B细胞中PEDF 蛋白表达水平。结果与对照组相比,PM2.5 浓度为25μg/ml 时,细胞内和上清液中PEDF蛋白水平均有增加趋势,但无统计学意义(t=-0.730, t=-1.840, P>0.05);PM2.5 浓度为50 μg/ml和100 μg/ml 时,细胞内和上清液中PEDF蛋白表达水平明显增高(t>5.798, P<0.01)。结论中、高浓度PM2.5 能够增加支气管上皮细胞中PEDF蛋白水平,并呈浓度依赖性。

本文引用格式

朱成华1,2,施丽君2,张灵凤2,计晓兰2,杜强1,2 . PM2.5 对支气管上皮细胞色素上皮衍生因子表达的影响①[J]. 中国康复理论与实践, 2016 , 22(10) : 1151 -1153 . DOI: 10.3969/j.issn.1006-9771.2016.10.008

Abstract

Objective To explore the effect of particulate matter (PM) 2.5 on the expression of pigment epithelium- derived factor (PEDF) protein in bronchial epithelial cells (BEAS-2B). Methods Human BEAS-2B were subcultivated, followed by low, medium and high concentrations of PM2.5 (25 μg/ml, 50 μg/ml, 100 μg/ml) stimulation for 24 hours. The expression of PEDF protein in supernatant was analyzed by enzyme-linked immunosorbent assay (ELISA), and the expression in BEAS-2B cells was detected by Western blotting. Results Compared with the control group, the expression of PEDF protein in supernatant and BEAS-2B cells induced by PM2.5 (25 μg/ml) increased, but no significance was found (t=-0.730, t=-1.840, P>0.05), and the expression induced by PM2.5 with the concentrations of 50 μg/ml and 100 μg/ml significantly increased (t>5.798, P<0.05). Conclusion PM2.5 with the concentrations of 50 μg/ml and 100 μg/ml could increase the expression of PEDF protein in a concentration-dependent manner both in supernatant and BEAS-2B cells.
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