肿瘤坏死因子-α对大鼠肺泡上皮细胞紧密连接蛋白ZO-1和Claudin-4表达的影响

Q4 Nursing
石国翠, Shi Guocui, 马申懋, M. Shenmao, 马希刚, M. Xi-gang
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The expression and distribution of tight junction protein ZO-1 and Claudin-4 in each group were observed by immunofluorescence method. The transcriptional levels of ZO-1 and Claudin-4 were detected by real-time fluorescent quantitative PCR. The expressions of ZO-1 and Claudin-4 were detected by Western blot. One-way analysis of variance (ANOVA) was used for comparisons among groups and SNK-q test was used for pairwise comparisons between groups. The non-parametric test of rank transformation was used when homogeneity of variance were not met. The value of P<0.05 was considered significantly different. \n \n \nResults \nTransmission electron microscopy showed that the AEC-Ⅱ cells in the control group obtained characteristic lamellar bodies of different sizes. The lamellar bodies in each TNF-α group were gradually emptied and apoptotic cells were observed under the visual field. 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引用次数: 0

摘要

目的探讨TNF-α对大鼠肺泡上皮Ⅱ型细胞紧密连接蛋白ZO-1和Claudin-4表达的影响。方法体外培养大鼠AEC-Ⅱ细胞,分为对照组和TNF-α24、48、72 h组。对照组用含有胎牛血清的DME F12培养基培养,TNF-α组分别用浓度为10ng/mL的TNF-α干预24小时、48小时和72小时。共培养后,用透射电镜观察大鼠AEC-Ⅱ细胞的超微结构变化。MTT法测定细胞抑制率,流式细胞仪测定细胞凋亡率。免疫荧光法观察各组紧密连接蛋白ZO-1和Claudin-4的表达和分布。实时荧光定量PCR检测ZO-1和Claudin-4的转录水平。免疫印迹法检测ZO-1和Claudin-4的表达。单因素方差分析(ANOVA)用于组间比较,SNK-q检验用于组间配对比较。当不满足方差齐性时,使用秩变换的非参数检验。P<0.05的值被认为有显著差异。结果透射电镜观察,对照组AEC-Ⅱ细胞获得不同大小的具有特征性的片层体。TNF-α组片层体逐渐排空,视野下可见凋亡细胞。各TNF-α组的细胞抑制率和早期凋亡率均显著高于对照组(均P<0.05),而TNF-α48 h组(0.28±0.06)和72 h组(0.13±0.07)的ZO-1 mRNA水平均显著低于对照组。α48 h组(0.44±0.09)和72 h组(0.2±0.01)蛋白水平均低于对照组(0.69±0.12),α组Claudin-4的转录水平(24 h:0.16±0.03;48 h:0.04±0.01;72 h:0.01±0.00 vs 1.00±0.00)和表达(24 h=0.49±0.08;48 h=0.34±0.05;72 h0.04±0.01 vs 0.96±0.13)均显著降低,结论TNF-α可通过损伤肺泡上皮Ⅱ型细胞、下调ZO-1和Claudin-4的表达和分布来破坏肺上皮屏障。关键词:肿瘤坏死因子-α;紧密连接蛋白;急性肺损伤;肺上皮屏障;细胞凋亡
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of tumor necrosis factor-α on the expression of tight junction proteins ZO-1 and Claudin-4 in rat alveolar epithelial cells
Objective To investigate the effect of TNF-α on the expressions of tight junction protein ZO-1 and Claudin-4 in rat alveolar epithelial typeⅡ cells (AEC-Ⅱ). Methods Rat AEC-Ⅱ cells were cultured in vitro and divided into the control group, and TNF-α 24 h, 48 h, 72 h groups. The control group was cultured with DME F12 medium containing fetal bovine serum, and the TNF-α groups were intervened by TNF-α with a concentration of 10 ng/mL for 24 h, 48 h, and 72 h, respectively. After co-culture, the transmission electron microscopy was used to identify and observe the ultrastructural changes of rat AEC-Ⅱ cells. The cell inhibition rate was determined by MTT assay, and the cell apoptosis rate was measured by flow cytometry. The expression and distribution of tight junction protein ZO-1 and Claudin-4 in each group were observed by immunofluorescence method. The transcriptional levels of ZO-1 and Claudin-4 were detected by real-time fluorescent quantitative PCR. The expressions of ZO-1 and Claudin-4 were detected by Western blot. One-way analysis of variance (ANOVA) was used for comparisons among groups and SNK-q test was used for pairwise comparisons between groups. The non-parametric test of rank transformation was used when homogeneity of variance were not met. The value of P<0.05 was considered significantly different. Results Transmission electron microscopy showed that the AEC-Ⅱ cells in the control group obtained characteristic lamellar bodies of different sizes. The lamellar bodies in each TNF-α group were gradually emptied and apoptotic cells were observed under the visual field. The cell inhibition rate and early apoptosis rate of each TNF-α group were significantly higher than those of the control group (all P 0.05). However, the mRNA level of ZO-1 in the TNF-α 48 h group (0.28±0.06) and 72 h group (0.13±0.07) were significantly lower than those in the control group. And their protein levels of TNF-α 48 h group (0.44±0.09) and of TNF-α 72 h group (0.2±0.01) were lower than that of the control group (0.69±0.12). Compared with the control group, the transcription level (24 h: 0.16±0.03; 48 h: 0.04±0.01; 72 h: 0.01±0.00 vs 1.00±0.00) and expression (24 h: 0.49±0.08; 48 h: 0.34±0.05; 72 h: 0.04±0.01 vs 0.96±0.13) of Claudin-4 in each TNF-α group were significantly decreased, and showed a decreasing trend with time (all P<0.05). Conclusions TNF-α can damage the pulmonary epithelial barrier by damaging alveolar epithelial typeⅡ cells and down-regulating the expression and distribution of ZO-1 and Claudin-4. Key words: Tumor necrosis factor-α; Tight junction proteins; Acute lung injury; Pulmonary epithelial barrier; Apoptosis
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来源期刊
中华急诊医学杂志
中华急诊医学杂志 Nursing-Emergency Nursing
CiteScore
0.10
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0.00%
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8629
期刊介绍: Chinese Journal of Emergency Medicine is the only national journal which represents the development of emergency medicine in China. The journal is supervised by China Association of Science and Technology, sponsored by Chinese Medical Association, and co-sponsored by Zhejiang University. The journal publishes original research articles dealing with all aspects of clinical practice and research in emergency medicine. The columns include Pre-Hospital Rescue, Emergency Care, Trauma, Resuscitation, Poisoning, Disaster Medicine, Continuing Education, etc. It has a wide coverage in China, and builds up communication with Hong Kong, Macao, Taiwan and international emergency medicine circles.
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