[长期暴露于石棉诱导的人间皮细胞中 miRNAs 和 EMT 相关基因的表达变化]。

Q3 Medicine
R Li, W K Yu, Q Wang, L J Zhu, F F Zhang
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引用次数: 0

摘要

研究目的研究长期暴露于温石棉和青石棉对人胸膜间皮细胞中 miRNAs 和上皮间充质转化(EMT)相关基因表达的影响。研究方法2020年11月,采用荧光定量聚合酶链反应(RT-qPCR)检测人胸膜间皮瘤细胞(NCl-H2052细胞、NCl-H2452细胞)和人正常间皮细胞(Met-5A细胞)中EMT相关基因的表达。从研究组以往的 miRNA 芯片数据中筛选出在人胸膜间皮瘤细胞中异常表达的 miRNA,并利用 miRWalk 数据库(http://mirwalk.umm.uni-heidelberg.de)预测了差异表达 miRNA 的靶基因。采用 RT-qPCR 验证细胞系中 EMT 相关 miRNA 的异常表达。分别用 5μg/cm(2) 温石棉和青石棉处理 Met-5A 细胞,每次 48 小时,每周一次,共 10 次。分别设置温石棉组、青石棉组和对照组。对照组加入相同体积的 PBS。采用 RT-qPCR 法检测各组 EMT 相关基因和异常表达 miRNA 的表达变化。各组间差异比较采用单因素方差分析,对照组与实验组间差异比较采用dunnet-t检验。结果与 Met-5A 细胞相比,NCl-H2052 细胞和 NCl-H2452 细胞中 Vimentin 和 Twist 基因的表达水平升高,E-cadherin 基因的表达水平降低(PPPPConclusion:长期暴露于温石棉和青石棉可导致Met-5A细胞产生与间皮瘤细胞相似的miRNAs和EMT相关基因表达变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Expression changes of miRNAs and EMT-related genes in human mesothelial cells induced by long-term exposure to asbestos].

Objective: To investigate the effects of long-term exposure to chrysotile and crocidolite on miRNAs and epithelial mesenchymal transformation (EMT) -related gene expression in human pleural mesothelial cells. Methods: In November 2020, fluorescence quantitative polymerase chain reaction (RT-qPCR) was used to detect the expressions of EMT-related genes in human pleural mesothelioma cells (NCl-H2052 cells, NCl-H2452 cells) and human normal mesothelial cells (Met-5A cells). MiRNAs with abnormal expression in human pleural mesothelioma cells were screened out from the previous miRNA chip data of research group, and target genes of differentially expressed miRNAs were predicted using miRWalk database (http: //mirwalk.umm.uni-heidelberg.de). RT-qPCR was used to verify the abnormal expression of EMT-related miRNAs in cell lines. Met-5A cells were treated with 5μg/cm(2) chrysotile and crocidolite respectively for 48 h a time, once a week and a total of 10 times. Chrysotile group, crocidolite group and control group were set up. And the control group was added with the same volume of PBS. The expression changes of EMT-related genes and abnormal expression miRNAs in each group were detected by RT-qPCR. The differences among the groups were compared by one-way ANOVA, and the differences between the control group and the experimental group were compared by dunnet-t test. Results: Compared with Met-5A cells, the expression levels of Vimentin and Twist genes were increased, and the expression level of E-cadherin genes was decreased in NCl-H2052 cells and NCl-H2452 cells (P<0.001). Target genes of miRNAs with abnormal expression in miRNA chip were predicted, and the results showed four abnormally expressed miRNAs associated with EMT and verified the expression of these four miRNAs in the cell lines. Compared with Met-5A cells, the expression level of hsa-miR-155-5p was increased in NCl-H2052 cells and NCl-H2452 cells, the expression levels of hsa-miR-34b-5p, hsa-miR-34c-5p and hsa-miR-28-5p were decreased in NCl-H2052 cells and NCl-H2452 cells (P<0.001), which was consistent with the results of chip analysis. After exposure of Met-5A cells, it was found that compared with the control group, the expression levels of Vimentin and Twist genes, hsa-miR-155-5p, hsa-miR-34b-5p and hsa-miR-34c-5p in the crocidolite group were increased, while the expression level of E-cadherin gene was decreased (P<0.05). Compared with the control group, the expression levels of Vimentin, Twist and E-cadherin genes in chrysotile group were increased, while the expression levels of hsa-miR-34b-5p, hsa-miR-34c-5p and hsa-miR-28-5p were decreased (P<0.05) . Conclusion: Long-term exposure to chrysotile and crocidolite could cause Met-5A cells to produce miRNAs and EMT-related gene expression changes similar to mesothelioma cells.

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来源期刊
中华劳动卫生职业病杂志
中华劳动卫生职业病杂志 Medicine-Medicine (all)
CiteScore
1.00
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9764
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