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反映聚六亚甲基胍磷酸盐诱导A549人肺泡腺癌细胞纤维化的微小RNA调控网络。

MicroRNA regulatory networks reflective of polyhexamethylene guanidine phosphate-induced fibrosis in A549 human alveolar adenocarcinoma cells.

作者信息

Shin Da Young, Jeong Mi Ho, Bang In Jae, Kim Ha Ryong, Chung Kyu Hyuck

机构信息

School of Pharmacy, Sungkyunkwan University, Suwon, Gyeonggi-do, 16419, Republic of Korea.

College of Pharmacy, Catholic University of Daegu, Gyeongsan, Gyeongsangbuk-do, 38430, Republic of Korea.

出版信息

Toxicol Lett. 2018 May 1;287:49-58. doi: 10.1016/j.toxlet.2018.01.010. Epub 2018 Jan 12.

Abstract

Polyhexamethylene guanidine phosphate (PHMG-phosphate), an active component of humidifier disinfectant, is suspected to be a major cause of pulmonary fibrosis. Fibrosis, induced by recurrent epithelial damage, is significantly affected by epigenetic regulation, including microRNAs (miRNAs). The aim of this study was to investigate the fibrogenic mechanisms of PHMG-phosphate through the profiling of miRNAs and their target genes. A549 cells were treated with 0.75 μg/mL PHMG-phosphate for 24 and 48 h and miRNA microarray expression analysis was conducted. The putative mRNA targets of the miRNAs were identified and subjected to Gene Ontology analysis. After exposure to PHMG-phosphate for 24 and 48 h, 46 and 33 miRNAs, respectively, showed a significant change in expression over 1.5-fold compared with the control. The integrated analysis of miRNA and mRNA microarray results revealed the putative targets that were prominently enriched were associated with the epithelial-mesenchymal transition (EMT), cell cycle changes, and apoptosis. The dose-dependent induction of EMT by PHMG-phosphate exposure was confirmed by western blot. We identified 13 putative EMT-related targets that may play a role in PHMG-phosphate-induced fibrosis according to the Comparative Toxicogenomic Database. Our findings contribute to the comprehension of the fibrogenic mechanism of PHMG-phosphate and will aid further study on PHMG-phosphate-induced toxicity.

摘要

聚六亚甲基胍磷酸盐(PHMG-磷酸盐)是加湿器消毒剂的一种活性成分,被怀疑是肺纤维化的主要原因。由反复上皮损伤诱导的纤维化受到表观遗传调控的显著影响,包括微小RNA(miRNA)。本研究的目的是通过分析miRNA及其靶基因来探究PHMG-磷酸盐的致纤维化机制。用0.75μg/mL的PHMG-磷酸盐处理A549细胞24小时和48小时,并进行miRNA微阵列表达分析。鉴定出miRNA的假定mRNA靶标并进行基因本体分析。在暴露于PHMG-磷酸盐24小时和48小时后,分别有46个和33个miRNA的表达与对照相比有超过1.5倍的显著变化。miRNA和mRNA微阵列结果的综合分析显示,显著富集的假定靶标与上皮-间质转化(EMT)、细胞周期变化和细胞凋亡有关。通过蛋白质印迹证实了PHMG-磷酸盐暴露对EMT的剂量依赖性诱导。根据比较毒理基因组学数据库,我们鉴定出13个可能在PHMG-磷酸盐诱导的纤维化中起作用的假定EMT相关靶标。我们的研究结果有助于理解PHMG-磷酸盐的致纤维化机制,并将有助于进一步研究PHMG-磷酸盐诱导的毒性。

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