College of Environment and Resource, Research Center of Environment and Health, Shanxi University, Taiyuan, Shanxi 030006, PR China.
Department of Environmental Health, School of Public Health, Shanxi Medical University, Taiyuan, Shanxi 030001, PR China.
Ecotoxicol Environ Saf. 2022 Nov;246:114140. doi: 10.1016/j.ecoenv.2022.114140. Epub 2022 Oct 6.
Gestation is a sensitive window to nitrogen dioxide (NO) exposure, which may disturb fetal lung development and lung function later in life. Animal and epidemiological studies indicated that long noncoding RNAs (lncRNAs) participate in abnormal lung development induced by environmental pollutant exposure. In the present study, pregnant C57BL/6J mice were exposed to 2.5 ppm NO (mimicking indoor occupational exposure) or clean air, and lncRNAs expression profiles in the lungs of offspring mice were determined by lncRNA-seq on embryonic day 13.5 (E13.5), E18.5, postnatal day 1 (P1), and P14. The lung histopathology examination of offspring was performed, followed by weighted gene coexpression network analysis (WGCNA), prediction of lncRNAs-target genes, and the biological processes enrichment analysis of lncRNAs. Our results indicated that maternal NO exposure induced hypoalveolarization on P14 and differentially expressed lncRNAs showed a time-series pattern. Following WGCNA and enrichment analysis, 2 modules participated in development-related pathways. Importantly, the expressions of related genes were altered, some of which were confirmed to be related to abnormal vascular development and even lung diseases. The research points out that the maternal NO exposure leads to abnormal lung development in offspring that might be related to altered lncRNAs expression profiles with time-series-pattern.
妊娠是对二氧化氮(NO)暴露敏感的时期,可能会干扰胎儿肺部发育,并在以后的生活中影响肺功能。动物和流行病学研究表明,长链非编码 RNA(lncRNA)参与了环境污染物暴露引起的异常肺部发育。在本研究中,用 2.5 ppm 的 NO(模拟室内职业暴露)或清洁空气对怀孕的 C57BL/6J 小鼠进行暴露,然后通过 lncRNA-seq 在胚胎第 13.5 天(E13.5)、E18.5、出生后第 1 天(P1)和 P14 检测后代小鼠肺部的 lncRNA 表达谱。对后代的肺部组织病理学检查后,进行加权基因共表达网络分析(WGCNA)、lncRNA-靶基因预测以及 lncRNA 的生物学过程富集分析。我们的研究结果表明,母体 NO 暴露在 P14 时引起肺泡发育不全,差异表达的 lncRNA 呈现时间序列模式。经过 WGCNA 和富集分析,有 2 个模块参与了发育相关的通路。重要的是,相关基因的表达发生了改变,其中一些基因与异常血管发育甚至肺部疾病有关。该研究指出,母体 NO 暴露会导致后代肺部发育异常,这可能与时间序列模式下改变的 lncRNA 表达谱有关。