Department of Environmental Sciences and Engineering, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, USA.
Environ Health Perspect. 2013 Mar;121(3):339-44. doi: 10.1289/ehp.1205582. Epub 2013 Jan 15.
Formaldehyde is an air pollutant present in both indoor and outdoor atmospheres. Because of its ubiquitous nature, it is imperative to understand the mechanisms underlying formaldehyde-induced toxicity and carcinogenicity. MicroRNAs (miRNAs) can influence disease caused by environmental exposures, yet miRNAs are understudied in relation to formaldehyde. Our previous investigation demonstrated that formaldehyde exposure in human lung cells caused disruptions in miRNA expression profiles in vitro.
Using an in vivo model, we set out to test the hypothesis that formaldehyde inhalation exposure significantly alters miRNA expression profiles within the nasal epithelium of nonhuman primates.
Cynomolgus macaques were exposed by inhalation to approximately 0, 2, or 6 ppm formaldehyde for 6 hr/day for 2 consecutive days. Small RNAs were extracted from nasal samples and assessed for genome-wide miRNA expression levels. Transcriptional targets of formaldehyde-altered miRNAs were computationally predicted, analyzed at the systems level, and assessed using real-time reverse transcriptase polymerase chain reaction (RT-PCR).
Expression analysis revealed that 3 and 13 miRNAs were dysregulated in response to 2 and 6 ppm formaldehyde, respectively. Transcriptional targets of the miRNA with the greatest increase (miR-125b) and decrease (miR-142-3p) in expression were predicted and analyzed at the systems level. Enrichment was identified for miR-125b targeting genes involved in apoptosis signaling. The apoptosis-related targets were functionally tested using RT-PCR, where all targets showed decreased expression in formaldehyde-exposed samples.
Formaldehyde exposure significantly disrupts miRNA expression profiles within the nasal epithelium, and these alterations likely influence apoptosis signaling.
甲醛是一种存在于室内和室外大气中的空气污染物。由于其无处不在的性质,了解甲醛诱导的毒性和致癌性的机制势在必行。microRNAs(miRNAs)可以影响环境暴露引起的疾病,但关于甲醛与 miRNAs 的关系研究还很不足。我们之前的研究表明,甲醛暴露在人肺细胞中会导致体外 miRNA 表达谱的紊乱。
我们使用体内模型,检验假设,即甲醛吸入暴露会显著改变非人类灵长类动物鼻上皮内的 miRNA 表达谱。
恒河猴通过吸入暴露于约 0、2 或 6ppm 的甲醛中,每天 6 小时,连续 2 天。从小鼻样本中提取小 RNA,并评估全基因组 miRNA 表达水平。通过计算机预测甲醛改变的 miRNA 的转录靶标,在系统水平上进行分析,并使用实时逆转录聚合酶链反应(RT-PCR)进行评估。
表达分析显示,分别有 3 个和 13 个 miRNA 对 2ppm 和 6ppm 甲醛的反应出现失调。miRNA 表达增加(miR-125b)和减少(miR-142-3p)最大的转录靶标在系统水平上进行了预测和分析。鉴定到 miR-125b 靶向基因参与凋亡信号的富集。使用 RT-PCR 对凋亡相关靶标进行功能测试,结果显示所有靶标在甲醛暴露样本中的表达均下降。
甲醛暴露会显著扰乱鼻上皮内的 miRNA 表达谱,这些改变可能会影响凋亡信号。