Department of Environmental Medicine, School of Medicine and Dentistry, University of Rochester Medical Center, University of Rochester, Rochester, New York.
Department of Environmental Medicine, School of Medicine, New York University, New York, New York; and.
Am J Respir Cell Mol Biol. 2020 Dec;63(6):794-805. doi: 10.1165/rcmb.2020-0036OC.
Electronic-cigarette (e-cig) vaping is a serious concern, as many pregnant women who vape consider it safe. However, little is known about the harmful effects of prenatal e-cig exposure on adult offspring, especially on extracellular-matrix (ECM) deposition and myogenesis in the lungs of offspring. We evaluated the biochemical and molecular implications of maternal exposure during pregnancy to e-cig aerosols on the adult offspring of both sexes, with a particular focus on pulmonary ECM remodeling and myogenesis. Pregnant CD-1 mice were exposed to e-cig aerosols with or without nicotine, throughout gestation, and lungs were collected from adult male and female offspring. Compared with the air-exposed control group, female mice exposed to e-cig aerosols, with or without nicotine, demonstrated increased lung protein abundance of LEF-1 (lymphoid enhancer-binding factor 1), fibronectin, and E-cadherin, whereas altered E-cadherin and PPARγ (peroxisome proliferator-activated receptor γ) levels were observed only in males exposed to e-cig aerosols with nicotine. Moreover, lipogenic and myogenic mRNAs were dysregulated in adult offspring in a sex-dependent manner. PAI-1 (plasminogen activator inhibitor-1), one of the ECM regulators, was significantly increased in females exposed prenatally to e-cig aerosols with nicotine and in males exposed to e-cig aerosols compared with control animals exposed to air. MMP9 (matrix metalloproteinase 9), a downstream target of PAI-1, was downregulated in both sexes exposed to e-cig aerosols with nicotine. No differences in lung histology were observed among any of the treatment groups. Overall, adult mice exposed prenatally to e-cig aerosols could be predisposed to developing pulmonary disease later in life. Thus, these findings suggest that vaping during pregnancy is unsafe and increases the propensity for later-life interstitial lung diseases.
电子香烟(电子烟)蒸气是一个严重的问题,因为许多吸食电子烟的孕妇认为它是安全的。然而,对于产前电子烟暴露对成年后代的有害影响,特别是对后代肺部细胞外基质(ECM)沉积和肌发生的影响,知之甚少。我们评估了在怀孕期间暴露于电子烟气溶胶对雌雄后代的生化和分子影响,特别关注肺部 ECM 重塑和肌发生。怀孕的 CD-1 小鼠在整个妊娠期暴露于含或不含尼古丁的电子烟气溶胶中,并从成年雄性和雌性后代中收集肺部。与空气暴露的对照组相比,暴露于电子烟气溶胶(含或不含尼古丁)的雌性小鼠的肺蛋白 LEF-1(淋巴增强结合因子 1)、纤维连接蛋白和 E-钙粘蛋白的丰度增加,而仅在暴露于含尼古丁的电子烟气溶胶的雄性小鼠中观察到 E-钙粘蛋白和 PPARγ(过氧化物酶体增殖物激活受体 γ)水平的改变。此外,脂肪生成和肌生成 mRNA 以性别依赖的方式在成年后代中失调。ECM 调节剂之一的 PAI-1(纤溶酶原激活物抑制剂-1)在暴露于产前电子烟气溶胶(含尼古丁)的雌性和暴露于电子烟气溶胶的雄性中显著增加,与暴露于空气的对照动物相比。PAI-1 的下游靶标 MMP9(基质金属蛋白酶 9)在暴露于含尼古丁的电子烟气溶胶的雌雄中均下调。在任何治疗组之间都没有观察到肺组织学的差异。总体而言,产前暴露于电子烟气溶胶的成年小鼠可能易患晚年肺部疾病。因此,这些发现表明,怀孕期间吸食电子烟是不安全的,会增加晚年间质性肺病的倾向。