4.3 Article

Fetal e-cigarette exposure programs a neonatal brain hypoxic-ischemic sensitive phenotype via altering DNA methylation patterns and autophagy signaling pathway

出版社

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00207.2021

关键词

autophagy; DNA methylation; e-cigarette; HIE; ROS

资金

  1. National Institutes of Health [HL135623, DA041492, HD088039]
  2. Regents of the University of California, Research Grants Program Office, Tobacco-Related Disease Research Program (TRDRP) [T29IR0437, T30FT0936]

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The study demonstrates that maternal e-cigarette exposure can reduce body weight and brain weight in neonates, but increase the brain-to-body weight ratio. Additionally, e-cigarette exposure can increase the sensitivity of male neonates to hypoxic-ischemic brain injury and regulate autophagy-related gene expression through DNA methylation.
Maternal e-cigarette (e-cig) exposure is a pressing perinatal health concern. Emerging evidence reveals its potential adverse impacts on brain development in offspring, yet the underlying mechanisms are poorly understood. The present study tested the hypothesis that fetal e-cig exposure induces an aberrant DNA methylation profile in the developing brain, leading to alteration of autophagic flux signaling and programming of a sensitive phenotype to neonatal hypoxic-ischemic encephalopathy (HIE). Pregnant rats were exposed to chronic intermittent e-cig aerosol. Neonates were examined at the age of 9 days old. Maternal e-cig exposure decreased the body weight and brain weight but enhanced the brain-to-body weight ratio in the neonates. E-cig exposure induced a gender-dependent increase in hypoxic-ischemia-induced brain injury in male neonates associated with enhanced reactive oxygen species (ROS) activity. It differentially altered DNA methyltransferase expression and enhanced both global DNA methylation levels and specific CpG methylation at the autophagy-related gene 5 (ATG5) promoter. In addition, maternal e-cig exposure caused downregulations of ATG5, microtubule-associated protein 1 light chain 3b, and sirtuin 1 expression in neonatal brains. Of importance, knockdown of ATG5 in neonatal pups exaggerated neonatal HIE. In conclusion, the present study reveals that maternal e-cig exposure downregulates autophagy-related gene expression via DNA hypermethylation, leading to programming of a hypoxic-ischemic sensitive phenotype in the neonatal brain.

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