MicroRNA expression profiling defines the impact of electronic cigarettes on human airway epithelial cells.

Sci Rep

Division of Neonatology and Program in Pediatric Molecular and Personalized Medicine, Department of Pediatrics, University of Rochester Medical Center, Rochester, NY, USA.

Published: April 2017

AI Article Synopsis

  • eCig exposure significantly affects the expression of micro RNAs (miRNAs) in human lung epithelial cells, with 578 miRNAs being dysregulated following exposure.
  • The presence of nicotine and vaporization processes notably amplifies these effects, particularly leading to changes in 8 specific miRNAs.
  • Additionally, eCig exposure triggers oxidative stress-response genes and reduces the expression of key target genes like MYC and MRGPRX3, indicating potential health risks linked to eCig use.

Article Abstract

While all forms of tobacco exposure have negative health effects, the significance of exposure to electronic cigarettes (eCig) is not fully understood. Here, we studied the global effects of eCig on the micro RNA (miRNA) transcriptome in human lung epithelial cells. Primary human bronchial epithelial (NHBE) cells differentiated at air-liquid interface were exposed to eCig liquid. Exposure of NHBE to any eCig liquid resulted in the induction of oxidative stress-response genes including GCLM, GCLC, GPX2, NQO1 and HO-1. Vaporization of, and/or the presence of nicotine in, eCig liquid was associated with a greater response. We identified 578 miRNAs dysregulated by eCig exposure in NHBE, and 125 miRNA affected by vaporization of eCig liquid. Nicotine containing eCig vapor displayed the most profound effects upon miRNA expression. We selected 8 miRNAs (29A, 140, 126, 374A, 26A-2, 147B, 941 and 589) for further study. We validated increased expression of multiple miRNAs, including miR126, following eCig exposure. We also found significant reduction in the expression of two miR126 target genes, MYC and MRGPRX3, following exposure. These data demonstrated that eCig exposure has profound effects upon gene expression in human lung epithelial cells, some of which are epigenetically programmed at the level of miRNA regulation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430826PMC
http://dx.doi.org/10.1038/s41598-017-01167-8DOI Listing

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