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MicroRNA Expression Analysis of Human Pulmonary Fibroblasts Treated with Acrolein

  • Hye Rim Park
  • , Seung Eun Lee
  • , Hyemi Kim
  • , Jongsung Lee
  • , Yong Seek Park

Research output: Contribution to journalArticlepeer-review

Abstract

Pulmonary fibroblasts are important structural lung cells that modulate tissue injury and immune response. It plays an important role in the inflammatory response by interacting between pulmonary fibroblasts and leukocytes. Cigarette smoke is known to trigger the development of diverse pulmonary and lung diseases, such as chronic obstructive pulmonary disease (COPD). α,β-unsaturated aldehydes such as acrolein (ACR) are present in cigarette smoke and are environment pollutants. ACR induces dysfunction of pulmonary and lung cells by forming DNA adducts and releasing inflammatory cytokines. MicroRNAs (miRNAs) are small interfering RNAs that negatively regulate mRNA gene expression and control the cellular response to toxic compounds. mRNAs also post-transcriptionally modulate gene expression. In this study, we identified whether the effects of ACR on the expression pattern of miRNAs in human pulmonary fibroblasts (HPFs). We carried out a pair-wise correlation analysis and examined 22 and 31 miRNAs with changed expression levels after treatment of HPFs with 10 μM and 25 μM ACR, respectively. Furthermore, we identified a significant anti-correlation in 102 and 17 mRNAs. Differentially expressed miRNAs and signaling pathways were further analyzed by gene ontology enrichment analysis. Our results showed that altered expression of miRNAs by ACR treatment was relevant in the dysfunction of respiratory cells and might contribute to the understanding of the mechanism of pulmonary diseases.

Original languageEnglish
Pages (from-to)231-239
Number of pages9
JournalBiochip Journal
Volume12
Issue number3
DOIs
StatePublished - 1 Sep 2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acrolein
  • Chronic obstructive pulmonary disease
  • miRNA
  • Pulmonary fibroblasts

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