Upregulated microRNA-125b-5p in patients with asthma-COPD overlap mediates oxidative stress and late apoptosis via targeting IL6R/TRIAP1 signaling

Respir Res. 2024 Feb 1;25(1):64. doi: 10.1186/s12931-024-02703-7.

Abstract

Background: Among patients with chronic obstructive pulmonary disease (COPD), some have features of both asthma and COPD-a condition categorized as asthma-COPD overlap (ACO). Our aim was to determine whether asthma- or COPD-related microRNAs (miRNAs) play a role in the pathogenesis of ACO.

Methods: A total of 22 healthy subjects and 27 patients with ACO were enrolled. We selected 6 miRNAs that were found to correlate with COPD and asthma. The expression of miRNAs and target genes was analyzed using quantitative reverse-transcriptase polymerase chain reaction. Cell apoptosis and intracellular reactive oxygen species production were evaluated using flow cytometry. In vitro human monocytic THP-1 cells and primary normal human bronchial epithelial (NHBE) cells under stimuli with cigarette smoke extract (CSE) or ovalbumin (OVA) allergen or both were used to verify the clinical findings.

Results: We identified the upregulation of miR-125b-5p in patients with ACO and in THP-1 cells stimulated with CSE plus OVA allergen. We selected 16 genes related to the miR-125b-5p pathway and found that IL6R and TRIAP1 were both downregulated in patients with ACO and in THP-1 cells stimulated with CSE plus OVA. The percentage of late apoptotic cells increased in the THP-1 cell culture model when stimulated with CSE plus OVA, and the effect was reversed by transfection with miR-125b-5p small interfering RNA (siRNA). The percentage of reactive oxygen species-producing cells increased in the NHBE cell culture model when stimulated with CSE plus OVA, and the effect was reversed by transfection with miR-125b-5p siRNA. In NHBE cells, siRNA transfection reversed the upregulation of STAT3 under CSE+OVA stimulation.

Conclusions: Our study revealed that upregulation of miR-125b-5p in patients with ACO mediated late apoptosis in THP-1 cells and oxidative stress in NHBE cells via targeting IL6R and TRIAP1. STAT3 expression was also regulated by miR-125b-5p.

Keywords: Asthma-COPD overlap; Interleukin 6 receptor; TP53-regulated inhibitor of apoptosis 1; miR-125b-5p.

MeSH terms

  • Aged
  • Allergens
  • Apoptosis* / genetics
  • Asthma* / complications
  • Asthma* / genetics
  • Humans
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Male
  • MicroRNAs* / metabolism
  • Oxidative Stress / genetics
  • Pulmonary Disease, Chronic Obstructive* / metabolism
  • RNA, Small Interfering / metabolism
  • Reactive Oxygen Species
  • Receptors, Interleukin-6 / metabolism

Substances

  • Allergens
  • IL6R protein, human
  • Intracellular Signaling Peptides and Proteins
  • MicroRNAs
  • MIRN125 microRNA, human
  • Reactive Oxygen Species
  • Receptors, Interleukin-6
  • RNA, Small Interfering
  • TRIAP1 protein, human