Publication: MIR-34 MIRNAs regulate cellular senescence in type II alveolar epithelial cells of patients with idiopathic pulmonary fibrosis
Issued Date
2016-06-01
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ISSN
19326203
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2-s2.0-84977270999
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Mahidol University
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SCOPUS
Bibliographic Citation
PLoS ONE. Vol.11, No.6 (2016)
Suggested Citation
Supparerk Disayabutr, Eun Kyung Kim, Seung Ick Cha, Gary Green, Ram P. Naikawadi, Kirk D. Jones, Jeffrey A. Golden, Aaron Schroeder, Michael A. Matthay, Jasleen Kukreja, David J. Erle, Harold R. Collard, Paul J. Wolters MIR-34 MIRNAs regulate cellular senescence in type II alveolar epithelial cells of patients with idiopathic pulmonary fibrosis. PLoS ONE. Vol.11, No.6 (2016). doi:10.1371/journal.pone.0158367 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/41470
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Title
MIR-34 MIRNAs regulate cellular senescence in type II alveolar epithelial cells of patients with idiopathic pulmonary fibrosis
Abstract
Pathologic features of idiopathic pulmonary fibrosis (IPF) include genetic predisposition, activation of the unfolded protein response, telomere attrition, and cellular senescence. The mechanisms leading to alveolar epithelial cell (AEC) senescence are poorly understood. MicroRNAs (miRNAs) have been reported as regulators of cellular senescence. Senescence markers including p16, p21, p53, and senescence-associated β-galactosidase (SA-βgal) activity were measured in type II AECs from IPF lungs and unused donor lungs. miRNAs were quantified in type II AECs using gene expression arrays and quantitative RT-PCR. Molecular markers of senescence (p16, p21, and p53) were elevated in IPF type II AECs. SA-βgal activity was detected in a greater percentage in type II AECs isolated from IPF patients (23.1%) compared to patients with other interstitial lung diseases (1.2%) or normal controls (0.8%). The relative levels of senescence-associated miRNAs miR-34a, miR-34b, and miR-34c, but not miR-20a, miR-29c, or miR-let-7f were significantly higher in type II AECs from IPF patients. Overexpression of miR-34a, miR-34b, or miR-34c in lung epithelial cells was associated with higher SA-βgal activity (27.8%, 35.1%, and 38.2%, respectively) relative to control treated cells (8.8%). Targets of miR-34 miRNAs, including E2F1, c-Myc, and cyclin E2, were lower in IPF type II AECs. These results show that markers of senescence are uniquely elevated in IPF type II AECs and suggest that the miR-34 family of miRNAs regulate senescence in IPF type II AECs.