MicroRNA-101 attenuates pulmonary fibrosis by inhibiting fibroblast proliferation and activation

Chaoqun Huang, Xiao Xiao, Ye Yang, Amorite Mishra, Yurong Liang, Xiangming Zeng, Xiaoyun Yang, Dao Xu, Michael R. Blackburn, Craig A. Henke, Lin Liu

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74 Scopus citations


Aberrant proliferation and activation of lung fibroblasts contribute to the initiation and progression of idiopathic pulmonary fibrosis (IPF). However, the mechanisms responsible for the proliferation and activation of fibroblasts are not fully understood. The objective of this study was to investigate the role of miR-101 in the proliferation and activation of lung fibroblasts. miR-101 expression was determined in lung tissues from patients with IPF and mice with bleomycin-induced pulmonary fibrosis. The regulation of miR-101 and cellular signaling was investigated in pulmonary fibroblasts in vitro. The role of miR-101 in pulmonary fibrosis in vivo was studied using adenovirus-mediated gene transfer in mice. The expression of miR-101 was down-regulated in fibrotic lungs from patients with IPF and bleomycin-treated mice. The down-regulation of miR-101 occurred via the E26 transformation-specific (ETS) transcription factor. miR-101 suppressed the WNT5a-induced proliferation of lung fibroblasts by inhibiting NFATc2 signaling via targeting Frizzled receptor 4/6 and the TGF--induced activation of lung fibroblasts by inhibition of SMAD2/3 signaling via targeting the TGF- receptor 1. Adenovirus-mediated miR-101 gene transfer in the mouse lung attenuated bleomycin-induced lung fibrosis and improved lung function. Our data suggest that miR-101 is an anti-fibrotic microRNA and a potential therapeutic target for pulmonary fibrosis.

Original languageEnglish (US)
Pages (from-to)16420-16439
Number of pages20
JournalJournal of Biological Chemistry
Issue number40
StatePublished - Oct 6 2017

Bibliographical note

Funding Information:
Acknowledgments—This study utilized biological specimens and data provided by the Lung Tissue Research Consortium supported by the National Heart, Lung, and Blood Institute, National Institutes of Health.

Funding Information:
This work was supported by National Institutes of Health Grants R01HL116876, R03HL95383, and P20GM103648 (to L. L.) and R01HL125227 and P01HL 091775 (to C. A. H.). The authors declare that they have no conflicts of interest with the contents of this article. The con-tent is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Publisher Copyright:
© 2017 by The American Society for Biochemistry and Molecular Biology, Inc. Published in the U.S.A.


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