Role of miR-146a in the regulation of inflammation in an in vitro model of graves’ orbitopathy

Sun Young Jang, Min Kyung Chae, Joon H. Lee, Eun Jig Lee, Jin Sook Yoon

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37 Citations (Scopus)


PURPOSE. To investigate the role of microRNA 146a (miR-146a) in the regulation of inflammation in an in vitro model of Graves’ orbitopathy (GO). METHODS. The level of miR-146a expression in orbital adipose tissue was compared between GO and non-GO by quantitative real-time PCR (qPCR). The effects of interleukin 1β (IL-1β) on miR-146a expression were analyzed in orbital fibroblasts by qPCR. To investigate the molecular mechanism underlying IL-1β -induced miR-146a expression, the effects of inhibitors of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB), mitogenactivated protein kinase/extracellular signal-regulated kinases (MEK)-1/2, c-Jun N-terminal kinases (JNK)-1/2, p38 MAP kinase, and phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K) were analyzed. The effects of miR-146a mimics and inhibitors on IL-1β -induced IL-6 release were examined by ELISA and Western blotting. RESULTS. The level of miR-146a expression was significantly higher in GO orbital adipose tissue than in non-GO (P = 0.032). Interleukin 1b induced a time- and concentration-dependent increase in miR-146a expression. Interleukin 1β (10 ng/mL, 16 hours) induced an approximately 17.5-fold increase in miR-146 expression. The increase in miR-146a expression by IL-1β was significantly inhibited by NF-κB, JNK-1/2, and PI3K inhibitors (1.94 ± 0.25, 5.28 ± 0.34 and 9.73 ± 2.32-fold, respectively, P < 0.05 compared with IL-1β -induced miR- 146 expression, independent t-test). Interleukin 1β -induced IL-6 protein production was further decreased by miR-146a mimics, but not by inhibitors of miR-146a. CONCLUSIONS. MicroRNA 146a was upregulated by inflammatory stress in orbital fibroblasts. Our results indicated that miR-146a had a positive effect on the anti-inflammatory process. MicroRNA 146a may play a role in the regulation of inflammation in orbital fibroblasts, and may participate in the pathogenesis of GO.

Original languageEnglish
Article number05
Pages (from-to)4027-4034
Number of pages8
JournalInvestigative Ophthalmology and Visual Science
Issue number10
Publication statusPublished - 2016 Aug 1

Bibliographical note

Publisher Copyright:
© 2015, Association for Research in Vision and Ophthalmology Inc. All rights reserved.

All Science Journal Classification (ASJC) codes

  • Ophthalmology
  • Sensory Systems
  • Cellular and Molecular Neuroscience


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