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Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA
MicroRNAs (miRNAs), a family of small non-coding RNAs, serve a pivotal role in the regulation of the inflammation by modulating the expression of various genes. However, the molecular mechanism by which miRNAs regulate inflammation-associated molecules in oral epithelial cells remains to be elucidat...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223109/ https://www.ncbi.nlm.nih.gov/pubmed/34132371 http://dx.doi.org/10.3892/mmr.2021.12220 |
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author | Kawasaki, Hiromichi Amano, Hirotaka |
author_facet | Kawasaki, Hiromichi Amano, Hirotaka |
author_sort | Kawasaki, Hiromichi |
collection | PubMed |
description | MicroRNAs (miRNAs), a family of small non-coding RNAs, serve a pivotal role in the regulation of the inflammation by modulating the expression of various genes. However, the molecular mechanism by which miRNAs regulate inflammation-associated molecules in oral epithelial cells remains to be elucidated. The present study examined the biological function of miR-429 by performing the gain-/loss-of-function studies of miR-429 in a gingival squamous cell carcinoma line Ca9-22 cells that either over- or under-expressed miR-429 through transient transfection with miR-429 mimic or miR-429 inhibitor, respectively. The results demonstrated that the over-expression of miR-429 suppressed the mRNA level of several interleukins, including IL-8. In addition, the over-expression of miR-429 reduced IL-8 secretion under the basal and TNF-α stimulated conditions, whereas the secretion of IL-8 was enhanced when miR-429 was under-expressed. The over-expression of miR-429 inhibited the activation of the transcription factor NF-κB. Furthermore, we found that miR-429 suppressed both mRNA and protein levels of IKKβ via its direct binding to the 3′-untranslated region of IKKβ mRNA. In addition, the downregulation of IKKβ by small interfering RNA reduced both NF-kB activity and IL-8 production in Ca9-22 cells. Taken together, the findings revealed the molecular mechanism of miR-429 to regulate the inflammatory mediator in gingival cells and suggested that it could be useful as a therapeutic target of oral inflammatory diseases. |
format | Online Article Text |
id | pubmed-8223109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-82231092021-06-26 Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA Kawasaki, Hiromichi Amano, Hirotaka Mol Med Rep Articles MicroRNAs (miRNAs), a family of small non-coding RNAs, serve a pivotal role in the regulation of the inflammation by modulating the expression of various genes. However, the molecular mechanism by which miRNAs regulate inflammation-associated molecules in oral epithelial cells remains to be elucidated. The present study examined the biological function of miR-429 by performing the gain-/loss-of-function studies of miR-429 in a gingival squamous cell carcinoma line Ca9-22 cells that either over- or under-expressed miR-429 through transient transfection with miR-429 mimic or miR-429 inhibitor, respectively. The results demonstrated that the over-expression of miR-429 suppressed the mRNA level of several interleukins, including IL-8. In addition, the over-expression of miR-429 reduced IL-8 secretion under the basal and TNF-α stimulated conditions, whereas the secretion of IL-8 was enhanced when miR-429 was under-expressed. The over-expression of miR-429 inhibited the activation of the transcription factor NF-κB. Furthermore, we found that miR-429 suppressed both mRNA and protein levels of IKKβ via its direct binding to the 3′-untranslated region of IKKβ mRNA. In addition, the downregulation of IKKβ by small interfering RNA reduced both NF-kB activity and IL-8 production in Ca9-22 cells. Taken together, the findings revealed the molecular mechanism of miR-429 to regulate the inflammatory mediator in gingival cells and suggested that it could be useful as a therapeutic target of oral inflammatory diseases. D.A. Spandidos 2021-08 2021-06-14 /pmc/articles/PMC8223109/ /pubmed/34132371 http://dx.doi.org/10.3892/mmr.2021.12220 Text en Copyright: © Kawasaki et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Kawasaki, Hiromichi Amano, Hirotaka Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA |
title | Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA |
title_full | Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA |
title_fullStr | Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA |
title_full_unstemmed | Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA |
title_short | Anti-inflammatory role of microRNA-429 in human gingival epithelial cells-inhibition of IL-8 production through direct binding to IKKβ mRNA |
title_sort | anti-inflammatory role of microrna-429 in human gingival epithelial cells-inhibition of il-8 production through direct binding to ikkβ mrna |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223109/ https://www.ncbi.nlm.nih.gov/pubmed/34132371 http://dx.doi.org/10.3892/mmr.2021.12220 |
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