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. 2019 Nov 7;9:16259. doi: 10.1038/s41598-019-52770-w

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Knock-down of miR-146a in non-CF and CF macrophages. (a,b) MiR-146a expression level in LPS-stimulated non-CF and CF macrophages. (c) MiR-155 expression in LPS-stimulated non-CF macrophages. MiRNAs were quantified 16 h after transfection with either the miR-146a inhibitor (α-miR-146a-5p) or the control inhibitor (Ctr) (n = 3). The data were normalised to expression of the endogenous RNU6B control. Data are means ± SEM. *p < 0.05; ***p < 0.001 (unpaired t-tests).