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. 2023 May 13;6:516. doi: 10.1038/s42003-023-04905-z

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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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Fig. 6 — a HRMVECs were transfected with control siRNA (siControl) or JunB siRNA (siJunB), after 48 h cell extracts were prepared and analysed for JunB levels by Western blotting and normalized to β-tubulin. b–e All the condition are same as in panel (a), except that the cells were analyzed for IL-33 (20 ng/mL)-induced migration (b), wound healing (c), tube formation (d), and sprouting assay (e). n = 6 (b, c, d, e) biologically independent samples per group, expressed as Mean ± SD. *P < 0.05 vs siControl, **p < 0.05 vs siControl + IL-33. Scale bar represents 50 μm in panel (e).