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. 2021 Jan 15;12(1):86. doi: 10.1038/s41419-020-03305-z

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© The Author(s) 2021

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 — HaCaT cells were cotransfected with si-SPRR2C and antagomir-330-5p under L-22 stimulation and examined for (A) the protein levels of STAT1 and S100A7 by immunoblotting; B the cell viability by MTT assays; C DNA synthesis by EdU assays; D the protein levels of KRT5/14/1/10 by immunoblotting; E and the mRNA expression levels of IL-1β, IL-6, and TNF-α by real-time PCR. *P < 0.05, **P < 0.01, compared to the control group; ^#P < 0.05, ^##P < 0.01, compared to the si-NC+ antagomir-330-5p group.