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. 2021 Apr 9;22:25. doi: 10.1186/s12865-021-00417-9

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© The Author(s) 2021

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 6 — Influence of ERK, NFκB p65, and NFAT inhibitors on IFN-γ production by NK and CD4⁺ T cells. a–b Representative flow cytometry plots and statistical analyses of IFN-γ production following treatment with PD98059 (ERK inhibitor), PDTC (NFκB p65 inhibitor), 480401-M (NFAT inhibitor), PD98059 + PDTC, or PD98059 + PDTC + 480401-M, in NK cells (n = 4). c–d Representative flow cytometry plots and statistical analyses of IFN-γ production following PD98059, PDTC, 480401-M, PD98059 + PDTC, or PD98059 + PDTC + 480401-M treatment in CD4⁺ T cells (n = 4). All data analyzed using FacsDiva™ 8.0.3 (URL: www.bdbiosciences.com) and FlowJo™ 10.5.0 (URL: www.flowjo.com/flowjo-eula/). Wilcoxon matched-pairs signed rank tests (GraphPad Prism 9.0, URL: www.graphpad.com) were used to compare the two groups; ^*p < 0.05, ^**p < 0.01, ^***p < 0.001, ^****p < 0.0001