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. 2021 Feb 8;4:172. doi: 10.1038/s42003-021-01703-3

Fig. 3. IL-36γ is an upstream amplifier in mouse macrophages and fibroblasts.

Fig. 3

a Relative mRNA amounts of Il36r in naive mouse bone marrow-derived macrophages (BMDMs, n = 6) in response to no stimulation (−) or stimulation with GM-CSF and IL-36γ. b CXCL1 protein concentrations in supernatant of BMDMs (n = 4) after no stimulation (−), or stimulation with IL-36αβγ. IL-1α, IL-1β alone, or in combination with GM-CSF and TGFβ c, d Relative mRNA amounts of Il36g, Cxcl1, Il1a, Il1b, Il1r1, Il1rn, and Il36rn in BMDMs (n = 4) (c) and primary mouse fibroblasts (n = 4) (d) after no stimulation (−) or stimulation with IL-36αβγ, IL-1α, IL-1β alone, or in combination with GM-CSF and TGF-β. e Relative mRNA amounts in primary mouse fibroblasts (n = 4) of Il36r after no stimulation (−) or stimulation with IL-36αβγ or GM-CSF and TGF-β. Shown are the mean values ± SEM of biological replicates. ad *P ≤ 0.05, **P ≤ 0.01, ***P ≤ 0.001, ****P ≤ 0.0001 vs all other groups by one-way ANOVA and Tukey’s correction. e *P ≤ 0.05, vs untreated by t test.