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. Author manuscript; available in PMC: 2022 May 10.
Published in final edited form as: J Immunol. 2022 Mar 2;208(6):1509. doi: 10.4049/jimmunol.2101213

Figure 3. Activation of NF-κB, MAPK, and NADPH oxidase, and expression of adhesion molecule ICAM-1 were impaired in cxcl1−/− mice following PMS.

Figure 3

A, CXCL1 is essential for the activation of NF-κB during PMS induction. Phosphorylation of NF-κB/p65(ser 536), and IκBα in the homogenates from liver, lung and spleen kidney from cxcl1−/− as compared to WT mice. B, Attenuated activation of MAPKs in the organs of cxcl1−/− mice. Phosphorylated p38-MAPK, ERK, and JNK in the homogenates from different organs from cxcl1−/− and WT mice were probed with their respective antibodies. C, Expression of adhesion molecule ICAM-1 but not VCAM-1 is reduced in cxcl1−/− mice. The expression level of ICAM-1 and VCAM-1 were determined in the organs of cxcl1−/− and WT control mice following PMS for time points 6 and 24 h. D, The activation of NADPH oxidase is impaired in cxcl1−/− mice. The expression levels of Nox2, p22phox, p67phox, and p47phox were determined in the homogenates of organs of cxcl1−/− and WT control mice by immunoblotting at 6 and 24 h post-PMS. GAPDH or total p38 expression levels were assessed in all samples as internal loading control and the blots are representative of 2 independent experiments with similar results (A, B, C, and D). (n=4–6/group).

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