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Fig. 3 | Journal of Neuroinflammation

Fig. 3

From: NOX2 deficiency alters macrophage phenotype through an IL-10/STAT3 dependent mechanism: implications for traumatic brain injury

Fig. 3

STAT1 activation is attenuated in NOX2−/− BMDMs, whereas STAT6 activation is unchanged. (a, b) Protein expression of phosphorylated STAT1 and phosphorylated STAT6 in response to LPS/IL-4 stimulation was assessed by western immunoblotting. (c) LPS/IL-4 (both 10 ng/ml; 24 h) increased pSTAT1 expression (** P * < 0.001, ANOVA) in WT BMDMs. In contrast, LPS/IL-4-induced increase in pSTAT1 was significantly reduced in NOX2−/− BMDMs (+ P < 0.05, WT LPS/IL-4 vs. NOX2−/− LPS/IL-4; ANOVA). (d) LPS/IL-4 significantly increased pSTAT6 (*** P < 0.001; ANOVA) in WT and NOX2−/− BMDMs, but no genotype related differences were observed. All data are expressed as means (± SEM n = 5)

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