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Fig. 4 | Journal of Inflammation

Fig. 4

From: The role of N-glycosylation of CD200-CD200R1 interaction in classical microglial activation

Fig. 4

N44Q mutant enhanced neuronal death. N44Q mutant enhanced neuronal death: role of CD200-CD200R dysfunction. Resting or LPS stimulated BV2 cells transfected with WT or N44Q were cultured with neurons. Cortical neurons were co-cultured with BV2 cells for up to 24 h and neuronal death was estimated by LDH measurement in the media. The increased neuronal death induced by LPS stimulated BV2 cells was enhanced by the treatment with anti-CD200 antibody (*p < 0.01, WT + LPS vs WT; +p < 0.01, N44Q + LPS vs N44Q; ANOVA; n = 3). BV2 cells transfected with N44Q mutant leaded to the reinforced neuronal death (*p < 0.01; +p < 0.01; ANOVA; n = 3; #p < 0.05, WT + LPS + anti-CD200 vs WT + LPS; ##p > 0.05, N44Q + LPS + anti-CD200 vs N44Q + LPS; &p > 0.05, WT + LPS + anti-CD200 vs N44Q + LPS). Error bars indicate ± SEM. These data suggested N44Q mutant impaired CD200-CD200R1 interaction and subsequently leaded to microglial activation and neuronal death

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