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. 2019 Jun 21;10:2730. doi: 10.1038/s41467-019-10646-7

Fig. 4.

Fig. 4

Lugdunin amplifies the commensal-induced chemokine (C-X-C motif) ligand (CXCL8) induction. a Primary human keratinocytes (PHKs) were either treated with 2 μM of human antimicrobial peptides (AMPs) (black bars) or lugdunin (blue bars), or 0.8 μM (pro)-gallidermin or nisin (black bars), or in combination with S. epidermidis conditioned medium (CM) (gray and red striped bars) for 5 h, and subsequently expression of CXCL8 was analyzed and normalized to actin. Shown is one representative experiment of three independent experiments with two technical replicates ± s.e.m. b PHKs were treated with 2 μM human AMPs, 2 μM lugdunin, 0.8 μM of the other bacteriocins (gray bars) or the correspondent peptide combinations (white bars), or 50 ng/mL Pam2Cys, 10 ng/mL IL-1α, or S. epidermidis CM as controls (black bars), for 5 h and subsequently expression of CXCL8 was analyzed and normalized to actin. Shown is one representative experiment of three independent experiments with two technical replicates ± s.e.m. Significant differences to control treatments were analyzed by ordinary one-way analysis of variance (ANOVA) followed by Dunnett’s multiple comparisons test (***P < 0.001; ****P < 0.0001). Source data are provided as a Source Data file