Fig. 4: LAPTM5 is upregulated and associated with the activation of the STING signaling pathway in macrophages in rosacea. | Communications Biology

Fig. 4: LAPTM5 is upregulated and associated with the activation of the STING signaling pathway in macrophages in rosacea.

From: LAPTM5 exacerbates STING-mediated inflammation induced by LL-37 through stabilizing STING in rosacea

Fig. 4

AC Analysis of the expression levels of LAPTM5 in skin samples from rosacea patients (GSE65914 and HRA000378) and LL-37-induced rosacea-like mice (GSE147950). D, E Scatter plots showing positive correlation of LAPTM5 expression in rosacea skin (GSE65914) and macrophage marker CD68 (D) and STING (E). F, G IHC of LAPTM5 in skin tissues from healthy controls (HC) and rosacea patients (F). Quantification of staining intensity (IOD/Area) for LAPTM5 in the IHC images of rosacea patients and HC (G). n = 5 for each group. HJ IHC of LAPTM5 in skin tissues from control and LL-37-induced rosacea-like mice (H). Quantification of staining intensity (IOD/Area) for LAPTM5 in the IHC images of LL-37-induced rosacea-like mice and control (I). n = 6 for each group. J Immunoblotting analysis of LAPTM5 protein expression in skin tissue lysates from control and LL-37-induced rosacea-like mice. K Immunofluorescence staining of F4/80 (red) and LAPTM5 (green) in skin sections from LL-37- or H-151-treated mice. Nuclei are stained with DAPI (blue). The merged and zoom-in images highlight co-localization of F4/80 and LAPTM5. Scale bars: 100 µm. LN Quantification of relative fluorescence intensity for LAPTM5 (L) and F4/80 (M) in skin sections from LL-37- or H-151-treated mice. LAPTM5 and F4/80 colocalization (N), expressed as the percentage of double-positive cells relative to total F4/80-positive cells in three randomly selected fields for each sample. Scale bar: 100 µm, n = 6 for each group. O Immunoblot analysis of STING and LAPTM5 expression in skin tissue lysates from mice treated with LL-37, H-151, or LL-37 plus H-151. P, Q Immunoblot analysis of pSTING, STING, pIRF3, IRF3, pNF-κB p65, NF-κB p65, and LAPTM5 in cell lysates from RAW264.7 and L929 cells exposed to increasing concentrations of LL-37 (0, 1, 2, 4, and 8 µM) for 24 h. Data represent the mean ± SEM, **p < 0.01, ***p < 0.001, ****p < 0.0001. Two-tailed unpaired Student’s t-test or One-way ANOVA with Bonferroni’s post hoc test was used. All results are representative of at least three independent experiments.

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