GSDMD depletion in neutrophils attenuates the development of skin inflammation in psoriasis.
a) Representative images of western blot showing the expression of GSDMD in bone marrow-derived neutrophils of cKO and isotype control mice.
b) Macroscopic phenotypic representation of the dorsal skin in control and GSDMD-cKO mice treated with IMQ at day 4.
c) Disease severity of psoriasis induced by IMQ in mice as assessed by PASI score (n=7).
d) Representative images and statistical analysis of hematoxylin and eosin staining of the dorsal skin in control and GSDMD-cKO mice treated with IMQ at day 4 (n=5). Scale bar =100µm.
e) Quantitative PCR analysis of the relative mRNA expression of proinflammatory cytokines in the dorsal skin of control and GSDMD-cKO mice treated with IMQ at day 4 (n = 4). Data were normalized to a reference gene, Gapdh.
f) ELISA analysis of IL-6 and IL-1b per 1 mg of the dorsal skin from control and GSDMD-cKO mice treated with IMQ at day 4(n=5).
g) Representative images and statistical analysis of western blot analysis showing the expression level of GSDMD and its N-terminal fragments in dorsal skin of WT, cKO and Gsdmd-/- mice treated with IMQ at day 4 (n=4).
h) Schematic representation of the use of anti-Ly6G antibody in the IMQ-induced psoriasis mouse model.
i) Macroscopic phenotypic representation and PASI score of cKO mice and control mice treated with IMQ and Ly6G antibody.
cKO, conditional knockout. Error bars show mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001. Data are representative of three independent experiments for (a, b, d, g, i).