Fig. 1
From: Sex- and species-specific contribution of CD99 to T cell costimulation during multiple sclerosis

Increased CD99 expression in immune cells from men. A Sex-specific differentially expressed (pseudo)autosomal genes in spleen samples (n = 87 women and 154 men) from the Genotype-Tissue Expression (GTEx) dataset. B, C Corresponding mRNA expression levels of CD99, SRY and XIST in spleen. D CD99 surface protein expression on subsets of cryoconserved peripheral blood mononuclear cells (PBMCs) from male (n = 30) and female (n = 30) healthy individuals as analyzed by flow cytometry. Cell subsets were identified as following: CD4+ and CD8+ memory (gated as living CD3+-CD4+/CD8+-CD45RA– cells) and naïve (gated as living CD3+-CD4+/CD8+-CD45RA+ cells) T cells; pDCs (gated as living CD45+-Lineage(CD3, CD14, CD19, CD20, CD56)–-HLA-DR+-CD11c–-CD123+-CD304+ cells); cDCs (gated as living CD45+-Lineage(CD3, CD14, CD19, CD20, CD56)–-HLA-DR+-CD11c+ cells); B cells (gated as living CD45+- CD19+-CD20+ cells); NK cells (gated as living CD45+- CD19–-CD20–-CD3–-CD14–-CD56+ cells) and monocytes (gated as living CD45+- CD19–-CD20–-CD3–-CD14+ cells). E Representative flow cytometry plots of CD99 surface expression on immune cells shown in (D). Data are shown as violin plots including median. Statistics: A–C DESeq2 false discovery rate-adjusted P value; D two-way ANOVA with Tukey post-hoc; *P < 0.05; **P < 0.01; ***P < 0.001