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. 2019 Jul 25;116(33):16489–16496. doi: 10.1073/pnas.1900079116

Fig. 1.

Fig. 1.

SLAMF9 is expressed on pDCs and regulates their numbers. (A) Sorted pDCs (CD19CD11CinterB220+PDCA+), B cells (CD19+ B220+), and cDCs (CD19B220CD11B+CD11Chigh) were analyzed for the mRNA levels of SLAMF9. Graph shows relative expression of target gene/reference gene (L32). Results are represented as mean percentage ± SD (unpaired t test 2-tailed **P < 0.005, ***P < 0.0005); n = 3–8. (BD) SLAMF9 protein levels were analyzed under naïve state in pDCs (CD19CD11CinterB220+PDCA+ CD11B), B cells (CD19+ B220+), cDCs (CD19B220CD11B+CD11Chigh), and in macrophages (CD11B+CD11C CD19-SSClow). Graph shows protein levels in the BM (B), spleen (C), and in the LN (D). (E) DNA agarose gel electrophoresis demonstrating a genomic deletion of about 200 bp in 3 SLAMF9−/− mice compared with 3 WT controls. (FH) Representative FACS plots showing SLAMF9 expression in WT compared with SLAMF9−/− pDCs as a negative control. (F) SLAMF9 expression in the BM. (G) SLAMF9 expression in the spleen. (H) SLAMF9 expression in the LN. (I and J) LN pDCs (CD19CD11CinterB220+PDCA+) were analyzed in WT and SLAMF9−/− mice. (I) Representative dot plot. (J) Graph shows the percent of pDCs in the LN. Results are a summary of 6 independent experiment; n = 26 mice (unpaired t test 2-tailed *P < 0.05, **P < 0.005, ***P < 0.0005, ****P < 0.0001).