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. 2023 Jun 1;220(9):e20221751. doi: 10.1084/jem.20221751

Figure S2.

Figure S2.

Citrullination of NETs potentiates inflammatory bone destruction. (A and B) Representative TRAP-stained sections of gingival tissues with or without LIP (6 d) in WT (n = 5) and Padi4 KO (n = 5) mice. (A) TRAP-positive cells appear as purplish to dark red in the sections. Scale bars are 50 µm; representative image. (B) Quantification of osteoclasts per condition, number of osteoclast/bone surface (N/mm). (C–H) Flow cytometry analysis of mouse oral gingival tissues with or without LIP (18 h) in WT (n = 4) and Padi4 KO (n = 4) mice. Graph indicating absolute number of CD45+ (C), neutrophils (CD45+CD11b+CD11clow/medLy6G+; D), lymphoid DCs (CD11bCD11c+; E), myeloid DCs (CD11b+ CD11clow-med; F), MNPs (CD11b+CD11clow-medLy6GLy6Clow-highSSClow; G), and eosinophils (CD11b+CD11clow-medLy6GLy6Clow-neg SSChigh; H) per standardized tissue block. Data are representative of three (B–H) independent experiments. Graphs show the mean ± SEM. *P < 0.05, **P < 0.01, ****P < 0.0001. One-way ANOVA with Tukey’s multiple comparison test (B), unpaired t test (C–H).