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. 2018 Aug 23;8:12692. doi: 10.1038/s41598-018-31179-x

Figure 3.

Figure 3

PTPN22 is dispensable for FcγR dependent immune complex binding, uptake and processing. (a) WT (white) or Ptpn22−/− (black) BMDCs were incubated with ova-AF488 ICs for 1 hour on ice. Cell surface ova-AF488 IC binding was determined by flow cytometry, gating on live, CD11c+, anti-rabbit+ singlets. n = 3–5 + s.d. (b) Combined ova-AF488 IC internalisation by WT (white) and Ptpn22−/− (black) BMDCs was determined by flow cytometry, gating on live, CD11c+, anti-rabbit- singlets. n = 3–5 ± s.d. (c) Representative flow cytometry plots showing ova-AF594:anti-ova coated bead internalisation and ova degradation by WT BMDCs over 0–7 hours at 37 °C. (d) Proportion of beads internalised by WT (white) and Ptpn22−/− (black) BMDCs that have degraded ova-AF594 on them (gated on single, anti-rabbit- beads). n = 3 ± s.d. (technical repeats, representative of 8 independent experiments). (e) Ova-AF594 geometric mean fluorescence intensity (GMFI) of beads internalised by WT (white) and Ptpn22−/− (black) BMDCs (gated on single, anti-rabbit- beads). n = 3 ± s.d. (technical repeats, representative of 8 independent experiments).