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. 2015 Apr 10;6:6771. doi: 10.1038/ncomms7771

Figure 7. Haematopoietically derived cells acquire β-gal from LECs and induce Bg2 anergy.

Figure 7

(a) CTV-labelled Thy1.1+ Bg2 cells were transferred into the indicated recipients, along with CTV-labelled Thy1.1neg cells as an injection control. Proliferation in skin-draining LNs was measured 7 days later. Data representative of 1–2 experiments with 2–5 mice each. (b) CTV-labelled Thy1.1+ Bg2 cells were transferred into the indicated recipients, and Treg development was measured 3 days later. Data representative of 2 experiments with 2–3 mice each. (c) Experimental design to measure tolerance induction. CTV-labelled CD25negThy1.1+ Bg2 CD4 T cells were adoptively transferred, and recipient mice were challenged 28 days later with peptide-pulsed BMDCs. Proliferation was measured 5 days later by Ki67 upregulation, and FoxP3 and CD25 were measured to assess Treg formation. (d) Representative and (e) cumulative data gated on CD4+Thy1.1+ Bg2 cells from skin-draining LN from 2 experiments with 1–7 mice each. *P<0.05; **P<0.01; ***P<0.001, NS=not significant. Indicated comparisons were made using a one-way analysis of variance with Bonferroni post-test. All data shown as mean±s.e.m.