Extended Data Fig. 5: The development of homeostatic eTregs is not dependent on PD-1, and eTregs are limited by PD-1. | Nature Immunology

Extended Data Fig. 5: The development of homeostatic eTregs is not dependent on PD-1, and eTregs are limited by PD-1.

From: PD-L1–PD-1 interactions limit effector regulatory T cell populations at homeostasis and during infection

Extended Data Fig. 5

(a-f) Splenocytes from naïve 8 week-old female C57BL/6 mice or total PD-1−/− mice were isolated and analyzed via high-parameter flow cytometry. (a) Pre-gated CD4+ T cells gated on Foxp3+ events (Treg cells) depicting an enrichment of Treg cells at homeostasis in PD-1−/− age matched hosts (n = 3/group two-tailed unpaired student’s t-test, ** = p = 0.0037, 4 experimental replicates). (b) Comparative flow plots of Treg cells between C57BL/6 and PD-1−/− hosts with gating on activated Treg cells in cell cycle (CD11ahi Ki67+), demonstrating an increase in Tregs cells undergoing proliferation at homeostasis in PD-1−/− hosts (n = 3/group two-tailed unpaired student’s t-test, ** = p = 0.0044, 4 experimental replicates). (c) Treg cell staining of ICOS and CTLA-4, depicting the proportion and number of eTreg-associated (ICOS+ CTLA-4hi) Treg cells is increased in PD-1−/− mice (n = 3/group two-tailed unpaired student’s t-test, ** = p = 0.0022, 4 experimental replicates), while (d) demonstrates this enhancement is specific to the eTreg compartment (BCL-2low, CD25low), as the non-eTreg compartment (BCL-2hi, CD25hi) is consistent in number when compared to C57BL/6 mice (n = 5/group, 2-way ANOVA with Sidak’s multiple comparisons test, *** = p = 0.0001, 3 experimental replicates). Splenocytes from isotype and anti-PD-L1 treated groups were also stimulated and stained for IL-10 and analyzed via flow cytometry. (e) Flow plots of Treg cells from C57BL/6 and PD-1−/− hosts gated on CD11ahi IL-10+ events, depicting an increase in the proportion and number of IL-10+ Treg cells in PD-1-/- hosts (n = 3/group two-tailed unpaired student’s t-test, ** = p = 0.0011, 3 experimental replicates). (f) Splenic cDC2 subsets were identified via flow cytometry (CD3, B220, CD19, NK1.1, Ly6G, CD64, CD11c+, MHC-II+, SIRPα+), and gated on CD80+ events based on an FMO (n = 4/group, two-tailed unpaired student’s t test, * = p = 0.0122, 2 experimental replicates). All data presented are means + /- SEM and show individual data points.

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