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. 2020 Jul 14;32(2):107894. doi: 10.1016/j.celrep.2020.107894

Figure 2.

Figure 2

T Cells Are Activated When Co-cultured with Autologous ER-Stressed iPSC-β

(A) Experimental design: PBMCs co-cultured with autologous iPSC-β.

(B–D) Flow cytometry data of T cells after a 4-8h co-culture with iPSC-β cells (n = 3 T1D and n = 1 ND donor, n = 3 differentiation batches per donor line). T1D1, T1D2, and T1D3 were pooled together.

(B) CD25+ and (C) CD69+ co-positive for CD3+, CD4+, or CD8+ cells, as indicated. The values are represented as adjusted MFI.

(D) Pro-inflammatory cytokine detection in supernatants collected after 48 h co-culture of PBMC with iPSC-β (n = 3 T1D and n = 1 ND donor, n = 3 differentiation batches per donor line). T1D1, T1D2, and T1D3 were pooled together.

(E) Percentage of live iPSC-β after co-culture, gated for C-peptide+/glucagon (n = 3 T1D and n = 1 ND donor, n = 3 differentiation batches per donor line). T1D1, T1D2, and T1D3 were pooled together.

p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.0005, and ∗∗∗∗p < 0.0001. Ordinary 1-way ANOVA. ns, non-significant. See also Figure S2.