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. 2022 Aug 22;57(16):1922–1936.e9. doi: 10.1016/j.devcel.2022.07.014

Figure 3.

Figure 3

Modeling PTF1A enhancer mutations in human MPCs

(A) qRT-PCR of human MPCs for pancreatic progenitor markers (n = 7–13 independent differentiation experiments per genotype, using 6 PTF1AenhΔ/enhΔ clones—3 lines with 127 bp and 3 lines with 321-bp deletions, see Figure S2B—and 4 PTF1A+/+ control lines. Graphs show means ± SEM. Mann-Whitney p ≤ 0.05, ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001).

(B) Quantification of FACS data for PDX1+ NKX6-1+ stage-4 in vitro derived MPCs (n = 8–10 independent differentiation experiments per genotype; ns, not significant).

(C) Immunofluorescence of human MPCs (stage 4) shows absence of PTF1A in PTF1AenhΔ/enhΔ lines, without changes in NKX6-1. See also Figure S2.