Figure 1: DC MST1 deficiency leads to spontaneous diseases.

(a) Kaplan–Meier plots of WT and Mst1^ΔDC mouse survival after birth are shown (n=20). (b) Body weights of the WT and Mst1^ΔDC mice after birth are summarized (n=20). (c) H&E staining of hepatic and intestinal tissues from sex- and age-matched WT and Mst1^ΔDC mice at 20 weeks after birth is presented. Scale bars, 100 μm. (d) DC MST1 deficiency leads to more CD44^highCD62L^low cells among CD4⁺T cells than WT control mice at 20 weeks after birth. Gating strategies for determining the percentage of CD4⁺TCR⁺CD44^highCD62L^low cells are showed in Supplementary Fig. 4C. Intracellular IL-17A and IFN-γ expression of CD4⁺T cells isolated from MLN, PP, IEL and LPL in WT and Mst1^ΔDC mice with a typical figure displayed (e) and the frequencies of positive cells summarized (f). Data are representative of three to four independent experiments (mean±s.d.; n=4). ***P<0.001, compared with the indicated groups. n.s., not significant. P-values were determined using Student’s t-tests.