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. Author manuscript; available in PMC: 2021 Nov 17.
Published in final edited form as: Nat Metab. 2021 May 17;3(5):604–617. doi: 10.1038/s42255-021-00389-5

Extended Data Figure 5: Assessment of UCP1/SUCNR1KO during WD and succinate drinking water experiments.

Extended Data Figure 5:

a, Representative cytofluorimetric dot plots for indicated immune cell populations from livers of WT, UCP1KO and UCP1/SUCNR1KO mice following 14 weeks on WD.

b, Relative gene expression in WT, UCP1KO, and UCP1/SUCNR1KO livers following 14 weeks WD feeding (n = 10 except Il6, Nos2 n = 9 in WT and Nos2 n = 9 in UCP1/SUCNR1KO).

c, Fraction of CD45+ cells for each indicated gated cell population from livers of WT, UCP1KO and UCP1/SUCNR1KO mice following 14 weeks on WD (n = 9 except CD8 n = 7 in UCP1/SUCNR1KO).

d-h, Protein abundance differences of annotated pathways proteins or HSC activation proteins between vehicle and 1.5% succinate-treated UCP1KO liver following 6 weeks HFD (n = 3). Data represent fold over 0%.

i, Sirius red staining observed in liver harvested from mice following 14 weeks WD feeding (upper panels 20x magnification, scale bars 100 μm; middle panels, 10x magnification, scale bars 200 μm, lower panels, 4x magnification, scale bars 200 μm; n = 4 biological replicates/genotype imaged).

j, Relative abundance of hydroxyproline in plasma following 14 weeks on WD WT (n = 10).

*P < 0.05, **P<0.01, ***P<0.001. (two-tailed Student’s t-test for pairwise comparisons, one-way ANOVA for multiple comparisons involving independent variable). Data are mean ± s.e.m. Assessments of UCP1/SUCNR1KO mice were performed simultaneously with WT and UCP1KO as depicted in Figure 2 and Extended Data Figure 2, so WT and UCP1KO presentations in this figure are from the same underlying data reported in Figure 2 and Extended Data Figure 2. See source data for precise p values.