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. 2019 Mar 12;38(8):e100156. doi: 10.15252/embj.2018100156

Figure 2. Loss of Cideb protects mice from diet‐induced fatty liver diseases.

Figure 2

  • A
    Liver morphology of WT and Cideb −/− liver under chow diet and HFLF diet. H/E staining, oil red‐O staining, immunohistochemistry, and ultrastructure (Electron Microscope) were performed. Scale bar represented 50 μm in the upper three rows of images and 2 μm in the bottom row of images. LD: lipid droplet; ER: endoplasmic reticulum; M: mitochondrial; N: nucleus.
  • B, C
    Total liver TAG levels (B) and liver cholesterol ester levels (C) of WT and Cideb −/− mice under chow diet and HFLF diet (n = 8 per group).
  • D
    Loss of Cideb inhibits diet‐induced SREBP activation. IB of hepatic SREBP processing and lipogenic enzyme levels (Fasn, Scd1) of WT and Cideb −/− mice under chow diet and HFLF diet.
  • E
    Serum AST and ALT levels of WT and Cideb −/− mice under chow diet and HFLF diet (n = 8 per group).
  • F
    Cideb deficiency alleviates the whole body inflammation response. Serum TNFα, MCP1, and IL6 levels of WT and Cideb −/− mice under chow diet and HFLF diet (n = 8 per group).
  • G, H
    Serum fed glucose levels (G) and insulin levels (H) of WT and Cideb −/− mice under chow diet and HFLF diet (n = 8 per group).
  • I
    Glucose tolerance test (GTT) of WT and Cideb −/− mice under HFLF diet (n = 5 per group).
  • J
    Insulin tolerance test (ITT) of WT and Cideb −/− mice under HFLF diet (n = 5 per group).
Data information: Data represent Mean ± SEM; NS: not significant; *P < 0.05; **P < 0.01; ***P < 0.001, by 2‐tailed Student's t‐test.Source data are available online for this figure.