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. 2014 Apr 7;6(6):721–731. doi: 10.1002/emmm.201403943

Figure 4. Skeletal muscle of Deletor mice have enhanced mitochondrial unfolded protein response (UPRmt), expression of fatty acid oxidation enzymes, and deacetylation of FOXO1, a downstream target of Sirt1.

Figure 4

  • A Skeletal muscle, total FOXO1 (total-F), and acetylated FOXO1 (ac-F) protein levels. Western blot analysis, Deletor and WT mice, on CD or NR (n = 4 for each group); tubulin as a loading control.
  • B Quantification of acetylated FOXO1, from Western blot results (n = 4 in each group).
  • C Quantification of total FOXO1 (B), from Western blot results (n = 4 in each group).
  • D–F Muscle mRNA expression of fatty acid transport and oxidation proteins CD36, ACOX1, MCAD (post-manifestation Deletor NR n = 12; Deletor CD n = 11; WT NR n = 8; WT CD n = 7; arbitrary units).
  • G Muscle UPRmt proteins HSP70, HSP60, ClpP in post-manifestation Deletors, and WT mice on NR- or CD-fed diet. Western blot analysis, beta-actin as a loading control.
  • H Serum FGF21 in Deletors and WT mice on CD or NR diet, post-manifestation (Deletor NR n = 12; Deletor CD n = 11; WT NR n = 8; WT CD n = 7). ELISA analysis.

Data information: All values are presented as mean ± s.e.m. (Student's t-test).

Source data are available for this figure.