Fig. 3: Adipocyte-specific knockout of KLF10 (KLF10AKO) impairs exercise-induced browning and lipid catabolism in male mice. | Nature Communications

Fig. 3: Adipocyte-specific knockout of KLF10 (KLF10AKO) impairs exercise-induced browning and lipid catabolism in male mice.

From: Exercise-induced anti-obesity effects in male mice generated by a FOXO1-KLF10 reinforcing loop promoting adipose lipolysis

Fig. 3

Chow diet (CD) fed KLF10AKO and wild type (WT) control male mice were subjected to treadmill training (Ex) or kept sedentary lifestyle (Sed) for 8 weeks before being sacrificed for analysis. a The treadmill exercise program is illustrated. The graph model was created in BioRender. Zhu, J. (2025) https://BioRender.com/z12f220. b Representative images of hematoxylin and eosin (H&E) staining of adipose tissues. Scale bars, 100 μm. Quantification of adipocyte diameter in iWAT and eWAT was shown below. c Immunohistochemistry (IHC) staining of UCP1 in iWAT and BAT. Scale bars, 50 μm. d The mRNA levels of the indicated genes in iWAT. Data were normalized to the WT/Sed group. e, f After 7 weeks of exercise training, the serum free fatty acid (FFA) and glycerol levels of CD-fed mice under 22 °C or 4 °C condition for 12 h. g The mRNA levels of the indicated genes in iWAT and eWAT. Data were normalized to the WT/Sed group. h, i Representative western blotting of iWAT and eWAT lysates. β-tubulin serves as an internal control. For statistical analysis, two-way ANOVA plus Tukey’s post hoc tests were performed in b, d, g; three-way ANOVA plus Tukey’s post hoc tests were performed in e, f. n = 6 male mice per group in all the above experiments. All data show the means ± SD. Source data are provided as a Source Data file.

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