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. 2020 Jun 19;17:46. doi: 10.1186/s12986-020-00466-8

Fig. 5.

Fig. 5

Total mRNA was extracted from the livers of HFD-fed TET1-KO and WT mice and mRNA levels were determined by Q-PCR and normalized to β-actin. The mRNA of key genes for fatty acid oxidation in the liver of TET1-KO mice and WT mice and the L02 and HepG2 cells transfected with siRNA were detected by Q-PCR and normalized to β-actin (a,b,c). Western blot of PPARα, ACOX1, CPT1A and CD36 in TET1-KO mice and WT mice and the L02 and HepG2 cells transfected with siRNA (d,e,f). The content of β-HB in the plasma of TET1-KO mice and WT mice was fed by HFD. The content of β-HB in the supernatant of cells after transfection of siTET1 or control siRNA (f,g)