| First Author | Zeng Q | Year | 2021 |
| Journal | Int J Mol Sci | Volume | 22 |
| Issue | 10 | PubMed ID | 34065474 |
| Mgi Jnum | J:307358 | Mgi Id | MGI:6720423 |
| Doi | 10.3390/ijms22105390 | Citation | Zeng Q, et al. (2021) Partial Deficiency of Zfp217 Resists High-Fat Diet-Induced Obesity by Increasing Energy Metabolism in Mice. Int J Mol Sci 22(10) |
| abstractText | Obesity-induced adipose tissue dysfunction and disorders of glycolipid metabolism have become a worldwide research priority. Zfp217 plays a crucial role in adipogenesis of 3T3-L1 preadipocytes, but about its functions in animal models are not yet clear. To explore the role of Zfp217 in high-fat diet (HFD)-induced obese mice, global Zfp217 heterozygous knockout (Zfp217(+/-)) mice were constructed. Zfp217(+/-) mice and Zfp217(+/+) mice fed a normal chow diet (NC) did not differ significantly in weight gain, percent body fat mass, glucose tolerance, or insulin sensitivity. When challenged with HFD, Zfp217(+/-) mice had less weight gain than Zfp217(+/+) mice. Histological observations revealed that Zfp217(+/-) mice fed a high-fat diet had much smaller white adipocytes in inguinal white adipose tissue (iWAT). Zfp217(+/-) mice had improved metabolic profiles, including improved glucose tolerance, enhanced insulin sensitivity, and increased energy expenditure compared to the Zfp217(+/+) mice under HFD. We found that adipogenesis-related genes were increased and metabolic thermogenesis-related genes were decreased in the iWAT of HFD-fed Zfp217(+/+) mice compared to Zfp217(+/-) mice. In addition, adipogenesis was markedly reduced in mouse embryonic fibroblasts (MEFs) from Zfp217-deleted mice. Together, these data indicate that Zfp217 is a regulator of energy metabolism and it is likely to provide novel insight into treatment for obesity. |
