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Partial Deficiency of Zfp217 Resists High-Fat Diet-Induced Obesity by Increasing Energy Metabolism in Mice.

Abstract
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.
AuthorsQianhui Zeng, Nannan Wang, Yaru Zhang, Yuxuan Yang, Shuangshuang Li, Rong Zheng, Jin Chai, Tong Qiao, Siwen Jiang
JournalInternational journal of molecular sciences (Int J Mol Sci) Vol. 22 Issue 10 (May 20 2021) ISSN: 1422-0067 [Electronic] Switzerland
PMID34065474 (Publication Type: Journal Article)
Chemical References
  • Trans-Activators
  • ZFP217 protein, mouse
Topics
  • Adipocytes, White (metabolism, physiology)
  • Adipogenesis (physiology)
  • Adipose Tissue, White (metabolism, physiopathology)
  • Animals
  • Diet, High-Fat
  • Energy Metabolism (physiology)
  • Fibroblasts (metabolism, physiology)
  • Insulin Resistance (physiology)
  • Lipid Metabolism (physiology)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Obese
  • Obesity (metabolism, physiopathology)
  • Thermogenesis (physiology)
  • Trans-Activators (metabolism)
  • Weight Gain (physiology)

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