Insulin Represses Fasting-Induced Expression of Hepatic Fat-Specific Protein 27

Biol Pharm Bull. 2017;40(6):888-893. doi: 10.1248/bpb.b17-00105.

Abstract

The fat-specific protein 27 (Fsp27) gene belongs to the cell death-inducing DNA fragmentation factor 45-like effector family. Fsp27 is highly expressed in adipose tissue as well as the fatty liver of ob/ob mice. Fsp27 is directly regulated by the peroxisome proliferator-activated receptor γ (PPARγ) in livers of genetically obese leptin deficient ob/ob mice. In the present study, Fsp27 was markedly induced by 24 h fasting in genetically normal mouse livers and repressed by refeeding a high sucrose diet. In contrast with the liver, Fsp27 expression was decreased in adipose tissue by fasting and increased by refeeding. Interestingly, fasting-induced Fsp27 liver expression was independent of PPARγ. Moreover, Fsp27 expression was induced in the insulin-depleted livers of streptozotocin-treated mice. Finally, Fsp27 expression was repressed by direct injection of glucose or insulin in fasting mice. These results suggest that insulin represses Fsp27 expression in the fasting liver.

Keywords: fat-specific protein 27 (Fsp27); fatty liver; insulin; peroxisome proliferator-activated receptor γ (PPARγ).

MeSH terms

  • Adipose Tissue, White / metabolism
  • Animals
  • Fasting / metabolism*
  • Insulin / pharmacology*
  • Liver / metabolism*
  • Male
  • Mice, Knockout
  • Mice, Obese
  • PPAR gamma / genetics
  • Proteins / genetics*
  • Streptozocin

Substances

  • Insulin
  • PPAR gamma
  • Proteins
  • fat-specific protein 27, mouse
  • Streptozocin