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

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)...

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Veröffentlicht in:Biological & pharmaceutical bulletin 2017/06/01, Vol.40(6), pp.888-893
Hauptverfasser: Matsuo, Kohei, Matsusue, Kimihiko, Aibara, Daisuke, Takiguchi, Soichi, Gonzalez, Frank J., Yamano, Shigeru
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Sprache:eng
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Zusammenfassung: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.
ISSN:0918-6158
1347-5215
DOI:10.1248/bpb.b17-00105