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Publication : Fat-specific protein 27b is regulated by hepatic peroxisome proliferator-activated receptor γ in hepatic steatosis.

First Author  Aibara D Year  2020
Journal  Endocr J Volume  67
Issue  1 Pages  37-44
PubMed ID  31564684 Mgi Jnum  J:297975
Mgi Id  MGI:6479470 Doi  10.1507/endocrj.EJ19-0296
Citation  Aibara D, et al. (2020) Fat-specific protein 27b is regulated by hepatic peroxisome proliferator-activated receptor gamma in hepatic steatosis. Endocr J 67(1):37-44
abstractText  The fat-specific protein 27 gene (Fsp27) belongs to the cell death-inducing DNA fragmentation factor 45-like effector family. Fsp27 is highly expressed in adipose tissue and fatty liver. In adipocytes, FSP27 localizes to the membrane of lipid droplets and promotes lipid droplet hypertrophy. Recently, FSP27 was shown to consist of two isoforms, FSP27alpha and FSP27beta. Previously, we demonstrated that Fsp27a is directly regulated by peroxisome proliferator-activated receptor gamma (PPARgamma) in fatty livers of genetically obese leptin deficient ob/ob mice and that Fsp27b may potentially be regulated by different factors transcriptionally as they both have a different promoter region. Thus, the aim of the present study was to elucidate whether Fsp27b is regulated by PPARgamma in fatty liver. Fsp27a and Fsp27b were markedly induced in fatty liver of ob/ob mice compared with those in the normal liver. However, both Fsp27a/b were expressed at markedly lower levels in liver-specific PPARgamma knockout mice with an ob/ob background. Further, the PPAR response element (PPRE) for the PPARgamma-dependent promotion of Fsp27b promotor activity was revealed at position -1,163/-1,151 from the transcriptional start site (+1). Interestingly, the cis-element responsible for the PPARgamma-dependent induction of Fsp27b was the same as that responsible for PPARgamma-dependent induction of Fsp27a. These results suggest that PPARgamma regulates not only Fsp27a but also Fsp27b in fatty liver of ob/ob mice through a common PPRE.
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