Inhibitory effect of a proline-to-alanine substitution at codon 12 of peroxisome proliferator-activated receptor-γ 2 on thiazolidinedione-induced adipogenesis

被引:185
作者
Masugi, J [1 ]
Tamori, Y [1 ]
Mori, H [1 ]
Koike, T [1 ]
Kasuga, M [1 ]
机构
[1] Kobe Univ, Sch Med, Dept Internal Med 2, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词
D O I
10.1006/bbrc.2000.2096
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Peroxisome proliferator-activated receptor-gamma (PPAR gamma) is a member of the nuclear hormone receptor superfamily of transcription factors and appears to be a key regulator of adipogenesis. Members of the thiazolidinedione class of insulin-sensitizing agents act as high-affinity ligands for PPAR gamma, indicating that PPAR gamma is also important in systemic insulin action, To determine whether Pro(12) --> Ala (P12A) mutation in PPAR gamma gene contributes to the development of obesity or insulin sensitivity, we examined the effects of the P12A mutation on the function of PPAR gamma by expression of the mutant protein in COS or 3T3-L1 cells. The abilities of the P12A mutant of PPAR gamma to mediate both transcriptional activation of a luciferase reporter gene construct containing the peroxisome proliferator response element and adipogenesis induced by a thiazolidinedione drug were reduced compared with those of the wild-type protein. These results suggest that the P12A, substitution in PPAR gamma gene may be associated with abnormalities of adipose tissue formation and insulin sensitivity. (C) 2000 Academic Press.
引用
收藏
页码:178 / 182
页数:5
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