Mizukami J, Taniguchi T
Lead Generation Research Laboratory, Tanabe Seiyaku Co., Ltd., Osaka, Japan.
Biochem Biophys Res Commun. 1997 Nov 7;240(1):61-4. doi: 10.1006/bbrc.1997.7602.
The peroxisome proliferator-activated receptor (PPAR) gamma is a member of the nuclear hormone receptor family, which is predominantly expressed on adipocytes and considered to be involved in the process of adipogenesis. The new thiazolidinedione (TZD) compound, T-174, developed as an antidiabetic drug, stimulated the transcription of PPAR gamma and the adipocyte differentiation of 3T3-L1 cells. Interestingly, T-174 induced the interaction between PPAR gamma and CBP (cAMP response element binding protein (CREB) binding protein), a co-factor of various transcription regulators. CBP mRNA was expressed in both preadipocytes and adipocytes. These results suggest that CBP plays a role in the PPAR gamma-mediated signaling pathway activated by TZD, including adipogenesis.
过氧化物酶体增殖物激活受体(PPAR)γ是核激素受体家族的成员,主要在脂肪细胞中表达,并被认为参与脂肪生成过程。作为一种抗糖尿病药物开发的新型噻唑烷二酮(TZD)化合物T-174,刺激了PPARγ的转录以及3T3-L1细胞的脂肪细胞分化。有趣的是,T-174诱导了PPARγ与CBP(环磷酸腺苷反应元件结合蛋白(CREB)结合蛋白)之间的相互作用,CBP是各种转录调节因子的辅助因子。CBP mRNA在前脂肪细胞和脂肪细胞中均有表达。这些结果表明,CBP在由TZD激活的包括脂肪生成在内的PPARγ介导的信号通路中发挥作用。