Samarasinghe Shanika P, Sutanto Maria M, Danos Arpad M, Johnson Daniel N, Brady Matthew J, Cohen Ronald N
Section of Endocrinology, Department of Medicine, The University of Chicago, Chicago, Illinois, USA.
Obesity (Silver Spring). 2009 May;17(5):965-72. doi: 10.1038/oby.2008.629. Epub 2009 Jan 22.
Peroxisome proliferator-activated receptor gamma (PPARgamma) acts as a ligand-dependent transcription factor with a key role in mediating adipocyte differentiation and insulin sensitivity. Recently, we and others have shown that PPARgamma recruits the nuclear corepressors NCoR and silencing mediator for retinoid and thyroid hormone receptors (SMRT) to modulate adipogenesis. While the synthetic ligands for PPARgamma, the thiazolidinediones (TZD), are widely used in the treatment of type 2 diabetes mellitus, the biologically relevant endogenous PPARgamma ligand involved in adipogenesis remains unidentified. To further understand the role of ligand binding and corepressor interaction in PPARgamma-mediated adipogenesis, a mutation was introduced in the ligand-binding domain (LBD) of murine PPARgamma. PPARgammamut was created via two amino acid substitutions known to be major determinants of ligand selectivity among PPAR isotypes, H323Y and R288M. These mutations alter PPARgamma to the corresponding residues of the PPARalpha. Characterizing the in vitro functional properties of this mutant, we show that PPARgammamut preferentially responds to the PPARalpha agonist, WY-14643, over the TZD, pioglitazone. When expressed in 3T3-L1 preadipocytes using recombinant adenovirus, wild-type PPARgamma leads to adipocyte formation with both hormonal and TZD treatment. PPARgammamut blocks the upregulation of adipocyte-specific proteins by TZD, but surprisingly, not by standard hormonal inducers. Our data suggest that TZDs and the purported endogenous ligand do not interact in the same way with the PPARgamma LBD. We propose that the endogenous ligand has distinct properties that allow for promiscuity within the hydrophobic PPAR ligand-binding pocket, yet fosters appropriate cofactor recruitment and release to allow adipogenesis to proceed.
过氧化物酶体增殖物激活受体γ(PPARγ)作为一种依赖配体的转录因子,在介导脂肪细胞分化和胰岛素敏感性方面发挥关键作用。最近,我们和其他人已经表明,PPARγ招募核共抑制因子NCoR和视黄酸及甲状腺激素受体沉默介质(SMRT)来调节脂肪生成。虽然PPARγ的合成配体噻唑烷二酮类(TZD)被广泛用于治疗2型糖尿病,但参与脂肪生成的生物学相关内源性PPARγ配体仍未确定。为了进一步了解配体结合和共抑制因子相互作用在PPARγ介导的脂肪生成中的作用,在小鼠PPARγ的配体结合域(LBD)中引入了一个突变。通过已知是PPAR亚型中配体选择性主要决定因素的两个氨基酸取代(H323Y和R288M)创建了PPARgammamut。这些突变使PPARγ变为PPARα的相应残基。在表征该突变体的体外功能特性时,我们表明PPARgammamut优先对PPARα激动剂WY-14643作出反应,而不是对TZD吡格列酮作出反应。当使用重组腺病毒在3T3-L1前脂肪细胞中表达时,野生型PPARγ在激素和TZD处理下均导致脂肪细胞形成。PPARgammamut阻断了TZD对脂肪细胞特异性蛋白的上调,但令人惊讶的是,标准激素诱导剂并未使其阻断。我们的数据表明,TZD和所谓的内源性配体与PPARγ LBD的相互作用方式不同。我们提出,内源性配体具有独特的特性,允许在疏水性PPAR配体结合口袋内具有混杂性,但促进适当的辅因子募集和释放,以使脂肪生成得以进行。