Spiegelman B M
Department of Cancer Biology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
Diabetes. 1998 Apr;47(4):507-14. doi: 10.2337/diabetes.47.4.507.
The past several years have seen an explosive increase in our understanding of the transcriptional basis of adipose cell differentiation. In particular, a key role has been illustrated for PPAR-gamma, a member of the nuclear hormone receptor superfamily. PPAR-gamma has also been recently identified as the major functional receptor for the thiazolidinedione class of insulin-sensitizing drugs. This review examines the evidence that has implicated this transcription factor in the processes of adipogenesis and systemic insulin action. In addition, several models are discussed that may explain how a single protein can be involved in these related but distinct physiological actions. I also point out several important areas where our knowledge is incomplete and more research is needed. Finally, I discuss how advances in our understanding of nuclear receptor function, particularly the docking of cofactors in a ligand-dependent fashion, should lead to improved drugs that utilize the PPAR-gamma system for the treatment of insulin resistance.
在过去几年里,我们对脂肪细胞分化的转录基础的理解有了爆炸性的增长。特别是,核激素受体超家族成员PPAR-γ已被证明发挥关键作用。PPAR-γ最近还被确定为噻唑烷二酮类胰岛素增敏药物的主要功能受体。本综述考察了表明该转录因子参与脂肪生成和全身胰岛素作用过程的证据。此外,还讨论了几个模型,这些模型或许可以解释单一蛋白质如何参与这些相关但不同的生理作用。我还指出了几个我们的知识尚不完备、需要更多研究的重要领域。最后,我讨论了我们对核受体功能理解的进展,尤其是辅因子以配体依赖方式的对接,这应该会带来利用PPAR-γ系统治疗胰岛素抵抗的改良药物。