Biospectrum Life Science Institute, Gunpo City, Gyunggi Do 435-833, Republic of Korea.
Cell Mol Life Sci. 2010 Feb;67(3):467-81. doi: 10.1007/s00018-009-0196-y. Epub 2009 Nov 26.
Adipocyte dysfunction is associated with the development of obesity. This study shows that 6-thioinosine inhibits adipocyte differentiation. The mRNA levels of PPAR gamma and C/EBPalpha, but not C/EBPbeta and delta, were reduced by 6-thioinosine. Moreover, the mRNA levels of PPAR gamma target genes (LPL, CD36, aP2, and LXRalpha) were down-regulated by 6-thioinosine. We also demonstrated that 6-thioinosine inhibits the transactivation activity and the mRNA level of PPAR gamma. Additionally, attempts to elucidate a possible mechanism underlying the 6-thioinosine-mediated effects revealed that 6-thioinosine induced iNOS gene expression without impacting eNOS expression, and that this was mediated through activation of AP-1, especially, JNK. In addition, 6-thioinosine was found to operate upstream of MEKK-1 in JNK activation signaling. Taken together, these findings suggest that the inhibition of adipocyte differentiation by 6-thioinosine occurs primarily through the reduced expression of PPAR gamma, which is mediated by upregulation of iNOS via the activation of JNK.
脂肪细胞功能障碍与肥胖的发生有关。本研究表明,6-硫代次黄嘌呤可抑制脂肪细胞分化。6-硫代次黄嘌呤可降低 PPARγ和 C/EBPα的 mRNA 水平,但不降低 C/EBPβ和δ的 mRNA 水平。此外,PPARγ靶基因(LPL、CD36、aP2 和 LXRα)的 mRNA 水平也被 6-硫代次黄嘌呤下调。我们还证明,6-硫代次黄嘌呤抑制 PPARγ的转录激活活性和 mRNA 水平。此外,为了阐明 6-硫代次黄嘌呤介导作用的可能机制,我们发现 6-硫代次黄嘌呤诱导 iNOS 基因表达而不影响 eNOS 表达,并且这种作用是通过激活 AP-1 特别是 JNK 介导的。此外,发现 6-硫代次黄嘌呤在 JNK 激活信号通路中作用于 MEKK-1 的上游。总之,这些发现表明,6-硫代次黄嘌呤通过降低 PPARγ的表达来抑制脂肪细胞分化,这是通过激活 JNK 上调 iNOS 介导的。