Yanagida Takashi, Kitamura Yoshihisa, Yamane Koichiro, Takahashi Kazunori, Takata Kazuyuki, Yanagisawa Daijiro, Yasui Hiroyuki, Taniguchi Takashi, Taira Takahiro, Honda Toshio, Ariga Hiroyoshi
Department of Neurobiology, Kyoto Pharmaceutical University, Japan.
J Pharmacol Sci. 2009 Mar;109(3):463-8. doi: 10.1254/jphs.08323sc. Epub 2009 Mar 11.
Although a loss-of-function type mutation was identified in familial Parkinson's disease PARK7, the wild-type of DJ-1 is known to act as an oxidative stress sensor in neuronal cells. Recently, we found a DJ-1 modulator UCP0054278 by in silico virtual screening. In this study, we determined the neuroprotective effects of UCP0054278 against focal ischemia-induced neurodegeneration in rats. Hydrogen peroxide-induced cell death and the production of reactive oxygen species were significantly inhibited by UCP0054278 in normal SH-SY5Y cells, but not in DJ-1-knockdown cells. These results suggest that UCP0054278 interacts with endogenous DJ-1 and then exhibits antioxidant and neuroprotective responses.
虽然在家族性帕金森病PARK7中鉴定出功能丧失型突变,但已知DJ-1的野生型在神经元细胞中作为氧化应激传感器发挥作用。最近,我们通过计算机虚拟筛选发现了一种DJ-1调节剂UCP0054278。在本研究中,我们确定了UCP0054278对大鼠局灶性缺血诱导的神经退行性变的神经保护作用。在正常的SH-SY5Y细胞中,UCP0054278可显著抑制过氧化氢诱导的细胞死亡和活性氧的产生,但在DJ-1基因敲低的细胞中则无此作用。这些结果表明,UCP0054278与内源性DJ-1相互作用,然后表现出抗氧化和神经保护反应。