Department of Neurobiology, Kyoto Pharmaceutical University, Kyoto 607-8414, Japan.
Department of Molecular Cell Biology, Interdisciplinary Graduate School of Medicine and Engineering, University of Yamanashi, Chuo 409-3898, Japan.
Int J Mol Sci. 2009 Nov 5;10(11):4789-4804. doi: 10.3390/ijms10114789.
Although a loss-of-function mutation has been 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 identified UCP0045037 as a compound that bound to the reduced form of DJ-1 by in silico virtual screening. In this study, we determined the neuroprotective effects of UCP0045037 against focal cerebral ischemia-induced neurodegeneration in rats. Hydrogen peroxide-induced cell death was significantly inhibited by UCP0045037 in both rat mesencephalic dopaminergic neurons and human normal SH-SY5Y cells. In contrast, DJ-1-knockdown SH-SY5Y cells lost the protective activity of UCP0045037. These results suggest that UCP0045037 interacts with endogenous DJ-1 and produces a neuroprotective response.
虽然在家族性帕金森病 PARK7 中已经鉴定出功能丧失突变,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鉴定出 UCP0045037 是一种与 DJ-1 的还原形式结合的化合物。在这项研究中,我们确定了 UCP0045037 对大鼠局灶性脑缺血诱导的神经退行性变的神经保护作用。UCP0045037 显著抑制了过氧化氢诱导的大鼠中脑多巴胺能神经元和人正常 SH-SY5Y 细胞的细胞死亡。相比之下,DJ-1 敲低的 SH-SY5Y 细胞丧失了 UCP0045037 的保护活性。这些结果表明,UCP0045037 与内源性 DJ-1 相互作用并产生神经保护反应。