Department of Biochemistry and Molecular Biology, Osaka University Graduate School of Medicine, Osaka, Japan.
Biochem Biophys Res Commun. 2012 Oct 12;427(1):100-6. doi: 10.1016/j.bbrc.2012.09.017. Epub 2012 Sep 13.
Axon degeneration is a hallmark of many neurological disorders, including Alzheimer's disease, motor neuron disease, and nerve trauma. Multiple factors trigger axon degeneration, and glutamate excitotoxicity is one of them. We have recently found that stabilization of microtubules and components of the dynein-dynactin complex modulate the process of excitotoxicity-induced axon degeneration. However, the molecular mechanisms involving these microtubule-based functions remain poorly understood. Here, we used hippocampal cultures and find that inhibition of p53 transactivation and microtubule stabilization function cooperatively to suppress excitotoxicity-induced mitochondrial dysfunction. Inhibition of p53 association with mitochondria has no effect on excitotoxicity-induced mitochondrial dysfunction, however, induces axon degeneration in normal condition. Association of p150Glued with mitochondria is significantly increased by simultaneously inhibiting p53 transactivation and microtubule stabilization under excitotoxic condition. Importantly, we find that inhibition of p53 transactivation and microtubule stabilization function cooperatively to suppress excitotoxicity-induced axon degeneration. Overexpression of p150Glued does not improve the effect by inhibition of p53 transactivation on axon degeneration suggesting that p150Glued and p53 function in a linear pathway in the process of axon degeneration.
轴突变性是许多神经疾病的标志,包括阿尔茨海默病、运动神经元疾病和神经创伤。多种因素引发轴突变性,其中谷氨酸兴奋性毒性是其中之一。我们最近发现,微管的稳定和动力蛋白-动力蛋白复合物的成分调节兴奋性毒性诱导的轴突变性过程。然而,涉及这些基于微管的功能的分子机制仍知之甚少。在这里,我们使用海马培养物发现,抑制 p53 反式激活和微管稳定功能协同作用以抑制兴奋性毒性诱导的线粒体功能障碍。抑制 p53 与线粒体的关联对兴奋性毒性诱导的线粒体功能障碍没有影响,但在正常情况下会诱导轴突变性。在兴奋性条件下同时抑制 p53 反式激活和微管稳定,p150Glued 与线粒体的结合显著增加。重要的是,我们发现抑制 p53 反式激活和微管稳定功能协同作用以抑制兴奋性毒性诱导的轴突变性。p150Glued 的过表达并不能改善抑制 p53 反式激活对轴突变性的作用,这表明 p150Glued 和 p53 在轴突变性过程中在一条线性途径中发挥作用。