Department of Neurology, Medicine and Vanderbilt Kennedy Center, Vanderbilt University, Nashville, Tennessee 37232, USA.
J Neurosci. 2010 Apr 14;30(15):5242-52. doi: 10.1523/JNEUROSCI.6366-09.2010.
Ischemic preconditioning is a phenomenon in which low-level stressful stimuli upregulate endogenous defensive programs, resulting in subsequent resistance to otherwise lethal injuries. We previously observed that signal transduction systems typically associated with neurodegeneration such as caspase activation are requisite events for the expression of tolerance and induction of HSP70. In this work, we sought to determine the extent and duration of oxidative and energetic dysfunction as well as the role of effector kinases on metabolic function in preconditioned cells. Using an in vitro neuronal culture model, we observed a robust increase in Raf and p66(Shc) activation within 1 h of preconditioning. Total ATP content decreased by 25% 3 h after preconditioning but returned to baseline by 24 h. Use of a free radical spin trap or p66(shc) inhibitor increased ATP content whereas a Raf inhibitor had no effect. Phosphorylated p66(shc) rapidly relocalized to the mitochondria and in the absence of activated p66(shc), autophagic processing increased. The constitutively expressed chaperone HSC70 relocalized to autophagosomes. Preconditioned cells experience significant total oxidative stress measured by F(2)-isoprostanes and neuronal stress evaluated by F(4)-neuroprostane measurement. Neuroprostane levels were enhanced in the presence of Shc inhibitors. Finally, we found that inhibiting either p66(shc) or Raf blocked neuroprotection afforded by preconditioning as well as upregulation of HSP70, suggesting both kinases are critical for preconditioning but function in fundamentally different ways. This is the first work to demonstrate the essential role of p66(shc) in mediating requisite mitochondrial and energetic compensation after preconditioning and suggests a mechanism by which protein and organelle damage mediated by ROS can increase HSP70.
缺血预处理是一种现象,其中低水平的应激刺激上调内源性防御程序,导致随后对其他致命损伤的抵抗力。我们之前观察到,与神经退行性变相关的信号转导系统,如 caspase 激活,是耐受表达和 HSP70 诱导所必需的事件。在这项工作中,我们试图确定氧化和能量功能障碍的程度和持续时间,以及效应激酶在预处理细胞代谢功能中的作用。使用体外神经元培养模型,我们观察到预处理后 1 小时内 Raf 和 p66(Shc)的激活明显增加。预处理后 3 小时总 ATP 含量下降 25%,但 24 小时后恢复基线。使用自由基自旋捕获剂或 p66(shc)抑制剂可增加 ATP 含量,而 Raf 抑制剂则没有效果。磷酸化的 p66(shc)迅速重新定位到线粒体,在没有激活的 p66(shc)的情况下,自噬过程增加。组成型表达的伴侣蛋白 HSC70 重新定位到自噬体。通过 F(2)-异前列腺素测量预处理细胞经历显著的总氧化应激,通过 F(4)-神经前列腺素测量评估神经元应激。Shc 抑制剂存在时,神经前列腺素水平升高。最后,我们发现抑制 p66(shc)或 Raf 均可阻断预处理提供的神经保护作用以及 HSP70 的上调,这表明两种激酶对预处理都是至关重要的,但以根本不同的方式发挥作用。这是第一项证明 p66(shc)在介导预处理后的必需线粒体和能量补偿中起关键作用的工作,并提出了一种机制,即 ROS 介导的蛋白质和细胞器损伤可以增加 HSP70。