Nelson Ashley N, Calhoun Michael S, Thomas Ankur M, Tavares Jennifer L, Ferretti Daniel M, Dillon Gregory M, Mandelblat-Cerf Yael
Biogen, Cambridge, MA, United States.
Front Cell Neurosci. 2020 Dec 3;14:566789. doi: 10.3389/fncel.2020.566789. eCollection 2020.
Ischemic stroke is recognized as one of the leading causes of adult disability, morbidity, and death worldwide. Following stroke, acute neuronal excitotoxicity can lead to many deleterious consequences, one of which is the dysregulation of intracellular calcium ultimately culminating in cell death. However, to develop neuroprotective treatments that target neuronal excitotoxicity, it is essential to know the therapeutic time window for intervention following an ischemic event. To address this question, the current study aimed to characterize the magnitude and temporal progression of neuronal intracellular calcium observed following distal middle cerebral artery occlusion (dMCAO) in mice. Using the calcium fluorescence indicator, GCaMP, we tracked neuronal population response in freely moving animals immediately following dMCAO in both the core infarct and peri-infarct regions. Our results demonstrate that calcium excitotoxicity following artery occlusion can be generally characterized by two phases: a transient increase in activity that lasts tens of minutes, followed by a long, slow sustained increase in fluorescence signal. The first phase is primarily thought to represent neuronal hyperexcitability, defining our therapeutic window, while the second may represent gradual cell death. Importantly, we show that the level of intracellular calcium following artery occlusion correlated with the infarct size at 24 h demonstrating a direct connection between excitotoxicity and cell death in our stroke model. In addition, we show that administration of the NMDA antagonist MK-801 resulted in both a decrease in calcium signal and a subsequent reduction in the infarct size. Altogether, this study represents the first demonstration in freely moving animals characterizing the temporal progression of toxic calcium signaling following artery occlusion. In addition, these results define a critical time window for neuroprotective therapeutic intervention in mice.
缺血性中风被认为是全球范围内成年人残疾、发病和死亡的主要原因之一。中风后,急性神经元兴奋性毒性会导致许多有害后果,其中之一是细胞内钙调节失调,最终导致细胞死亡。然而,要开发针对神经元兴奋性毒性的神经保护治疗方法,了解缺血事件后干预的治疗时间窗至关重要。为了解决这个问题,当前的研究旨在描述小鼠大脑中动脉远端闭塞(dMCAO)后观察到的神经元细胞内钙的变化幅度和时间进程。使用钙荧光指示剂GCaMP,我们追踪了dMCAO后自由活动动物在核心梗死区和梗死周围区域的神经元群体反应。我们的结果表明,动脉闭塞后的钙兴奋性毒性通常可分为两个阶段:持续数十分钟的短暂活性增加,随后是荧光信号的长时间缓慢持续增加。第一阶段主要被认为代表神经元的过度兴奋,这确定了我们的治疗窗口,而第二阶段可能代表逐渐的细胞死亡。重要的是,我们表明动脉闭塞后细胞内钙的水平与24小时后的梗死面积相关,这表明在我们的中风模型中兴奋性毒性与细胞死亡之间存在直接联系。此外,我们表明给予NMDA拮抗剂MK-801可导致钙信号降低以及随后梗死面积减小。总之,这项研究首次在自由活动的动物中描述了动脉闭塞后有毒钙信号的时间进程。此外,这些结果确定了小鼠神经保护治疗干预的关键时间窗。