Department of Neurology and Committee on Neurobiology, The University of Chicago Medical Center, Chicago, Illinois, United States of America.
PLoS One. 2011 Apr 26;6(4):e19294. doi: 10.1371/journal.pone.0019294.
Spreading depression (SD) is thought to cause migraine aura, and perhaps migraine, and includes a transient loss of synaptic activity preceded and followed by increased neuronal excitability. Activated microglia influence neuronal activity and play an important role in homeostatic synaptic scaling via release of cytokines. Furthermore, enhanced neuronal function activates microglia to not only secrete cytokines but also to increase the motility of their branches, with somata remaining stationary. While SD also increases the release of cytokines from microglia, the effects on microglial movement from its synaptic activity fluctuations are unknown. Accordingly, we used time-lapse imaging of rat hippocampal slice cultures to probe for microglial movement associated with SD. We observed that in uninjured brain whole microglial cells moved. The movements were well described by the type of Lévy flight known to be associated with an optimal search pattern. Hours after SD, when synaptic activity rose, microglial cell movement was significantly increased. To test how synaptic activity influenced microglial movement, we enhanced neuronal activity with chemical long-term potentiation or LPS and abolished it with TTX. We found that microglial movement was significantly decreased by enhanced neuronal activity and significantly increased by activity blockade. Finally, application of glutamate and ATP to mimic restoration of synaptic activity in the presence of TTX stopped microglial movement that was otherwise seen with TTX. Thus, synaptic activity retains microglial cells in place and an absence of synaptic activity sends them off to influence wider expanses of brain. Perhaps increased microglial movements after SD are a long-lasting, and thus maladaptive, response in which these cells increase neuronal activity via contact or paracrine signaling, which results in increased susceptibility of larger brain areas to SD. If true, then targeting mechanisms that retard activity-dependent microglial Lévy flights may be a novel means to reduce susceptibility to migraine.
扩散性抑制(SD)被认为会引起偏头痛先兆,甚至可能引起偏头痛,其特征是短暂的突触活动丧失,随后是神经元兴奋性增加。激活的小胶质细胞影响神经元活动,并通过释放细胞因子在稳态突触缩放中发挥重要作用。此外,增强的神经元功能激活小胶质细胞,不仅使其分泌细胞因子,而且增加其分支的运动性,而胞体保持静止。虽然 SD 也会增加小胶质细胞释放细胞因子,但它对小胶质细胞运动的影响与其突触活动波动有关尚不清楚。因此,我们使用大鼠海马切片培养物的延时成像来探测与 SD 相关的小胶质细胞运动。我们观察到,在未受伤的大脑中,整个小胶质细胞都在移动。这些运动很好地描述了与最佳搜索模式相关的已知的 Lévy 飞行类型。在 SD 数小时后,当突触活动增加时,小胶质细胞的运动显著增加。为了测试突触活动如何影响小胶质细胞的运动,我们通过化学长时程增强或 LPS 增强神经元活动,并通过 TTX 消除它。我们发现,神经元活动增强会显著降低小胶质细胞的运动,而活动阻断会显著增加小胶质细胞的运动。最后,应用谷氨酸和 ATP 来模拟 TTX 存在下的突触活动恢复会停止 TTX 引起的小胶质细胞运动。因此,突触活动使小胶质细胞保持在原位,而缺乏突触活动会使它们离开去影响大脑的更广泛区域。也许 SD 后小胶质细胞运动的增加是一种持久的、因此是适应不良的反应,其中这些细胞通过接触或旁分泌信号传递来增加神经元活动,从而导致更大脑区对 SD 的敏感性增加。如果这是真的,那么靶向减缓与活动相关的小胶质细胞 Lévy 飞行的机制可能是降低偏头痛易感性的一种新方法。