Avignone Elena, Lepleux Marilyn, Angibaud Julie, Nägerl U Valentin
Interdisciplinary Institute for Neurosciences, CNRS UMR 5297, 33077, Bordeaux, France.
Université de Bordeaux, CNRS UMR 5297, 33077, Bordeaux, France.
J Neuroinflammation. 2015 Nov 4;12:202. doi: 10.1186/s12974-015-0421-6.
Microglia cells are the resident macrophages of the central nervous system and are considered its first line of defense. In the normal brain, their ramified processes are highly motile, constantly scanning the surrounding brain tissue and rapidly moving towards sites of acute injury or danger signals. These microglial dynamics are thought to be critical for brain homeostasis. Under pathological conditions, microglial cells undergo "activation," which modifies many of their molecular and morphological properties. Investigations of the effects of activation on motility are limited and have given mixed results. In particular, little is known about how microglial motility is altered in epilepsy, which is characterized by a strong inflammatory reaction and microglial activation.
We used a mouse model of status epilepticus induced by kainate injections and time-lapse two-photon microscopy to image GFP-labeled microglia in acute hippocampal brain slices. We studied how microglial activation affected the motility of microglial processes, including basal motility, and their responses to local triggering stimuli.
Our study reveals that microglial motility was largely preserved in kainate-treated animals, despite clear signs of microglial activation. In addition, whereas the velocities of microglial processes during basal scanning and towards a laser lesion were unaltered 48 h after status epilepticus, we observed an increase in the size of the territory scanned by single microglial processes during basal motility and an elevated directional velocity towards a pipette containing a purinergic agonist.
Microglial activation differentially impacted the dynamic scanning behavior of microglia in response to specific acute noxious stimuli, which may be an important feature of the adaptive behavior of microglia during pathophysiological conditions.
小胶质细胞是中枢神经系统的常驻巨噬细胞,被认为是其第一道防线。在正常大脑中,它们的分支状突起具有高度的运动性,不断扫描周围的脑组织,并迅速移向急性损伤或危险信号部位。这些小胶质细胞的动态变化被认为对脑内稳态至关重要。在病理条件下,小胶质细胞会发生“激活”,这会改变它们的许多分子和形态学特性。关于激活对运动性影响的研究有限,结果也不一致。特别是,对于癫痫中小胶质细胞运动性如何改变知之甚少,癫痫的特征是强烈的炎症反应和小胶质细胞激活。
我们使用了由注射红藻氨酸诱导的癫痫持续状态小鼠模型,并通过延时双光子显微镜对急性海马脑片中绿色荧光蛋白标记的小胶质细胞进行成像。我们研究了小胶质细胞激活如何影响小胶质细胞突起的运动性,包括基础运动性以及它们对局部触发刺激的反应。
我们的研究表明,尽管有明显的小胶质细胞激活迹象,但在红藻氨酸处理的动物中,小胶质细胞的运动性在很大程度上得以保留。此外,虽然癫痫持续状态48小时后,小胶质细胞突起在基础扫描和朝向激光损伤处的速度未改变,但我们观察到单个小胶质细胞突起在基础运动期间扫描区域的大小增加,并且朝向含有嘌呤能激动剂的移液管的定向速度升高。
小胶质细胞激活对小胶质细胞响应特定急性有害刺激的动态扫描行为产生不同影响,这可能是病理生理条件下小胶质细胞适应性行为的一个重要特征。