Tatsumi Kouko, Okuda Hiroaki, Morita-Takemura Shoko, Tanaka Tatsuhide, Isonishi Ayami, Shinjo Takeaki, Terada Yuki, Wanaka Akio
Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical University Kashihara, Japan.
Department of Anatomy and Neuroscience, Faculty of Medicine, Nara Medical UniversityKashihara, Japan; Department of Functional Anatomy, Graduate School of Medical Sciences, Kanazawa UniversityKanazawa, Japan.
Front Cell Neurosci. 2016 Jun 21;10:165. doi: 10.3389/fncel.2016.00165. eCollection 2016.
Changes in astrocyte morphology are primarily attributed to the fine processes where intimate connections with neurons form the tripartite synapse and participate in neurotransmission. Recent evidence has shown that neurotransmission induces dynamic synaptic remodeling, suggesting that astrocytic fine processes may adapt their morphologies to the activity in their environment. To illustrate such a neuron-glia relationship in morphological detail, we employed a double transgenic Olig2(CreER/WT); ROSA26-GAP43-EGFP mice, in which Olig2-lineage cells can be visualized and traced with membrane-targeted GFP. Although Olig2-lineage cells in the adult brain usually become mature oligodendrocytes or oligodendrocyte precursor cells with NG2-proteoglycan expression, we found a population of Olig2-lineage astrocytes with bushy morphology in several brain regions. The globus pallidus (GP) preferentially contains Olig2-lineage astrocytes. Since the GP exerts pivotal motor functions in the indirect pathway of the basal ganglionic circuit, we subjected the double transgenic mice to voluntary wheel running to activate the GP and examined morphological changes of Olig2-lineage astrocytes at both the light and electron microscopic levels. The double transgenic mice were divided into three groups: control group mice were kept in a cage with a locked running wheel for 3 weeks, Runner group were allowed free access to a running wheel for 3 weeks, and the Runner-Rest group took a sedentary 3-week rest after a 3-week running period. GFP immunofluorescence analysis and immunoelectron microscopy revealed that astrocytic fine processes elaborated complex arborization in the Runner mice, and reverted to simple morphology comparable to that of the Control group in the Runner-Rest group. Our results indicated that the fine processes of the Olig2-lineage astrocytes underwent plastic changes that correlated with overall running activities, suggesting that they actively participate in motor functions.
星形胶质细胞形态的变化主要归因于其精细突起,这些突起与神经元形成紧密连接,构成三联突触并参与神经传递。最近的证据表明,神经传递会诱导动态突触重塑,这表明星形胶质细胞的精细突起可能会根据其周围环境的活动来调整自身形态。为了从形态学细节上阐明这种神经元-胶质细胞的关系,我们使用了双转基因Olig2(CreER/WT);ROSA26-GAP43-EGFP小鼠,其中Olig2谱系细胞可以通过膜靶向绿色荧光蛋白进行可视化和追踪。尽管成年大脑中的Olig2谱系细胞通常会成为表达NG2蛋白聚糖的成熟少突胶质细胞或少突胶质前体细胞,但我们在几个脑区发现了一群具有浓密形态的Olig2谱系星形胶质细胞。苍白球(GP)中优先含有Olig2谱系星形胶质细胞。由于GP在基底神经节回路的间接通路中发挥关键的运动功能,我们让双转基因小鼠进行自愿轮转跑步以激活GP,并在光学和电子显微镜水平上检查Olig2谱系星形胶质细胞的形态变化。双转基因小鼠分为三组:对照组小鼠被关在装有锁定转轮的笼子里3周,跑步组小鼠可以自由使用转轮3周,跑步-休息组小鼠在3周的跑步期后进行3周的久坐休息。绿色荧光蛋白免疫荧光分析和免疫电子显微镜显示,跑步组小鼠中星形胶质细胞的精细突起形成了复杂的分支,而在跑步-休息组中则恢复为与对照组相当的简单形态。我们的结果表明,Olig2谱系星形胶质细胞的精细突起发生了与总体跑步活动相关的可塑性变化,这表明它们积极参与运动功能。