Department of Pharmacology, University of Maryland School of Medicine , Baltimore, Maryland 21201.
Department of Pharmacology, University of Maryland School of Medicine , Baltimore, Maryland 21201 ; Program in Neuroscience, University of Maryland School of Medicine , Baltimore, Maryland 21201.
eNeuro. 2015 Aug 31;2(4). doi: 10.1523/ENEURO.0036-15.2015. eCollection 2015 Jul-Aug.
Microglia are being increasingly recognized as playing important roles in neurodevelopment. The cerebellum matures postnatally, undergoing major growth, but the role of microglia in the developing cerebellum is not well understood. Using the laboratory rat we quantified and morphologically categorized microglia throughout the vermis and across development using a design-based unbiased stereology method. We found that microglial morphology changed from amoeboid to ramified during the first 3 postnatal weeks in a region specific manner. These morphological changes were accompanied by the sudden appearance of phagocytic cups during the third postnatal week from P17 to P19, with an approximately fourfold increase compared with the first week, followed by a prompt decline at the end of the third week. The microglial phagocytic cups were significantly higher in the granular layer (∼69%) than in the molecular layer (ML; ∼31%) during a 3 d window, and present on ∼67% of microglia with thick processes and ∼33% of microglia with thin processes. Similar proportions of phagocytic cups associated to microglia with either thick or thin processes were found in the ML. We observed cell nuclei fragmentation and cleaved caspase-3 expression within some microglial phagocytic cups, presumably from dying granule neurons. At P17 males showed an approximately twofold increase in microglia with thin processes compared with females. Our findings indicate a continuous process of microglial maturation and a nonuniform distribution of microglia in the cerebellar cortex that implicates microglia as an important cellular component of the developing cerebellum.
小胶质细胞在神经发育中扮演着越来越重要的角色,这一点正逐渐得到人们的认可。小脑在出生后仍在继续发育,体积显著增大,但小胶质细胞在发育中小脑内的作用尚未得到充分理解。本研究采用基于设计的无偏体视学方法,使用实验室大鼠作为研究对象,对整个小脑蚓部和整个发育过程中小胶质细胞进行了定量和形态分类。我们发现,在出生后的前 3 周内,小胶质细胞的形态从阿米巴样向有突分支样转变,这种形态变化具有区域特异性。这种形态变化伴随着吞噬杯的突然出现,出现在第 17 天至第 19 天的第 3 个出生后周,与第 1 周相比增加了约 4 倍,然后在第 3 周结束时迅速下降。在 3 天的窗口内,与分子层(ML)相比,颗粒层(GL)中的小胶质细胞吞噬杯(∼69%)显著更高,而 ML 中的小胶质细胞吞噬杯(∼31%)则显著较低。在具有厚突起的小胶质细胞(∼67%)和具有薄突起的小胶质细胞(∼33%)上都存在着类似比例的吞噬杯。在 ML 中,与具有厚或薄突起的小胶质细胞相关的吞噬杯比例相似。我们观察到一些小胶质细胞吞噬杯内的细胞核碎片化和 cleaved caspase-3 表达,推测是来自死亡的颗粒神经元。在 P17 时,雄性大鼠中具有薄突起的小胶质细胞比例比雌性大鼠高约 2 倍。我们的研究结果表明,小胶质细胞成熟是一个连续的过程,小脑皮质中小胶质细胞的分布不均匀,这表明小胶质细胞是发育中小脑的重要细胞成分。