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Morphological and Phagocytic Profile of Microglia in the Developing Rat Cerebellum

机译:发育中大鼠小脑小胶质细胞的形态和吞噬特征

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摘要

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.
机译:小胶质细胞在神经发育中起着重要作用,这一点已被越来越多地认识到。小脑在出生后成熟,经历主要的生长,但是小胶质细胞在发育中的小脑中的作用尚不为人所知。使用实验室大鼠,我们使用基于设计的无偏立体学方法对整个小胶质细胞和整个发育过程中的小胶质细胞进行了定量和形态分类。我们发现,小胶质细胞形态在出生后的前3周内以区域特定的方式从变形虫变为分支状。这些形态变化伴随着产后第三周(从P17到P19)突然出现吞噬杯,与第一周相比增加了大约四倍,随后在第三周末迅速下降。在3 d窗口内,小胶质细胞吞噬杯的颗粒层(〜69%)显着高于分子层(ML;〜31%),在约67%的小胶质细胞中有较厚的突起,约33%的小胶质细胞存在。小胶质细胞与薄的过程。在ML中发现与小胶质细胞相关的吞噬杯的比例相似,具有厚或薄的过程。我们观察到一些小神经胶质吞噬杯中的细胞核碎片化和切割的caspase-3表达,可能是来自垂死的颗粒神经元。与雌性相比,在P17时,雄性小胶质细胞的过程较薄,约增加了两倍。我们的研究结果表明小胶质细胞的成熟和小胶质细胞在小脑皮层中的不均匀分布的连续过程,这暗示小胶质细胞是发展中的小脑的重要细胞成分。

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