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胚胎发育期小鼠大脑皮层中小胶质细胞的复杂入侵模式。

Complex invasion pattern of the cerebral cortex bymicroglial cells during development of the mouse embryo.

机构信息

Hasselt University, BIOMED, Agoralaan (Gebouw C), Diepenbeek B-3590, Belgium.

出版信息

Glia. 2013 Feb;61(2):150-63. doi: 10.1002/glia.22421. Epub 2012 Sep 21.

Abstract

Microglia are the immune cells of the central nervous system. They are suspected to play important roles in adult synaptogenesis and in the development of the neuronal network. Microglial cells originate from progenitors in the yolk sac. Although it was suggested that they invade the cortex at early developmental stages in the embryo, their invasion pattern remains largely unknown. To address this issue we analyzed the pattern of cortical invasion by microglial cells in mouse embryos at the onset of neuronal cell migration using in vivo immunohistochemistry and ex vivo time-lapse analysis of microglial cells. Microglial cells begin to invade the cortex at 11.5 days of embryonic age (E11.5). They first accumulate at the pial surface and within the lateral ventricles, after which they spread throughout the cortical wall, avoiding the cortical plate region in later embryonic ages. The invasion of the cortical parenchyma occurs in different phases. First, there is a gradual increase of microglial cells between E10.5 and E14.5. From E14.5 to E15.5 there is a rapid phase with a massive increase in microglia, followed by a slow phase again from E15.5 until E17.5. At early stages, many peripheral microglia are actively proliferating before entering the parenchyma. Remarkably, activated microglia accumulate in the choroid plexus primordium, where they are in the proximity of dying cells. Time-lapse analysis shows that embryonic microglia are highly dynamic cells.

摘要

小胶质细胞是中枢神经系统的免疫细胞。它们被怀疑在成年突触发生和神经元网络发育中发挥重要作用。小胶质细胞起源于卵黄囊中的祖细胞。尽管有人提出它们在胚胎早期发育阶段侵入皮质,但它们的侵入模式在很大程度上仍然未知。为了解决这个问题,我们使用体内免疫组织化学和体外小胶质细胞延时分析,分析了神经元细胞迁移开始时小鼠胚胎中小胶质细胞侵入皮质的模式。小胶质细胞在胚胎 11.5 天时(E11.5)开始侵入皮质。它们首先聚集在软脑膜表面和侧脑室内部,然后在以后的胚胎时期扩散到整个皮质壁,避开皮质板区域。皮质实质的侵入发生在不同的阶段。首先,从 E10.5 到 E14.5,小胶质细胞逐渐增加。从 E14.5 到 E15.5,有一个快速阶段,小胶质细胞大量增加,然后从 E15.5 到 E17.5 再次进入缓慢阶段。在早期阶段,许多外周小胶质细胞在进入实质之前积极增殖。值得注意的是,激活的小胶质细胞在脉络丛原基中积聚,在那里它们靠近死亡的细胞。延时分析表明,胚胎小胶质细胞是高度动态的细胞。

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