Ito Umeo, Nagasao Jun, Kawakami Emiko, Oyanagi Kiyomitsu
Department of Neuropathology, Tokyo Metropolitan Institute for Neuroscience, Musashidai, Fuchu-shi, Tokyo, Japan.
Stroke. 2007 Sep;38(9):2577-83. doi: 10.1161/STROKEAHA.107.484394. Epub 2007 Aug 2.
Because the mechanism for scavenging acidophilic electron-dense dead neurons disseminated among the neuritic networks of surviving neurons in the ischemic penumbra of the cerebral cortex is still obscure, we investigated the fate of them up to 24 weeks after the ischemic insult.
Stroke-positive animals were selected according to their stroke index score during the first 10-minute left carotid occlusion done twice with a 5-hour interval. The animals were killed at various times after the second ischemic insult. Ultrathin sections including the second through fourth cortical layers were obtained from the neocortex coronally sectioned at the infundibular level in which the penumbra appeared and was observed by electron microscopy. We determined the percentages of resting, activated, and phagocytic microglia and astrocytes in the specimens obtained at various times postischemia.
The electron-dense neurons had been fragmented into granular pieces by invading astrocytic processes from the periphery of the dead neurons and only the central portion remained. These granular pieces were dispersed along the extracellular spaces in the neuropil. By 8 to 24 weeks, the central core portion became a tiny vesicular particle (3.5 to 5.5 mum in diameter) with a central dot. Microglia and astrocytes phagocytized these dispersed granular pieces.
We found a novel scavenger mechanism in the ischemic penumbra, one by which dead neurons were fragmented by invading small astrocytic processes and only a thinned-out core portion remained, which finally became a tiny vesicular particle. The dispersed fragmented pieces were phagocytized by the microglia and astrocytes late, at 8 to 24 weeks postischemia.
由于在大脑皮质缺血半暗带中,清除散布于存活神经元神经突网络中的嗜酸性电子致密死亡神经元的机制仍不清楚,我们研究了缺血损伤后长达24周这些神经元的转归。
根据首次10分钟左侧颈动脉闭塞(间隔5小时进行两次)期间的卒中指数评分选择卒中阳性动物。在第二次缺血损伤后的不同时间处死动物。从在视交叉水平冠状切片的新皮质获取包括第二至第四皮质层的超薄切片,该水平出现半暗带并通过电子显微镜观察。我们确定了缺血后不同时间获得的标本中静息、活化和吞噬性小胶质细胞及星形胶质细胞的百分比。
电子致密神经元已被从死亡神经元周边侵入的星形胶质细胞突起分割成颗粒状碎片,仅中央部分残留。这些颗粒状碎片沿神经毡中的细胞外间隙分散。到8至24周时,中央核心部分变成直径为3.5至5.5μm的微小囊泡状颗粒,带有一个中心点。小胶质细胞和星形胶质细胞吞噬这些分散的颗粒状碎片。
我们在缺血半暗带中发现了一种新的清除机制,即死亡神经元被侵入的小星形胶质细胞突起分割,仅残留一个变薄的核心部分,最终变成一个微小的囊泡状颗粒。分散的碎片在缺血后8至24周被小胶质细胞和星形胶质细胞晚期吞噬。