成年大鼠局灶性脑缺血后室管膜/室下区细胞向梗死周围区迁移并分化为神经元和星形胶质细胞。

Peng-bo Zhang, Yong Liu, Jie Li, Qian-yan Kang, Ying-fang Tian, Xin-lin Chen, Jian-jun Zhao, Qin-dong Shi, Tu-sheng Song, Yi-hua Qian
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引用次数: 0

摘要

目的:观察大鼠局灶性脑缺血后室管膜/室下区细胞的迁移和分化,揭示梗死周围区新生神经细胞的来源。方法:选用体重250 ~ 350 g的正常成年雄性大鼠。在大脑中动脉闭塞(MCAO)前,侧脑室注射10 μ l 0.2% DiI预标记室管膜/室下带细胞。缺血后采用累积BrdU标记检测新生细胞,双免疫荧光染色检测细胞分化情况。用激光共聚焦显微镜观察标记的细胞。结果:在非缺血对照大鼠中,dii标记的细胞位于室管膜/室下区。局灶性脑缺血后,胼胝体、邻近纹状体和皮层可见DiI-标记细胞,MCAO后第14天纹状体或皮层梗死周围区可见DiI/BrdU/胶质纤维酸性蛋白(GFAP)阳性细胞或DiI/BrdU/神经元核抗原(NeuN)阳性细胞。结论:局灶性脑缺血后,室管膜/室下区细胞迁移至梗死周围区,并分化为神经元和星形胶质细胞。这一发现可能对了解成体神经干细胞的来源以及通过增强脑损伤后内源性神经发生来开发新的治疗干预策略具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ependymal/subventricular zone cells migrate to the peri-infarct region and differentiate into neurons and astrocytes after focal cerebral ischemia in adult rats.

Objective: To investigate the migration and differentiation of ependymal/subventricular zone cells after focal cerebral ischemia in rats, and reveal the origin of the newly generated neural cells in the peri-infarct region.

Methods: Normal adult male Sprague Dawley rats weighing 250-350 g were used in this study. Before middle cerebral artery occlusion (MCAO), 10 microl of 0.2% DiI was injected into the lateral ventricle for prelabeling the ependymal/subventricular zone cells. After ischemia, cumulative BrdU labeling was employed to detect the newly generated cells and double immunofluorescent staining to identify cell differentiation. The labeled cells were observed with laser confocal microscopy.

Results: In the non-ischemic control rats, DiI-labeled cells resided in the ependyma/subventricular zone. After focal cerebral ischemia, DiI-labeled cells were found in the corpus callosum, adjacent striatum and cortex, and some DiI/BrdU/glial fibrillary acidic protein (GFAP)-positive cells or DiI/BrdU/ neuronal nuclear antigen (NeuN)-positive cells were observed in the peri-infarct region in the striatum or cortex since day 14 after MCAO.

Conclusion: After focal cerebral ischemia, ependymal/subventricular zone cells migrate into the peri-infarct region where they differentiate into neurons and astrocytes. This finding may be important for understanding the source of adult neural stem cells and for developing new therapeutic intervention strategy through enhancing endogenous neurogenesis after brain injury.

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