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首页> 外文期刊>Stroke: A Journal of Cerebral Circulation >Intracerebral infusion of glial cell line-derived neurotrophic factor promotes striatal neurogenesis after stroke in adult rats.
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Intracerebral infusion of glial cell line-derived neurotrophic factor promotes striatal neurogenesis after stroke in adult rats.

机译:脑内输注胶质细胞源性神经营养因子可促进成年大鼠中风后纹状体神经发生。

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摘要

BACKGROUND AND PURPOSE: Stroke triggers increased progenitor proliferation in the subventricular zone (SVZ) and the generation of medium spiny neurons in the damaged striatum of rodents. We explored whether intrastriatal infusion of glial cell line-derived neurotrophic factor (GDNF) promotes neurogenesis after stroke. METHODS: Adult rats were subjected to 2-hour middle cerebral artery occlusion (MCAO). GDNF was infused into the ischemic striatum either during the first week after MCAO, with the animals being killed directly thereafter, or during the third and fourth weeks, with the rats being killed 1 week later. New cells were labeled with 5'-bromo-2'deoxyuridine (BrdU) on day 7 or during the second week, respectively. Neurogenesis was assessed immunocytochemically with antibodies against BrdU and neuronal, glial, or progenitor markers. GDNF receptor expression was analyzed in SVZ tissue and neurospheres by reverse transcription-polymerase chain reaction and immunocytochemistry. RESULTS: GDNF infusionincreased cell proliferation in the ipsilateral SVZ and the recruitment of new neuroblasts into the striatum after MCAO and improved survival of new mature neurons. The GDNF receptor GFRalpha1 was upregulated in the SVZ 1 week after MCAO and was coexpressed with markers of dividing progenitor cells. CONCLUSIONS: Intrastriatal infusion of GDNF in the postischemic period promotes several steps of striatal neurogenesis after stroke, partly through direct action on SVZ progenitors. Because delivery of GDNF has biological effects in the human brain, our data suggest that administration of this factor may promote neuroregenerative responses in stroke patients.
机译:背景与目的:脑卒中触发了脑室下区域(SVZ)祖细胞增殖的增加,并在啮齿动物的受损纹状体中产生了中棘神经元。我们探讨了纹状体内胶质细胞源性神经营养因子(GDNF)的输注是否促进中风后的神经发生。方法:成年大鼠接受2小时的大脑中动脉闭塞(MCAO)。在MCAO后的第一周,将GDNF注入缺血性纹状体中,然后将动物直接杀死,或在第三和第四周,将大鼠在1周后杀死。在第7天或第二周分别用5'-bromo-2'脱氧尿苷(BrdU)标记新细胞。用针对BrdU的抗体和神经元,神经胶质或祖细胞标记的免疫细胞化学方法评估神经发生。通过逆转录-聚合酶链反应和免疫细胞化学分析了SVZ组织和神经球中GDNF受体的表达。结果:MCAO后GDNF输注增加了同侧SVZ的细胞增殖,并向纹状体募集了新的成神经细胞,并提高了新的成熟神经元的存活率。 GDNF受体GFRalpha1在MCAO后1周在SVZ中上调,并与分裂祖细胞的标志物共表达。结论缺血后的纹状体内注入GDNF可促进卒中后纹状体神经发生的几个步骤,部分是通过直接作用于SVZ祖细胞。由于GDNF的传递在人脑中具有生物学作用,因此我们的数据表明,在脑卒中患者中施用该因子可能会促进神经再生反应。

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