首页> 美国卫生研究院文献>The Journal of Neuroscience >Differential Regulation of Ciliary Neurotrophic Factor (CNTF) and CNTF Receptor α Expression in Astrocytes and Neurons of the Fascia Dentata after Entorhinal Cortex Lesion
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Differential Regulation of Ciliary Neurotrophic Factor (CNTF) and CNTF Receptor α Expression in Astrocytes and Neurons of the Fascia Dentata after Entorhinal Cortex Lesion

机译:内嗅皮层损伤后筋膜和星形胶质细胞神经元中睫状神经营养因子(CNTF)和CNTF受体α表达的差异调节

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摘要

Neurotrophic factors have been implicated in reactive processes occurring in response to CNS lesions. Ciliary neurotrophic factor (CNTF), in particular, has been shown to ameliorate axotomy-induced degeneration of CNS neurons and to be upregulated at wound sites in the brain. To investigate a potential role of CNTF in lesion-induced degeneration and reorganization, we have analyzed the expression of CNTF protein and CNTF receptor α (CNTFRα) mRNA in the rat dentate gyrus after unilateral entorhinal cortex lesions (ECLs), using immunocytochemistry and nonradioactive in situhybridization, respectively.In sham-operated as in normal animals, CNTF protein was not detectable by immunocytochemistry. Starting at 3 d after ECL, upregulation of CNTF expression was observed in the ipsilateral outer molecular layer (OML). Expression was maximal at around day 7, and at this stage immunoreactivity could be specifically localized to astrocytes in the ipsilateral OML. By day 14 postlesion, CNTF immunoreactivity had returned to control levels. CNTFRα mRNA was restricted to neurons of the granule cell layer in controls. Three days postlesion, prominent CNTFRα expression was observed in the deafferented OML. A similar but less prominent response was noticed in the contralateral OML. After 10 d, CNTFRα expression had returned to control levels. Double labeling for CNTFRα mRNA and glial fibrillary acidic protein (GFAP) showed that upregulation of CNTFRα occurred in reactive, GFAP-immunopositive astrocytes of the OML. A substantial reduction of CNTFRα expression in the deafferented granule cells was transiently observed at 7 and 10 d postlesion. Our results suggest a paracrine or autocrine function of CNTF in the regulation of astrocytic and neuronal responses after brain injury.
机译:神经营养因子已牵涉到响应中枢神经系统病变而发生的反应过程中。尤其是,睫状神经营养因子(CNTF)可以改善轴突切开术引起的CNS神经元变性,并在大脑伤口处被上调。为了研究CNTF在病变诱导的变性和重组中的潜在作用,我们使用免疫细胞化学和非放射性的方法分析了单侧内脏皮质损伤(ECL)后大鼠齿状回中CNTF蛋白和CNTF受体α(CNTFRα)mRNA的表达。与正常动物一样,在假手术中,CNTF蛋白无法通过免疫细胞化学检测到。从ECL后3天开始,在同侧外分子层(OML)中观察到CNTF表达的上调。表达在第7天左右达到最高,在这一阶段,免疫反应性可以特异性地定位于同侧OML中的星形胶质细胞。病变后第14天,CNTF免疫反应性已恢复至对照水平。在对照中,CNTFRαmRNA限于颗粒细胞层的神经元。患病三天后,在脱去卵的OML中观察到了显着的CNTFRα表达。在对侧OML中发现了类似但不太突出的反应。 10天后,CNTFRα表达恢复到对照水平。 CNTFRαmRNA和神经胶质原纤维酸性蛋白(GFAP)的双重标记显示,OMFR的反应性,GFAP免疫阳性星形胶质细胞发生CNTFRα的上调。在患病后7和10 d瞬时观察到脱去咖啡因的颗粒细胞中CNTFRα表达的显着降低。我们的结果表明,CNTF的旁分泌或自分泌功能可调节脑损伤后星形细胞和神经元的反应。

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