首页> 美国卫生研究院文献>The Journal of Neuroscience >CNS-derived neural progenitor cells for gene transfer of nerve growth factor to the adult rat brain: complete rescue of axotomized cholinergic neurons after transplantation into the septum
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CNS-derived neural progenitor cells for gene transfer of nerve growth factor to the adult rat brain: complete rescue of axotomized cholinergic neurons after transplantation into the septum

机译:CNS衍生的神经祖细胞用于将神经生长因子基因转移至成年大鼠的大脑:移植到隔膜中后完全拯救了被轴索化的胆碱能神经元

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摘要

A CNS-derived conditionally immortalized temperature-sensitive neural progenitor (CINP) cell line was used to generate NGF-secreting cells suitable for intracerebral transplantation. The cells were transduced by repeated retroviral infection, using a vector containing the mouse NGF cDNA under the control of the LTR promoter. Subcloning at the permissive temperature (33 degrees C) identified a highly NGF-secreting clone (NGF-CINP), which contained multiple copies of the transgene and released NGF at a rate of 2 ng/hr/10(5) cells in vitro, both at 33 and 37 degrees C, which was approximately 1 order of magnitude higher than what was possible to achieve in the heterogeneously infected cell cultures. After transplantation to the brain, the NGF-CINPs differentiated into cells with a predominant glia-like morphology and migrated for a distance of 1–1.5 mm from the implantation site into the surrounding host tissue, without any signs of overgrowth and tumor formation. Grafts of NGF-CINP cells implanted into the septum of adult rats with complete fimbria-fornix lesion blocked over 90% of the cholinergic cell loss in the medial septum and grafts placed in the intact striatum induced accumulation of low-affinity NGF receptor positive fibers around the implantation site. Expression of the NGF transgene in vivo was demonstrated by RT-PCR at 2 weeks after grafting. It is concluded that the immortalized neural progenitors have a number of advantageous properties that make them highly useful experimental tools for gene transfer to the adult CNS.
机译:使用CNS衍生的条件永生化的温度敏感神经祖细胞(CINP)细胞系来生成适合脑内移植的NGF分泌细胞。使用含有在LTR启动子控制下的小鼠NGF cDNA的载体,通过反复逆转录病毒感染转导细胞。在允许的温度(33摄氏度)下进行亚克隆,可鉴定出高度分泌NGF的克隆(NGF-CINP),其中包含多个拷贝的转基因,并在体外以2 ng / hr / 10(5)的细胞速率释放NGF,在33摄氏度和37摄氏度时,温度都比在异源感染的细胞培养物中获得的温度高约1个数量级。移植到大脑后,NGF-CINPs分化为具有主要神经胶质样形态的细胞,并从植入部位迁移到周围宿主组织1-1.5 mm,没有任何过度生长和肿瘤形成的迹象。 NGF-CINP细胞移植到成年大鼠完全性纤维膜-穹ni病变的隔膜中后,阻止了内侧隔膜中90%的胆碱能细胞流失,而放置在完整纹状体中的移植物诱导了低亲和力NGF受体阳性纤维在周围的聚集植入部位。移植后2周,通过RT-PCR证实了NGF转基因在体内的表达。结论是,永生的神经祖细胞具有许多有利的特性,使其成为将基因转移到成年中枢神经系统的非常有用的实验工具。

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