首页> 美国卫生研究院文献>Iranian Journal of Veterinary Research >High neuronal/astroglial differentiation plasticity of adult rat hippocampal neural stem/progenitor cells in response to the effects of embryonic and adult cerebrospinal fluids
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High neuronal/astroglial differentiation plasticity of adult rat hippocampal neural stem/progenitor cells in response to the effects of embryonic and adult cerebrospinal fluids

机译:成年大鼠海马神经干/祖细胞的高神经元/星形胶质细胞分化可塑性响应胚胎和成年脑脊髓液的作用

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摘要

Hippocampal neural stem/progenitor cells (hipp-NS/PCs) of the adult mammalian brain are important sources of neuronal and gial cell production. In this study, the main goal is to investigate the plasticity of these cells in neuronal/astroglial differentiations. To this end, the differentiation of the hipp-NS/PCs isolated from 3-month-old Wistar rats was investigated in response to the embryonic cerebrospinal fluid (E-CSF) including E13.5, E17-CSF and the adult cerebrospinal fluid (A-CSF), all extracted from rats. CSF samples were selected based on their effects on cell behavioral parameters. Primary cell culture was performed in the presence of either normal or high levels of KCL in a culture medium. High levels of KCL cause cell depolarization, and thus the activation of quiescent NSCs. Results from immunocytochemistry (ICC) and semi-quantitative RT-PCR (sRT-PCR) techniques showed that in E-CSF-treated groups, neuronal differentiation increased (E17>E13.5). In contrast, A-CSF decreased and increased neuronal and astroglial differentiations, respectively. Cell survivability and/or proliferation (S/P), evaluated by an MTT assay, increased by E13.5 CSF, but decreased by both E17 CSF and A-CSF. Based on the results, it is finally concluded that adult rat hippocampal proliferative cells are not restricted progenitors but rather show high plasticity in neuronal/astroglial differentiation according to the effects of CSF samples. In addition, using high concentrations of KCL in the primary cell culture led to an increase in the number of NSCs, which in turn resulted in the increase in neuronal or astroglial differentiations after CSF treatment.
机译:成年哺乳动物脑的海马神经干/祖细胞(hipp-NS / PCs)是神经元和神经胶质细胞产生的重要来源。在这项研究中,主要目的是研究这些细胞在神经元/星形胶质细胞分化中的可塑性。为此,研究了从3个月大的Wistar大鼠中分离出的hipp-NS / PCs对胚胎脑脊液(E-CSF)的反应,其中包括E13.5,E17-CSF和成年脑脊液( A-CSF),均从大鼠中提取。根据CSF对细胞行为参数的影响选择样本。在培养基中正常或高水平的KCL存在下进行原代细胞培养。高水平的KCL会引起细胞去极化,从而激活静态NSC。免疫细胞化学(ICC)和半定量RT-PCR(sRT-PCR)技术的结果表明,在E-CSF治疗组中,神经元分化增加(E17> E13.5)。相反,A-CSF分别减少和增加神经元和星形胶质细胞的分化。通过MTT分析评估的细胞存活率和/或增殖(S / P),由E13.5 CSF增加,但由E17 CSF和A-CSF降低。根据结果​​,最后得出结论,根据CSF样品的作用,成年大鼠海马增殖细胞不是限制性祖细胞,而是在神经元/星形胶质细胞分化中显示出高可塑性。此外,在原代细胞培养物中使用高浓度的KCL会导致NSC数量增加,进而导致CSF治疗后神经元或星形胶质细胞分化的增加。

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