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首页> 外文期刊>Acta Pharmacologica Sinica >Antiapoptotic effect both in vivo and in vitro of A20 gene when transfected into rat hippocampal neurons
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Antiapoptotic effect both in vivo and in vitro of A20 gene when transfected into rat hippocampal neurons

机译:A20基因转染大鼠海马神经元后的体内外抗凋亡作用

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Aim: To evaluate the antiapoptotic effect of the A20 gene in primary hippocampal neurons both in vivo and in vitro. Methods: Primary hippocampal neurons in embryonic day 18 (E18) rats were transfected with the A20 gene by using the new Nucleofector electroporation transfection method. We then examined, whether A20 -neurons possessed anti-apoptotic abilities after TNF-α stimulation in vitro. A20-neurons and pcDNA3 -neurons were transplanted into the penumbra of the brains of rats that had been subjected to 90-min of ischemia induced by left middle cerebral artery occlusion (MCAO). Results: A20-neurons resisted TNF-α induced apoptosis in vitro. The apoptosis rate of neurons overexpressing A20 (28.46%+-3.87%) was lower than that in neurons transfected with pcDNA3 (53.06%+-5.36%). More A20-neurons survived in the penumbra both 3-d and 7-d after transplantation than did sham pcDNA3 neurons. Conclusion: The novel function of A20 may make it a potential targets for the gene therapy for neurological diseases.
机译:目的:评价A20基因在体内和体外对原代海马神经元的抗凋亡作用。方法:采用新的Nucleofector电穿孔转染方法,将胚胎第18天(E18)大鼠原代海马神经元转染A20基因。然后,我们检查了TNF-α体外刺激后,A20-神经元是否具有抗凋亡能力。将A20-神经元和pcDNA3-神经元移植到已经遭受左大脑中动脉闭塞(MCAO)诱导的缺血90分钟的大鼠大脑半影中。结果:A20神经元在体外抵抗TNF-α诱导的细胞凋亡。过量表达A20的神经元的凋亡率(28.46%+-3.87%)低于转染pcDNA3的神经元的凋亡率(53.06%+-5.36%)。与假pcDNA3神经元相比,移植后3 d和7 d在半影中存活的A20神经元更多。结论:A20的新功能可能使其成为神经疾病基因治疗的潜在靶标。

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