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作 者:辛林伟[1] 王梨明[1] 唐际存[1] 李朝旭[1] 李强[1]
出 处:《山东医药》2014年第29期24-26,共3页Shandong Medical Journal
基 金:广西壮族自治区卫生厅计划课题基金资助(Z2011194)
摘 要:目的:观察外源性神经生长因子(NGF)对雪旺细胞(SCs)中核转录因子κB(NF-κB)mRNA表达的影响。方法体外培养SCs,用S-100免疫组化染色鉴定细胞纯度。取第4代优质细胞,随机分为实验组( NGF)、阻断组(NGF+anti-NGFR)、对照组(PBS),提取各组总mRNA,分别用紫外分光光度计、1.5%琼脂糖凝胶电泳观察结果,通过实时荧光定量PCR检测NF-κB mRNA的表达。结果体外培养的SCs与倒置显微镜下观察到的活体细胞形态一致,S-100免疫组化染色显示,SCs纯度达到91%。紫外分光光度计观察A260/A280为1.8~2.2,1.5%琼脂糖凝胶电泳可见28、18 s两条清晰条带,证实提取的mRNA质量良好。实时荧光定量PCR检测发现,与对照组、阻断组相比,实验组NF-κB mRNA的表达显著增高(P均<0.01)。结论外源性NGF可以上调SCs中NF-κB mRNA的表达。Objective To observe the influence of exogenous nerve growth factor ( NGF) on the expression of nuclear transcription factor-κB (NF-κB) mRNA of Schwann cells (SCs).Methods Schwann cells were isolated and cultured in vitro.The positive cells were counted by using S-100 immunohistochemical staining .The fourth generation of high-quality cells were randomly divided into the experimental group (NGF), blocking group (NGF+anti-NGFR) and control group (PBS).The total mRNA in each group were extracted and observed by ultraviolet spectrophotometer and 1.5%agarose gel electrophoresis , respectively , and the expression of NF-κB mRNA were detected by real-time fluorescence quantitative PCR.Results The living cell morphologies of SCs cultured in vitro were consistent with those observed under inverted microscope.S-100 immunohistochemical staining showed that the purity of SCs was 91%.Ultraviolet spectrophotometer observed that A260/A280 was 1.8-2.2, 1.5% agarose gel electrophoresis showed that there were 28 and 18 s clear bands, which confirmed the quality of extracted mRNA was good .Real time fluorescence quantitative PCR in detection of expres-sion of NF-κB mRNA showed that when compared with the control group and blocking group , the expression of NF-κB mR-NA in the experimental group was significantly increased (all P〈0.01).Conclusions Exogenous NGF can up-regulate the expression of NF-κB mRNA.
分 类 号:R741[医药卫生—神经病学与精神病学]
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