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The influence of tumour necrosis factor- ?± (TNF-?±) on amyloid-?2 (A?2)-degrading enzymes in vitro

机译:肿瘤坏死因子-α±(TNF-α±)对淀粉样β2(Aβ2)降解酶的影响

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Pro-inflammatory cytokines, such as tumour necrosis factor-α (TNF-α), are increased in serum and CSF in Alzheimer's disease (AD). We investigated the effect of TNF-α on gene and protein expression levels of Aβ degrading enzymes (ACE, ECE-1, ECE- 2, IDE and NEP) in vitro. Differentiated (DC) and non-differentiated (NDC) neuroblastoma cells (SH-SY5Y) were exposed to TNF-α for 15 minutes and 3 hours and protein and gene expression levels measured using western blotting or sandwich ELISA (ECE-2), and real time-PCR (RT-PCR). Only ECE-2 protein levels decreased significantly in NDCs in a dose-dependent manner after 15 minutes of TNF-α exposure but reverted to basal levels after 3 hours. Basal NEP gene expression levels were higher in control DCs compared to NDCs but TNF-α treatment did not significantly alter the levels of expression of any of the Aβ degrading enzymes. In conclusion, apart from a transient reduction in ECE-2 protein levels, TNF-α had no impact in our in vitro experimental system on transcription or translation of any of our selected mediators of Aβ degradation.
机译:阿尔茨海默氏病(AD)的血清和CSF中促炎性细胞因子(例如肿瘤坏死因子-α(TNF-α))增加。我们研究了TNF-α对Aβ降解酶(ACE,ECE-1,ECE-2,IDE和NEP)的基因和蛋白质表达水平的影响。将分化的(DC)和未分化的(NDC)神经母细胞瘤细胞(SH-SY5Y)暴露于TNF-α15分钟和3小时,并使用Western印迹或夹心ELISA(ECE-2)测量蛋白质和基因表达水平,并实时PCR(RT-PCR)。在TNF-α暴露15分钟后,仅NCE中的ECE-2蛋白水平以剂量依赖性方式显着降低,但在3小时后恢复为基础水平。与NDC相比,对照DC的基础NEP基因表达水平更高,但TNF-α处理并未显着改变任何Aβ降解酶的表达水平。总之,除了ECE-2蛋白水平短暂降低外,TNF-α在我们的体外实验系统中对我们选择的Aβ降解介体的转录或翻译没有影响。

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