首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Neuroprotective effects of estrogen against beta-amyloid toxicity are mediated by estrogen receptors in cultured neuronal cells.
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Neuroprotective effects of estrogen against beta-amyloid toxicity are mediated by estrogen receptors in cultured neuronal cells.

机译:雌激素对β-淀粉样蛋白毒性的神经保护作用是由培养的神经元细胞中的雌激素受体介导的。

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摘要

Although estrogen is known to exert beneficial effects on Alzheimer's disease, its underlying cellular mechanisms have not been clear. In this study we investigated whether or not neuroprotective effects of estrogen are mediated by estrogen receptors (ERs). Treatment of estrogen (1.8 nM) reduced beta-amyloid (Abeta)-induced death of ER-expressing W4 cells. This effect of estrogen was blocked by a specific ER blocker ICI 182,780. When estrogen was treated to HT22 cells, which lack functional ERs, Abeta-induced cell death was not affected. Transfection of HT22 cells with human ERalpha, but not ERbeta, restored protective action of estrogen against Abeta. Hoechst staining revealed that estrogen protected ERalpha-expressing cells by blocking Abeta-induced apoptosis. These results indicate that estrogen blocks Abeta-induced cell death via ERalpha-dependent pathways.
机译:尽管已知雌激素可对阿尔茨海默氏病发挥有益作用,但其潜在的细胞机制尚不清楚。在这项研究中,我们调查了雌激素的神经保护作用是否由雌激素受体(ER)介导。雌激素(1.8 nM)的治疗减少了β-淀粉样蛋白(Abeta)诱导的表达ER的W4细胞死亡。特定的ER阻滞剂ICI 182,780阻断了雌激素的这种作用。当雌激素治疗缺乏功能性ER的HT22细胞时,Abeta诱导的细胞死亡不会受到影响。用人ERalpha(而不是ERbeta)转染HT22细胞,恢复了雌激素对Abeta的保护作用。 Hoechst染色显示,雌激素可通过阻断Abeta诱导的细胞凋亡来保护表达ERalpha的细胞。这些结果表明,雌激素可通过ERalpha依赖性途径阻断Abeta诱导的细胞死亡。

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