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雌激素受体 α 对人神经母细胞瘤细胞凋亡相关基因的差异调控。

Differential regulation of apoptosis-associated genes by estrogen receptor alpha in human neuroblastoma cells.

机构信息

Institute for Pathobiochemistry, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.

出版信息

Restor Neurol Neurosci. 2013;31(2):199-211. doi: 10.3233/RNN-120272.

Abstract

PURPOSE

The neuroendocrinology of female sex hormones is of great interest for a variety of neuropsychiatric disorders. In fact, estrogens and estrogen receptors (ERs) exert neuromodulatory and neuroprotective functions. Here we investigated potential targets of the ER subtype alpha that may mediate neuroprotection and focused on direct modulators and downstream executors of apoptosis.

METHODS

We employed subclones of human neuroblastoma cells (SK-N-MC) stably transfected with one of the ER subtypes, ERalpha or ERbeta. Differences between the cell lines regarding the mRNA expression levels were examined by qPCR, changes on protein levels were examined by Western Blot and immunocytochemistry. Differences concerning apoptosis induction were analysed by cell survival assays which included primary rat neurons.

RESULTS

In this report we show a potent protection against apoptosis-stimuli in ERalpha expressing cells compared to controls lacking ERalpha. In fact, almost a complete silencing of Caspase 3 expression in SK-ERalpha cells compared to SK-01 control transfected cells was observed. In addition, prosurvival bcl2, bag1 and bag3 expression was highly up-regulated in the presence of ERalpha.

CONCLUSION

Taken together, we identified Caspase 3, BAG1 and BAG3 as key targets of ERalpha in neuronal cells that may play a role in ERalpha-mediated neuroprotection.

摘要

目的

女性性激素的神经内分泌学对于多种神经精神疾病具有重要意义。事实上,雌激素和雌激素受体(ER)发挥神经调节和神经保护作用。在这里,我们研究了 ER 亚型α可能介导神经保护的潜在靶标,并集中研究了凋亡的直接调节剂和下游执行者。

方法

我们使用稳定转染了 ER 亚型之一(ERalpha 或 ERbeta)的人神经母细胞瘤细胞(SK-N-MC)亚克隆。通过 qPCR 检查细胞系之间 mRNA 表达水平的差异,通过 Western Blot 和免疫细胞化学检查蛋白水平的变化。通过包括原代大鼠神经元在内的细胞存活测定分析凋亡诱导的差异。

结果

在本报告中,我们显示 ERalpha 表达细胞对凋亡刺激具有强大的保护作用,与缺乏 ERalpha 的对照细胞相比。事实上,与 SK-01 对照转染细胞相比,SK-ERalpha 细胞中 Caspase 3 的表达几乎完全沉默。此外,在存在 ERalpha 的情况下,bcl2、bag1 和 bag3 的生存促进表达被高度上调。

结论

总之,我们确定 Caspase 3、BAG1 和 BAG3 是 ERalpha 在神经元细胞中的关键靶标,它们可能在 ERalpha 介导的神经保护中发挥作用。

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