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MDMA 是否可以通过 mGlu5 代谢型谷氨酸受体促进小鼠胚胎干细胞的干性特征?

Could MDMA Promote Stemness Characteristics in Mouse Embryonic Stem Cells via mGlu5 Metabotropic Glutamate Receptors?

机构信息

1. Department of Cell and Molecular Biology, Cell Science Research Center, Royan Institute for Animal Biotechnology, ACECR, Isfahan, Iran ; 2. Isfahan Neurosciences research center, Isfahan University of Medical Sciences, Isfahan, Iran ; 3. Islamic Azad University, Najafabad Branch, Isfahan, Iran.

出版信息

Cell J. 2012 Fall;14(3):185-92. Epub 2012 Dec 12.

Abstract

OBJECTIVE

Ecstasy, or 3, 4 (±) methylenedioxymethamphetamine (MDMA), is a potent neurotoxic drug. One of the mechanisms for its toxicity is the secondary release of glutamate. Mouse embryonic stem cells (mESCs) express only one glutamate receptor, the metabotropic glutamate receptor 5 (mGlu5), which is involved in the maintenance and self-renewal of mESCs. This study aims to investigate whether MDMA could influence self-renewal via the mGlu5 receptor in mESCs.

MATERIALS AND METHODS

In this expremental study, we used immunocytochemistry and reverse transcription-polymerase chain reaction (RT-PCR) to determine the presence of the mGlu5 receptor in mESCs. The expression of mGlu5 was evaluated after MDMA was added to mESCs throughout neural precursor cell formation as group 1 and during neural precursor cell differentiation as group 2. The stemness characteristic in treated mESCs by immunofluorescence and flow cytometry was studied. Finally, caspase activity was evaluated by fluorescence staining in the treated group. One-way ANOVA or repeated measure of ANOVA according to the experimental design was used for statistical analyses.

RESULTS

In this study mGlu5 expression was shown in mESCs. In terms of neuronal differentiation, MDMA affected mGlu5 expression during neural precursor cell formation (group 1) and not during neural precursor differentiation (group 2). MDMA (450 µM) induced a significant increment in self-renewal properties in mESCs but did not reverse 2-methyl-6(phenylethynyl) pyridine (MPEP, 1 µM), a non-competitive selective mGlu5 antagonist. Fluorescence staining with anti-caspase 3 showed a significant increase in the number of apoptotic cells in the MDMA group.

CONCLUSION

WE OBSERVED A DUAL ROLE FOR MDMA ON MESCS: reduced proliferation and maintenance of self-renewal. The lack of decreasing stemness characteristic in presence of MPEP suggests that MDMA mediates its role through a different mechanism that requires further investigation. In conclusion, despite being toxic, MDMA maintains stemness characteristics.

摘要

目的

摇头丸,或 3,4(±)亚甲二氧基甲基苯丙胺(MDMA)是一种强效神经毒性药物。其毒性的一种机制是谷氨酸的二次释放。小鼠胚胎干细胞(mESCs)仅表达一种谷氨酸受体,即代谢型谷氨酸受体 5(mGlu5),该受体参与 mESCs 的维持和自我更新。本研究旨在探讨 MDMA 是否可以通过 mESCs 中的 mGlu5 受体影响自我更新。

材料和方法

在这项实验研究中,我们使用免疫细胞化学和逆转录聚合酶链反应(RT-PCR)来确定 mESCs 中 mGlu5 受体的存在。将 MDMA 添加到 mESCs 中以形成神经前体细胞(第 1 组)和分化为神经前体细胞(第 2 组)时,评估 mGlu5 的表达。通过免疫荧光和流式细胞术研究处理后的 mESCs 的干性特征。最后,通过荧光染色评估处理组中的半胱天冬酶活性。根据实验设计,使用单因素方差分析或重复测量方差分析进行统计学分析。

结果

本研究显示 mGlu5 在 mESCs 中表达。就神经元分化而言,MDMA 影响神经前体细胞形成过程中的 mGlu5 表达(第 1 组),而不影响神经前体细胞分化(第 2 组)。MDMA(450μM)诱导 mESCs 自我更新特性显著增加,但不能逆转非竞争性选择性 mGlu5 拮抗剂 2-甲基-6(苯乙炔基)吡啶(MPEP,1μM)。用抗半胱天冬酶 3 荧光染色显示 MDMA 组凋亡细胞数量显著增加。

结论

我们观察到 MDMA 对 mESCs 有双重作用:减少增殖和维持自我更新。在存在 MPEP 的情况下,干性特征没有减少,这表明 MDMA 通过需要进一步研究的不同机制发挥其作用。总之,尽管 MDMA 具有毒性,但它能维持干细胞的特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfec/3584439/0bdad136c884/Cell-J-14-185-g01.jpg

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