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条件培养基可使海马神经元抵抗 kainic 酸诱导的兴奋毒性:一项体外研究

Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study.

作者信息

Bevinahal Pradeep Kumar K, Venugopal Chaitra, Yencharla Harish Chandra Prasad S, Chandanala Shashank, Trichur Raju R, Talakad Sathyaprabha N, Bhonde Ramesh R, Dhanushkodi Anandh

机构信息

School of Regenerative Medicine, Manipal University, GKVK Post, Bellary Road, Allalasandra, Near Hotel Royal Orchid, Yelahanka, Bangalore 560065, India.

Department of Neurophysiology, National Institute of Mental Health and Neurosciences, Deemed University, Hosur Road, Bangalore 560029, India.

出版信息

J Toxicol. 2014;2014:194967. doi: 10.1155/2014/194967. Epub 2014 Nov 23.

Abstract

Stem cell therapy is gaining attention as a promising treatment option for neurodegenerative diseases. The functional efficacy of grafted cells is a matter of debate and the recent consensus is that the cellular and functional recoveries might be due to "by-stander" effects of grafted cells. In the present study, we investigated the neuroprotective effect of conditioned medium (CM) derived from human embryonic kidney (HEK) cells in a kainic acid (KA) induced hippocampal degeneration model system in in vitro condition. Hippocampal cell line was exposed to KA (200 µM) for 24 hrs (lesion group) whereas, in the treatment group, hippocampal cell line was exposed to KA in combination with HEK-CM (KA + HEK-CM). We observed that KA exposure to cells resulted in significant neuronal loss. Interestingly, HEK-CM cotreatment completely attenuated the excitotoxic effects of KA. In HEK-CM cotreatment group, the cell viability was ~85-95% as opposed to 47% in KA alone group. Further investigation demonstrated that treatment with HEK-CM stimulated the endogenous cell survival factors like brain derived neurotrophic factors (BDNF) and antiapoptotic factor Bcl-2, revealing the possible mechanism of neuroprotection. Our results suggest that HEK-CM protects hippocampal neurons against excitotoxicity by stimulating the host's endogenous cell survival mechanisms.

摘要

干细胞疗法作为一种治疗神经退行性疾病的有前景的治疗选择正受到关注。移植细胞的功能疗效存在争议,最近的共识是细胞和功能的恢复可能归因于移植细胞的“旁观者”效应。在本研究中,我们在体外条件下,在 kainic 酸(KA)诱导的海马变性模型系统中研究了源自人胚肾(HEK)细胞的条件培养基(CM)的神经保护作用。海马细胞系暴露于 KA(200μM)24 小时(损伤组),而在治疗组中,海马细胞系暴露于 KA 并联合 HEK-CM(KA + HEK-CM)。我们观察到细胞暴露于 KA 导致显著的神经元损失。有趣的是,HEK-CM 联合处理完全减轻了 KA 的兴奋性毒性作用。在 HEK-CM 联合处理组中,细胞活力约为 85 - 95%,而单独 KA 处理组为 47%。进一步研究表明,用 HEK-CM 处理可刺激内源性细胞存活因子如脑源性神经营养因子(BDNF)和抗凋亡因子 Bcl-2,揭示了神经保护的可能机制。我们的结果表明,HEK-CM 通过刺激宿主的内源性细胞存活机制保护海马神经元免受兴奋性毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a422/4258312/d2d2128afd18/JT2014-194967.001.jpg

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