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脉络丛上皮细胞的条件培养基可诱导Nrf2激活的II期抗氧化反应蛋白,并抑制PC12细胞中氧化应激诱导的细胞凋亡。

Conditioned media of choroid plexus epithelial cells induces Nrf2-activated phase II antioxidant response proteins and suppresses oxidative stress-induced apoptosis in PC12 cells.

作者信息

Aliaghaei Abbas, Khodagholi Fariba, Ahmadiani Abolhassan

机构信息

NeuroBiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

J Mol Neurosci. 2014 Aug;53(4):617-25. doi: 10.1007/s12031-014-0228-4. Epub 2014 Feb 4.

Abstract

Based on the critical role of the choroid plexus (CP) in detoxification processes in the central nervous system (CNS), herein we investigated the effect of choroid plexus epithelial cells conditioned media (CPECs-CM) under oxidative conditions. CPECs were isolated from rat brains, cultured, and the conditioned media were collected. Then pheochromocytoma neuron-like cells (PC12) were treated simultaneously with CPECs-CM and H2O2 as the oxidative stressor. Next, the effect of CPECs-CM on neurite outgrowth and cell differentiation in the presence of H2O2 was determined. Our results showed that CPECs-CM improved the expansion of neurites and differentiation in PC12 cells under oxidative stress conditions. Changes in apoptotic factors, nuclear factor erythroid 2-related factor 2 (Nrf2) and γ-glutamylcysteine synthetase as the highlighted pathway in the antioxidant defense system were determined by western blot. Also, the activity of antioxidant enzymes and lipid peroxidation level were determined. CPECs-CM-treated PC12 cells could survive after exposure to H2O2 by reduction of caspase-3 cleavage and Bax level and elevation of anti-apoptotic factor Bcl2. Our data also revealed that Nrf2 activation, and consequently its downstream protein levels, increased in the presence of CPECs-CM. Based on our data, we can conclude that CPECs-CM protects PC12 cells against oxidative stress and apoptosis. It seems that CPECs secrete antioxidative agents and neurotrophic factors that have a role in the health of the CNS.

摘要

基于脉络丛(CP)在中枢神经系统(CNS)解毒过程中的关键作用,我们在此研究了氧化条件下脉络丛上皮细胞条件培养基(CPECs-CM)的作用。从大鼠脑中分离出脉络丛上皮细胞,进行培养并收集条件培养基。然后将嗜铬细胞瘤神经元样细胞(PC12)同时用CPECs-CM和作为氧化应激源的过氧化氢(H2O2)处理。接下来,确定了CPECs-CM在存在H2O2的情况下对神经突生长和细胞分化的影响。我们的结果表明,CPECs-CM在氧化应激条件下改善了PC12细胞中神经突的扩展和分化。通过蛋白质印迹法测定了凋亡因子、核因子红细胞2相关因子2(Nrf2)和γ-谷氨酰半胱氨酸合成酶(作为抗氧化防御系统中的突出途径)的变化。此外,还测定了抗氧化酶的活性和脂质过氧化水平。经CPECs-CM处理的PC12细胞在暴露于H2O2后可通过降低半胱天冬酶-3的切割和Bax水平以及提高抗凋亡因子Bcl2而存活。我们的数据还显示,在存在CPECs-CM的情况下,Nrf2激活及其下游蛋白水平增加。根据我们的数据,我们可以得出结论,CPECs-CM可保护PC12细胞免受氧化应激和凋亡。似乎CPECs分泌抗氧化剂和神经营养因子,它们对CNS的健康有作用。

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