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[海马神经元癫痫样放电后ERK1/2级联反应与c-fos表达的相关性研究]

[Correlative research between ERK1/2 cascade and c-fos expression after hippocampal neuron epileptiform discharge].

作者信息

Xu Zu-Cai, Liu Hua, Chen Yang-Mei

机构信息

Department of Neurology, Second Affiliated Hospital, Chongqing Medical University, Chongqing 400010, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2008 Jun 17;88(23):1639-42.

Abstract

OBJECTIVE

To investigate the correlation between ERK1/2 cascade and c-fos after hippocampal neuron epileptiform discharge.

METHODS

Hippocampal neurons were collected from Wistar rats and cultured in magnesium-free extra-cellular fluid to establish hippocampal neuron epileptiform discharge model. Then the hippocampal neurons were divided into 2 groups: inhibitor group, added with 10 micromol/L U0126, inhibitor of ERK 1/2 pathway, and control group without any treatment, got at 0 min). Using double-label immunofluorescence, laser scanning confocal microscopy was performed to detect the disposition of phosphorylated-ERK1/2(p-ERK1/2) and c-fos in the neurons. Western blotting was used to detect the expression of p-ERK1/2 and c-fos 0 min, 30 min, 2 h, 6 h, 12 h, and 24 h following corresponding treatment

RESULTS

Double-label immunofluorescence examination displayed that there was p-ERK1/2 in both the cytoplasm and nucleus, but c-fos in the nucleus only. Western blotting manifested that p-ERK1/2 was observed at each time points in the model group, and the expression pattern of c-fos was the same as p-ERK1/2, which peaked 30 min after treatment. In the inhibitor group, p-ERK1/2 was inhibited completely, and c-fos was decreased obviously. The c-fos expression levels at different time points of the inhibitor group were all significantly lower than those of the model group (all P < 0.01).

CONCLUSION

After hippocampal neuron epileptiform discharge, ERK1/2 is activated for a long time, and the expression of c-fos is downregulated by blocking the phosphorylation of ERK1/2.

摘要

目的

探讨海马神经元癫痫样放电后细胞外调节蛋白激酶1/2(ERK1/2)信号转导通路与原癌基因c-fos之间的相关性。

方法

取Wistar大鼠海马神经元,在无镁细胞外液中培养以建立海马神经元癫痫样放电模型。将海马神经元分为2组:抑制剂组,加入10 μmol/L ERK1/2通路抑制剂U0126;对照组,不做任何处理。在0分钟时取材。采用双标免疫荧光法,运用激光扫描共聚焦显微镜检测神经元中磷酸化ERK1/2(p-ERK1/2)和c-fos的定位。采用蛋白质免疫印迹法检测相应处理后0分钟、30分钟、2小时、6小时、12小时和24小时p-ERK1/2和c-fos的表达。

结果

双标免疫荧光检测显示,p-ERK1/2在细胞质和细胞核中均有表达,而c-fos仅在细胞核中表达。蛋白质免疫印迹法显示,模型组各时间点均能检测到p-ERK1/2,c-fos的表达模式与p-ERK1/2相同,在处理后30分钟达到峰值。抑制剂组中,p-ERK1/2被完全抑制,c-fos明显降低。抑制剂组不同时间点的c-fos表达水平均显著低于模型组(均P < 0.01)。

结论

海马神经元癫痫样放电后,ERK1/2被长时间激活,阻断ERK1/2磷酸化可下调c-fos的表达。

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