Disruption of the GluA2/GAPDH complex using TAT-GluA2NT1-3-2 peptide protects against AMPAR-mediated excitotoxicity after epilepsy

Disruption of the GluA2/GAPDH complex using TAT-GluA2NT1-3-2 peptide protects against AMPAR-mediated excitotoxicity after epilepsy
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使用 TAT-GluA2NT1-3-2 肽破坏 GluA2/GAPDH 复合物可防止癫痫后 AMPAR 介导的兴奋性毒性

DOI:
10.1097/wnr.0000000000000996
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发表时间:
2018-03
期刊:
影响因子:
1.7
通讯作者:
王纪文
王纪文
中科院分区:
医学4区
文献类型:
--
作者:
张晶卉;王纪文

文献摘要

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癫痫后的兴奋性毒性和神经元死亡涉及-氨基-3-羟基-5-甲基-4-异恶唑丙酸受体(AMPARs)。它与甘油醛-3-磷酸脱氢酶(GAPDH)形成蛋白质复合物,并在激活后共同内化
Excitotoxicity and neuronal death following epilepsy involve -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs). It forms a protein complex with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and co-internalizes upon activation