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嵌合抗原受体 T 细胞通过上调脑源性神经营养因子的合成和分泌来减轻脑缺血再灌注引起的内质网应激反应。

CART attenuates endoplasmic reticulum stress response induced by cerebral ischemia and reperfusion through upregulating BDNF synthesis and secretion.

机构信息

Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing, People's Republic of China.

出版信息

Biochem Biophys Res Commun. 2013 Jul 12;436(4):655-9. doi: 10.1016/j.bbrc.2013.05.142. Epub 2013 Jun 14.

Abstract

Cocaine and amphetamine regulated transcript (CART), a neuropeptide, has shown strong neuroprotective effects against cerebral ischemia and reperfusion (I/R) injury in vivo and in vitro. Here, we report a new effect of CART on ER stress which is induced by cerebral I/R in a rat model of middle cerebral artery occlusion (MCAO) or by oxygen and glucose deprivation (OGD) in cultured cortical neurons, as well as a new functionality of BDNF in the neuroprotection by CART against the ER stress in cerebral I/R. The results showed that CART was effective in reducing the neuronal apoptosis and expression of ER stress markers (GRP78, CHOP and cleaved caspase12), and increasing the BDNF expression in I/R injury rat cortex both in vivo and in vitro. In addition, the effects of CART on ischemia-induced neuronal apoptosis and ER stress were suppressed by tyrosine receptor kinase B (TrkB) IgG, whereas the effects of CART on BDNF transcription, synthesis and secretion were abolished by CREB siRNA. This work suggests that CART is functional in inhibiting the cerebral I/R-induced ER stress and neuronal apoptosis by facilitating the transcription, synthesis and secretion of BDNF in a CREB-dependent way.

摘要

可卡因和苯丙胺调节转录物 (CART) 是一种神经肽,已显示出对体内和体外脑缺血再灌注 (I/R) 损伤具有很强的神经保护作用。在这里,我们报告了 CART 对脑 I/R 诱导的培养皮质神经元中 ER 应激的新作用,以及 CART 对脑 I/R 中 ER 应激的神经保护作用中 BDNF 的新功能。结果表明,CART 可有效减少神经元凋亡和 ER 应激标志物 (GRP78、CHOP 和 cleaved caspase12) 的表达,并增加 I/R 损伤大鼠皮质中的 BDNF 表达,无论是在体内还是体外。此外,CART 对缺血诱导的神经元凋亡和 ER 应激的作用被酪氨酸受体激酶 B (TrkB) IgG 抑制,而 CART 对 BDNF 转录、合成和分泌的作用被 CREB siRNA 消除。这项工作表明,CART 通过 CREB 依赖性方式促进 BDNF 的转录、合成和分泌,从而在功能上抑制脑 I/R 诱导的 ER 应激和神经元凋亡。

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