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CRE-mediated gene expression in cerebral ischemia

机译:CRE介导的脑缺血中的基因表达

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Although accumulating evidence indicates that cAMP response element binding protein (CREB) phosphorylation is upregulated after cerebral ischemia, it remains uncertain whether CREB phosphorylation induced after ischemia leads to CRE-mediated gene transcription and is involved in cell survival or not. Using CRE-LacZ transgenic mice, we demonstrated that CRE-mediated gene expression was found in a subset of pCREB-positive neurons after transient global and focal cerebral ischemia and in cultured neurons after exposure to glutamate. Treatment with CRE-decoy oligonucleotide suppressed upregulation of BCL-2 expression and accelerated neuronal damage after exposure to glutamate. CRE-mediated gene expression occurs in neurons after metabolic stresses and exerts its neuroprotective action through production of survival-promoting molecules such as anti-apoptotic protein BCL-2.
机译:尽管累积证据表明,在脑缺血后,营养响应元件结合蛋白(CREB)磷酸化在脑缺血后上调,但缺血后诱导的CREB磷酸化仍然不确定,仍然不确定CRE介导的基因转录并参与细胞存活。使用CRE-Lacz转基因小鼠,我们证明了在暴露于谷氨酸后的瞬时全球和局灶性脑缺血和培养的神经元后,在PCReB阳性神经元的子集中发现Cre-介导的基因表达。用Cre-cooy寡核苷酸治疗抑制了Bcl-2表达的上调和暴露于谷氨酸后的加速神经元损伤。 CRE介导的基因表达发生在代谢应力之后神经元中,通过生产促进抗凋亡蛋白Bcl-2等生存分子来施加其神经保护作用。

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