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寻找调节突触可塑性的去极化诱导基因以及介导神经元分化的神经营养因子诱导基因。

Searching for depolarization-induced genes that modulate synaptic plasticity and neurotrophin-induced genes that mediate neuronal differentiation.

作者信息

Herschman H R, Ferguson G D, Feldman J D, Farias-Eisner R, Vician L

机构信息

Department of Biological Chemistry, UCLA, Los Angeles, CA 90095, USA.

出版信息

Neurochem Res. 2000 May;25(5):591-602. doi: 10.1023/a:1007546600535.

Abstract

We identify and characterize two classes of immediate-early genes: (i) genes, induced by depolarization in neurons, that play a role in depolarization-induced neuronal plasticity and (ii) genes, induced in neuronal precursors by neurotrophins, that play a causal role in neurotrophin-directed neuronal differentiation. We use rat PC12 pheochromocytoma cells to identify (i) genes preferentially induced by [depolarization or forskolin] versus [Nerve Growth Factor (NGF) or Epidermal Growth Factor (EGF)] and (ii) genes preferentially induced by NGF versus EGF. We describe (i) a collection of genes preferentially induced by depolarization/forskolin in PC12 cells and by kainic acid in vivo, and (ii) a collection of genes preferentially induced by NGF. The synaptotagmin IV gene encodes a synaptic vesicle protein whose level is modulated by depolarization. NGF preferentially induces the urokinase-plasminogen activator receptor in PC12 cells. Antisense oligonucleotide and anti-UPAR antibody experiments demonstrate that NGF-induced UPAR expression is required for NGF-driven PC12 cell differentiation.

摘要

我们鉴定并表征了两类即早基因

(i)由神经元去极化诱导的基因,其在去极化诱导的神经元可塑性中发挥作用;(ii)由神经营养因子在神经元前体细胞中诱导的基因,其在神经营养因子导向的神经元分化中起因果作用。我们使用大鼠嗜铬细胞瘤PC12细胞来鉴定(i)相对于[神经生长因子(NGF)或表皮生长因子(EGF)]优先由[去极化或福斯高林]诱导的基因,以及(ii)相对于EGF优先由NGF诱导的基因。我们描述了(i)在PC12细胞中优先由去极化/福斯高林以及在体内由海藻酸诱导的一组基因,以及(ii)优先由NGF诱导的一组基因。突触结合蛋白IV基因编码一种突触小泡蛋白,其水平受去极化调节。NGF在PC12细胞中优先诱导尿激酶型纤溶酶原激活物受体。反义寡核苷酸和抗UPAR抗体实验表明,NGF驱动的PC12细胞分化需要NGF诱导的UPAR表达。

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