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GITR 的细胞内部分通过反向调节 Erk 和 NF-κB 信号通路增强 NGF 促进的轴突生长。

The intracellular portion of GITR enhances NGF-promoted neurite growth through an inverse modulation of Erk and NF-κB signalling.

机构信息

Department of Anatomy and Neuroscience, Biosciences Institute, University College Cork , Cork , Ireland.

出版信息

Biol Open. 2012 Oct 15;1(10):1016-23. doi: 10.1242/bio.20121024. Epub 2012 Aug 20.

Abstract

NF-κB transcription factors play a key role in regulating the growth of neural processes in the developing PNS. Although several secreted proteins have been shown to activate NF-κB to inhibit the growth of developing sympathetic neurons, it is unknown how the endogenous level of NF-κB activity present in these neurons is restricted to allow neurite growth to occur during their normal development. Here we show that activation of the glucocorticoid-induced tumour necrosis factor receptor (GITR) inhibits NF-κB activation while promoting the activation of Erk in developing sympathetic neurons. Conversely, inhibition of GITR results in an increase in NF-κB dependent gene transcription and a decrease in Erk activation leading to a reduction in neurite growth. These findings show that GITR signalling can regulate the extent of sympathetic neurite growth through an inverse modulation of Erk and NF-κB signalling, which provides an optimal environment for NGF-promoted growth.

摘要

NF-κB 转录因子在调节周围神经系统发育过程中神经突起的生长中起着关键作用。虽然已经证明几种分泌蛋白可以激活 NF-κB 来抑制交感神经元的生长,但尚不清楚这些神经元中存在的内源性 NF-κB 活性水平是如何受到限制的,以允许神经突起在正常发育过程中生长。在这里,我们表明,糖皮质激素诱导的肿瘤坏死因子受体 (GITR) 的激活抑制 NF-κB 的激活,同时促进发育中的交感神经元中 Erk 的激活。相反,GITR 的抑制导致 NF-κB 依赖性基因转录增加和 Erk 激活减少,从而导致神经突起生长减少。这些发现表明,GITR 信号可以通过反向调节 Erk 和 NF-κB 信号来调节交感神经突起生长的程度,这为 NGF 促进的生长提供了最佳环境。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b2/3507174/afa44e9280f1/bio-01-10-1016-f01.jpg

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