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TrkA与p75(NTR)之间的功能协同作用通过ERK1/2和AP-1活性增加GAP-43和p21(CIP/WAF)基因的转录,从而加速神经元分化。

Functional cooperation between TrkA and p75(NTR) accelerates neuronal differentiation by increased transcription of GAP-43 and p21(CIP/WAF) genes via ERK1/2 and AP-1 activities.

作者信息

Diolaiti Daniel, Bernardoni Roberto, Trazzi Stefania, Papa Antonella, Porro Antonio, Bono Françoise, Herbert Jean-Marc, Perini Giovanni, Della Valle Giuliano

机构信息

Department of Biology, University of Bologna, Via Selmi 3, 40126 Bologna, Italy.

出版信息

Exp Cell Res. 2007 Aug 15;313(14):2980-92. doi: 10.1016/j.yexcr.2007.06.002. Epub 2007 Jun 19.

Abstract

The biological complexity of NGF action is achieved by binding two distinct neurotrophin receptors, TrkA and p75(NTR). While several reports have provided lines of evidence on the interaction between TrkA and p75(NTR) at the plasma membrane, much fewer data are available on the consequence of such an interaction in terms of intracellular signaling. In this study, we have focused on how p75(NTR) may affect TrkA downstream signaling with respect to neuronal differentiation. Here, we have shown that cooperation between p75(NTR) and TrkA results in an increased NGF-mediated TrkA autophosphorylation, leads to a sustained activation of ERK1/2 and accelerates neurite outgrowth. Interestingly, neurite outgrowth is concomitant with a selective enhancement of the AP-1 activity and the transcriptional activation of genes such as GAP-43 and p21(CIP/WAF), known to be involved in the differentiation process. Collectively, our results unveil a functional link between the specific expression profile of neurotrophin receptors in neuronal cells and the NGF-mediated regulation of the differentiation process possibly through a persistent ERKs activation and the selective control of the AP-1 activity.

摘要

NGF作用的生物学复杂性是通过与两种不同的神经营养因子受体TrkA和p75(NTR)结合来实现的。虽然有几份报告提供了关于TrkA和p75(NTR)在质膜上相互作用的证据,但关于这种相互作用在细胞内信号传导方面的后果的数据却少得多。在本研究中,我们重点关注p75(NTR)如何在神经元分化方面影响TrkA下游信号传导。在此,我们表明p75(NTR)与TrkA之间的协同作用导致NGF介导的TrkA自磷酸化增加,导致ERK1/2的持续激活并加速神经突生长。有趣的是,神经突生长伴随着AP-1活性的选择性增强以及已知参与分化过程的基因如GAP-43和p21(CIP/WAF)的转录激活。总的来说,我们的结果揭示了神经元细胞中神经营养因子受体的特定表达谱与NGF介导的分化过程调节之间的功能联系,这可能是通过持续的ERK激活和对AP-1活性的选择性控制来实现的。

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