首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >The synergistic effects of NGF and IGF-1 on neurite growth in adult sensory neurons: convergence on the PI 3-kinase signaling pathway.
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The synergistic effects of NGF and IGF-1 on neurite growth in adult sensory neurons: convergence on the PI 3-kinase signaling pathway.

机译:NGF和IGF-1对成人感觉神经元神经突生长的协同作用:在PI 3激酶信号通路上的收敛。

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摘要

Nerve growth factor (NGF) and insulin-like growth factor-1 (IGF-1) play an important role in promoting axonal growth from dorsal root ganglion (DRG) neurons. Adult DRG neurons exhibit neurotrophin-independent survival, providing an excellent system with which to study trophic factor effects on neurite growth in the absence of significant survival effects. Using young adult rat DRG neurons we have demonstrated a synergistic effect of NGF plus IGF (N + I), compared with either factor alone, in promoting neurite growth. Not only does the presence of NGF and IGF-1 enhance neurite initiation, it also significantly augments the extent of neurite branching and elongation. We have also examined potential mechanism(s) underlying this synergistic effect. Immunoblotting experiments of classical growth factor intermediary signalling pathways (PI 3-K-Akt-GSK-3 and Ras-Raf-MAPK) were performed using phospho-specific antibodies to assess activation state. We found that activation of Akt and MAPK correlated with neurite elongation and branching. However, using pharmacological inhibitors, we observed that a PI 3-K pathway involving both Akt and GSK-3 appeared to be more important for neurite extension and branching than MAPK-dependent signalling. In fact, inhibition of activation of MAPK with U0126 resulted in increased neuritic branching, possibly as a result of the concomitant increase observed in phospho-Akt. Furthermore, inhibition of GSK3 (which is negatively regulated by phosphorylation on S9/S21) also resulted in increased growth. Our data point to signalling convergence upon the PI 3-K-Akt-GSK-3 pathway that underlies the NGF plus IGF synergism. In addition, to our knowledge, this is the first report in primary neurons that inhibition of GSK3 results in an enhanced neurite growth.
机译:神经生长因子(NGF)和胰岛素样生长因子1(IGF-1)在促进背根神经节(DRG)神经元的轴突生长中起重要作用。成年DRG神经元表现出不依赖于神经营养蛋白的存活,提供了一个出色的系统来研究营养因子对神经突生长的影响,而没有明显的存活作用。使用成年大鼠DRG神经元,我们证明了与单独使用任一因子相比,NGF和IGF(N + I)在促进神经突生长方面具有协同作用。 NGF和IGF-1的存在不仅增强了神经突的起始,而且还显着增加了神经突分支和伸长的程度。我们还研究了这种协同作用的潜在机制。经典的生长因子中间信号通路(PI 3-K-Akt-GSK-3和Ras-Raf-MAPK)的免疫印迹实验使用磷酸特异性抗体进行评估,以评估其激活状态。我们发现Akt和MAPK的激活与神经突伸长和分支相关。但是,使用药理学抑制剂,我们观察到涉及Akt和GSK-3的PI 3-K途径对于神经突延伸和分支似乎比MAPK依赖性信号传导更为重要。实际上,用U0126抑制MAPK激活会导致神经分支增加,这可能是由于磷酸化Akt伴随增加。此外,对GSK3的抑制(通过S9 / S21的磷酸化负调控)也导致生长增加。我们的数据指向在NGF加IGF协同作用基础上的PI 3-K-Akt-GSK-3途径上发出信号收敛。另外,据我们所知,这是原代神经元中第一个报道,抑制GSK3会导致神经突生长增强。

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