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Cross-talk between growth factor and purinergic signalling regulates Schwann cell proliferation

机译:生长因子与嘌呤能信号传导之间的串扰调节施万细胞增殖

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Axons provide multiple mitogenic signals to Schwann cells (SCs), yet at an appropriate stage of development, SCs stop dividing despite the mitogenic action ofaxo-lemma and growth factors. This implies that the effect of mitogens on cell proliferation may be context-dependent, having different effects on cell proliferation depending upon other signals in the extracellular environment. Recent research has shown that the effects of adenosine on SC proliferation depend upon the growth factor environment, and that the extracellular signal-regulated kinase/mitogen-activated protein kinase (ERK/ MAPK) signalling pathway is an important point of integration between purinergic and growth factor signalling. In the absence of growth factors, adenosine is mitogenic and associated with stimulation of the ERK/MAPK pathway in SCs. However, in the presence of growth factors (platelet-derived growth factor or neuregulin), adenosine has the opposite effect, inhibiting proliferation and ERK/MAPK activation. Together these findings suggest a mechanism by which increased neural impulse activity could modulate growth factor signalling to both positively and negatively regulate SC proliferation before the onset of myelination.
机译:轴突为Schwann细胞(SCS)提供多种丝分裂性信号,但在适当的显影阶段,SCS停止除去XO XO-LEMMA和生长因子。这意味着可以对细胞增殖的效果对细胞增殖的影响可能是依赖性的,这对细胞增殖的不同作用取决于细胞外环境中的其他信号。最近的研究表明,腺苷对SC增殖的影响取决于生长因子环境,并且细胞外信号调节激酶/丝裂性蛋白激酶(ERK / MAPK)信号通路是嘌呤能和生长之间的重要积分因子信令。在没有生长因子的情况下,腺苷是丝分裂性的,并且与SCS中ERK / MAPK途径的刺激相关。然而,在存在生长因子(血小板衍生的生长因子或Neuregulin)中,腺苷具有相反的效果,抑制增殖和ERK / MAPK活化。这些研究结果表明了一种机制,增加了神经脉冲活性的机制可以在髓鞘开始发作之前对阳性和负调节SC增殖调节生长因子信号传导。

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