首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Neuregulin 1 up-regulates the expression of nicotinic acetylcholine receptors through the ErbB2/ErbB3-PI3K-MAPK signaling cascade in adult autonomic ganglion neurons
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Neuregulin 1 up-regulates the expression of nicotinic acetylcholine receptors through the ErbB2/ErbB3-PI3K-MAPK signaling cascade in adult autonomic ganglion neurons

机译:神经调节蛋白1通过ErbB2 / ErbB3-PI3K-MAPK信号传导级联在成人自主神经节神经元中上调烟碱型乙酰胆碱受体的表达

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摘要

We investigated effects of Neuregulin 1 (NRG1) on the expression of nicotinic acetylcholine receptor (nAChR) in major pelvic ganglion (MPG) from adult rat. MPG neurons were found to express transcripts for type I and III NRG1s as well as α and β-type epidermal growth factor (EGF)-like domains. Of the four ErbB receptor isoforms, ErbB1, ErbB2, and ErbB3 were expressed in MPG neurons. Treating MPG with NRG1β significantly increased the transcript and protein level of the nAChR α3 and β4 subunits. Consistent with these molecular data, nicotinic currents (IACh) were significantly up-regulated in NRG1β-treated sympathetic and parasympathetic MPG neurons. In contrast, the type III NRG1 and the α form of the NRG1 failed to alter the IACh. Inhibition of the ErbB2 tyrosine kinase completely abolished the effects of NRG1β on the IACh. Stimulation of the ErbB receptors by NRG1β activated the phosphatidylinositol-3-kinase (PI3K) and mitogen-activated protein kinase (MAPK). Immunoblot analysis revealed that PI3K-mediated activation of Akt preceded Erk1/2 activation in NRG1β-treated MPG neurons. Furthermore, specific PI3K inhibitors abrogated the phosphorylation of Erk1/2, while inhibition of MEK did not prevent the phosphorylation of Akt. Taken together, these findings suggest that NRG1 up-regulates nAChR expression via the ErbB2/ErbB3-PI3K-MAPK signaling cascade and may be involved in maintaining the ACh-mediated synaptic transmission in adult autonomic ganglia.
机译:我们调查了成年大鼠主要骨盆神经节(MPG)中神经调节蛋白1(NRG1)对烟碱型乙酰胆碱受体(nAChR)表达的影响。发现MPG神经元表达I型和III型NRG1以及α和β型表皮生长因子(EGF)样结构域的转录本。在四种ErbB受体同工型中,ErbB1,ErbB2和ErbB3在MPG神经元中表达。用NRG1β处理MPG可显着提高nAChRα3和β4亚基的转录本和蛋白质水平。与这些分子数据一致,NRG1β治疗的交感神经和副交感神经MPG神经元的烟碱电流(IACh)明显上调。相反,III型NRG1和NRG1的α形式未能改变IACh。 ErbB2酪氨酸激酶的抑制作用完全消除了NRG1β对IACh的作用。 NRG1β刺激ErbB受体激活了磷脂酰肌醇3-激酶(PI3K)和丝裂原激活的蛋白激酶(MAPK)。免疫印迹分析显示,在NRG1β处理的MPG神经元中,PI3K介导的Akt激活先于Erk1 / 2激活。此外,特定的PI3K抑制剂废除了Erk1 / 2的磷酸化,而MEK的抑制则不能阻止Akt的磷酸化。综上所述,这些发现表明NRG1通过ErbB2 / ErbB3-PI3K-MAPK信号级联反应上调nAChR表达,并可能参与维持成人自主神经节中ACh介导的突触传递。

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