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一氧化氮-环磷酸鸟苷介导的甘丙肽在神经生长因子剥夺或轴突切断的感觉神经元中的表达。

NO-cGMP mediated galanin expression in NGF-deprived or axotomized sensory neurons.

作者信息

Thippeswamy Thimmasettappa, Haddley Kate, Corness Jacquie D, Howard Mark R, McKay Jennifer S, Beaucourt Stephanie M, Pope Marion D, Murphy David, Morris Richard, Hökfelt Tomas, Quinn John P

机构信息

Department of Veterinary Preclinical Science, Veterinary Faculty, University of Liverpool, Liverpool, UK.

出版信息

J Neurochem. 2007 Feb;100(3):790-801. doi: 10.1111/j.1471-4159.2006.04243.x.

Abstract

Leukaemia inhibitory factor (LIF) and nerve growth factor (NGF) are well characterized regulators of galanin expression. However, LIF knockout mice containing the rat galanin 5' proximal promoter fragment (- 2546 to + 15 bp) driving luciferase responded to axotomy in the same way as control mice. Also, LIF had no effect on reporter gene expression in vitro, neither in the presence or absence of NGF, suggesting that other factors mediate an axotomy response from the galanin promoter. We then addressed the role of nitric oxide (NO) using NGF-deprived rat dorsal root ganglion (DRG) neuron cultures infected with viral vectors containing the above-mentioned construct, and also studied endogenous galanin expression in axotomized DRG in vivo. Blocking endogenous NO in NGF-deprived DRG cultures suppressed galanin promoter activity. Consistent with this, axotomized/NGF-deprived DRG neurons expressed high levels of neuronal NO synthase (nNOS) and galanin. Further, using pharmacological NOS blockers, or adenoviral vectors expressing dominant-negative either for nNOS or soluble guanylate cyclase in vivo and in vitro, we show that the NO-cGMP pathway induces endogenous galanin in DRG neurons. We propose that both LIF and NO, acting at different promoter regions, are important for the up-regulation of galanin, and for DRG neuron survival and regeneration after axotomy.

摘要

白血病抑制因子(LIF)和神经生长因子(NGF)是已得到充分表征的甘丙肽表达调节因子。然而,携带驱动荧光素酶的大鼠甘丙肽5'近端启动子片段(-2546至+15 bp)的LIF基因敲除小鼠对轴突切断的反应与对照小鼠相同。此外,无论有无NGF,LIF在体外对报告基因表达均无影响,这表明其他因子介导了甘丙肽启动子的轴突切断反应。然后,我们利用感染了含有上述构建体的病毒载体的NGF剥夺大鼠背根神经节(DRG)神经元培养物研究了一氧化氮(NO)的作用,并在体内研究了轴突切断的DRG中内源性甘丙肽的表达。在NGF剥夺的DRG培养物中阻断内源性NO可抑制甘丙肽启动子活性。与此一致的是,轴突切断/NGF剥夺的DRG神经元表达高水平的神经元型一氧化氮合酶(nNOS)和甘丙肽。此外,使用药理学一氧化氮合酶阻滞剂或在体内和体外表达nNOS或可溶性鸟苷酸环化酶显性阴性的腺病毒载体,我们表明NO-cGMP途径可诱导DRG神经元中的内源性甘丙肽。我们提出,LIF和NO作用于不同的启动子区域,对甘丙肽的上调以及轴突切断后DRG神经元的存活和再生都很重要。

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