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Uncovering the Signaling Pathway behind Extracellular Guanine-Induced Activation of NO System: New Perspectives in Memory-Related Disorders

机译:揭示细胞外鸟嘌呤诱导的NO系统激活背后的信号通路:记忆相关疾病的新观点。

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Mounting evidence suggests that the guanine-based purines stand out as key player in cell metabolism and in several models of neurodegenerative disorders, such as Parkinson’s and Alzheimer’s diseases. Guanosine (GUO) and guanine (GUA) are extracellular signaling molecules derived from the breakdown of the correspondent nucleotide, GTP, and their intracellular and extracellular levels are regulated by the fine-tuned activity of two major enzymes, purine nucleoside phosphorylase (PNP) and guanine deaminase (GDA). Noteworthy, GUO and GUA, seem to play opposite roles in the modulation of cognitive functions, such as learning and memory. Indeed GUO, despite exerting neuroprotective, anti-apoptotic and neurotrophic effects, causes a decay of cognitive activities, whereas GUA administration in rats results in working memory improvement (prevented by L-NAME pre-treatment). This study was designed to investigate, in a model of SH-SY5Y neuroblastoma cell line, the signal transduction pathway activated by extracellular GUA. Altogether, our results showed that: (i) in addition to an enhanced phosphorylation of ASK1, p38 and JNK, likely linked to a non-massive and transient ROS production, the PKB/NO/sGC/cGMP/PKG/ERK cascade seems to be the main signaling pathway elicited by extracellular GUA; (ii) the activation of this pathway occurs in a pertussis-toxin sensitive manner, thus suggesting the involvement of a putative G protein coupled receptor; (iii) the GUA-induced NO production, strongly reduced by cell pre-treatment with L-NAME, is negatively modulated by the EPAC-cAMP-CaMKII pathway, which causes the over-expression of GDA that, in turn, reduces the levels of GUA. These molecular mechanisms activated by GUA may be useful to support our previous observation showing that GUA improves learning and memory functions through the stimulation of NO signaling pathway, and underscore the therapeutic potential of oral administration of guanine for treating memory-related disorders.
机译:越来越多的证据表明,基于鸟嘌呤的嘌呤在细胞代谢和多种神经退行性疾病模型(例如帕金森氏症和阿尔茨海默氏病)中起着关键作用。鸟苷(GUO)和鸟嘌呤(GUA)是源自相应核苷酸GTP分解的细胞外信号分子,其细胞内和细胞外水平受两种主要酶(嘌呤核苷磷酸化酶(PNP)和鸟嘌呤脱氨酶(GDA)。值得注意的是,GUO和GUA在调节认知功能(例如学习和记忆)中似乎起相反的作用。确实,GUO尽管发挥了神经保护,抗凋亡和神经营养作用,但会引起认知活动的衰退,而在大鼠中施用GUA则可改善工作记忆(通过L-NAME预处理可预防)。本研究旨在研究SH-SY5Y神经母细胞瘤细胞系模型中,细胞外GUA激活的信号转导途径。总的来说,我们的结果表明:(i)除了ASK1,p38和JNK的磷酸化增强(可能与非大量和短暂的ROS产生有关)外,PKB / NO / sGC / cGMP / PKG / ERK级联似乎是细胞外GUA引发的主要信号通路; (ii)该途径的激活以对百日咳毒素敏感的方式发生,因此暗示了假定的G蛋白偶联受体的参与; (iii)EPAC-cAMP-CaMKII途径对通过L-NAME进行细胞预处理而大大降低的GUA诱导的NO产生进行了EPAC-cAMP-CaMKII途径负调控,这会导致GDA的过表达,进而降低其水平GUA。 GUA激活的这些分子机制可能有助于支持我们先前的观察结果,表明GUA通过刺激NO信号传导途径改善了学习和记忆功能,并强调了口服鸟嘌呤治疗记忆相关疾病的治疗潜力。

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