首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Acidic oligosaccharide sugar chain, a marine-derived oligosaccharide, activates human glial cell line-derived neurotrophic factor signaling.
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Acidic oligosaccharide sugar chain, a marine-derived oligosaccharide, activates human glial cell line-derived neurotrophic factor signaling.

机译:酸性寡糖糖链(一种海洋来源的寡糖)激活人胶质细胞系来源的神经营养因子信号传导。

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Gial derived neurotrophic factor (GDNF) modulates neuronal cell differentiation during development and protects against neurodegeneration by preventing apoptosis at maturity. GDNF's role in tissue maintenance has generated interest in the therapeutic potential of GDNF in treating neurological disorders such as Parkinson's disease. Heparan sulfate has been shown to be essential for GDNF signaling and altering the levels of heparan sulfate promotes or inhibits GDNF functional activity. To search for other oligosaccharides capable of modulating GDNF activity as potential therapeutic molecules, we investigated the effect of acidic oligosaccharide sugar chain (AOSC) and its sulfated derivative on GDNF induced neurotrophic events by using Western-blotting, immunofluorescence cell staining, and immunoprecipitation techniques in PC12 cells expressing the GDNF receptors GFR alpha 1-Ret. AOSC significantly improved the neurite outgrowth and activated c-Ret phosphorylation in PC12-GFR alpha 1-Ret cells, but its sulfated derivative inhibited GDNF activity. Studies to understand the opposing biological effects of AOSC and its sulfated derivative on GDNF activity demonstrated that reduced GDNF binding to PC12-GFR alpha 1-Ret cell surface in the presence of the sulfated derivative likely suppressed GDNF activity as both AOSC and its sulfated derivatives had similar binding affinities to GDNF. This study illustrates the importance of oligosaccharide structure and charge on influencing GDNF activity and the potential use of oligosaccharides in modulating GDNF activity for therapeutic purposes.
机译:Gial衍生的神经营养因子(GDNF)在发育过程中调节神经元细胞的分化,并通过防止成熟时的凋亡来防止神经变性。 GDNF在组织维持中的作用引起了人们对GDNF在治疗神经系统疾病(如帕金森氏病)中的治疗潜力的兴趣。硫酸乙酰肝素已被证明对GDNF信号至关重要,改变硫酸乙酰肝素的水平可促进或抑制GDNF功能活性。为了寻找其他能够调节GDNF活性的寡糖作为潜在的治疗分子,我们使用Western blotting,免疫荧光细胞染色和免疫沉淀技术研究了酸性寡糖糖链(AOSC)及其硫酸化衍生物对GDNF诱导的神经营养事件的影响。 PC12细胞表达GDNF受体GFR alpha 1-Ret。 AOSC显着改善了PC12-GFR alpha 1-Ret细胞的神经突生长和激活的c-Ret磷酸化,但其硫酸化衍生物抑制了GDNF活性。旨在了解AOSC及其硫酸化衍生物对GDNF活性的相反生物学效应的研究表明,在存在硫酸化衍生物的情况下,降低GDNF与PC12-GFR alpha 1-Ret细胞表面的结合可能会抑制GDNF活性,因为AOSC及其硫酸化衍生物均具有与GDNF具有相似的结合亲和力。这项研究说明了寡糖结构和电荷对影响GDNF活性的重要性,以及寡糖在调节GDNF活性方面的潜在用途。

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