Gugliandolo Agnese, Chiricosta Luigi, Calì Gabriella, Rollin Patrick, Perenzoni Daniele, Iori Renato, Mazzon Emanuela, D'Angiolini Simone
IRCCS Centro Neurolesi "Bonino-Pulejo", Via Provinciale Palermo, Contrada Casazza, 98124 Messina, Italy.
Institute of Organic and Analytical Chemistry (ICOA), Université d'Orléans, UMR 7311, BP 6759, F-45067 Orléans, France.
Int J Mol Sci. 2025 Aug 24;26(17):8220. doi: 10.3390/ijms26178220.
α-Cyclodextrin/Moringin (α-CD/MOR) is an isothiocyanate showing neuroprotective and antioxidant properties. In this work, we studied in differentiated NSC-34 motor neurons cell line the molecular pathways activated following a treatment of 96 h with α-CD/MOR at different doses, namely 0.5, 5 and 10 μM. Taking advantage of comparative transcriptomic analysis, we retrieved the differentially expressed genes (DEGs) and we mapped DEGs to synaptic genes using the SynGO database. Then, we focused on the biological pathways in which they are involved. We observed that the prolonged treatment with α-CD/MOR significantly modulated biological processes and cellular components associated with synaptic organization. Interestingly, the KEGG pathway "Regulation of actin cytoskeleton" was overrepresented, alongside pathways related to synapses and axon guidance. Specifically, SPIA analysis indicated that the "Regulation of actin cytoskeleton" pathway was found to be activated with the highest dose of α-CD/MOR. Moreover, α-CD/MOR also modulated transcription factors involved in synaptic plasticity, such as . These results could indicate that α-CD/MOR can influence synaptic functions and organization, being involved in synaptic plasticity through the modulation of actin dynamics.
α-环糊精/辣木素(α-CD/MOR)是一种具有神经保护和抗氧化特性的异硫氰酸酯。在这项研究中,我们在分化的NSC-34运动神经元细胞系中研究了用不同剂量(即0.5、5和10μM)的α-CD/MOR处理96小时后激活的分子途径。利用比较转录组分析,我们检索了差异表达基因(DEG),并使用SynGO数据库将DEG映射到突触基因。然后,我们关注它们所涉及的生物学途径。我们观察到,用α-CD/MOR进行长时间处理可显著调节与突触组织相关的生物学过程和细胞成分。有趣的是,KEGG途径“肌动蛋白细胞骨架的调节”以及与突触和轴突导向相关的途径都高度富集。具体而言,SPIA分析表明,“肌动蛋白细胞骨架的调节”途径在最高剂量的α-CD/MOR处理下被激活。此外,α-CD/MOR还调节参与突触可塑性的转录因子,如 。这些结果可能表明,α-CD/MOR可以影响突触功能和组织,通过调节肌动蛋白动力学参与突触可塑性。