Suppr超能文献

环状 RNA circ_0000950 通过直接海绵吸附 miR-103 促进阿尔茨海默病神经元凋亡,抑制轴突生长,升高炎症细胞因子水平。

Circular RNA circ_0000950 promotes neuron apoptosis, suppresses neurite outgrowth and elevates inflammatory cytokines levels via directly sponging miR-103 in Alzheimer's disease.

机构信息

Department of Neurology, The Fourth Affiliated Hospital of Harbin Medical University, Harbin Medical University , Harbin , China.

出版信息

Cell Cycle. 2019 Sep;18(18):2197-2214. doi: 10.1080/15384101.2019.1629773. Epub 2019 Aug 2.

Abstract

This study aimed to investigate the effect of circ_0000950/miR-103 network on regulating neuron apoptosis, neurite outgrowth and inflammation in Alzheimer's disease (AD). Cellular AD model of rat pheochromocytoma cell line PC12 cells and cellular AD model of rat cerebral cortex neurons were constructed, and the effect of circ_0000950 on apoptosis, neurite outgrowth and inflammation in both cellular AD models was determined through upregulation and knockdown of circ_0000950 expression by transfection. Compensation experiments and luciferase assay were further performed to validate the sponging effect of circ_0000950 on miR-103 as well as the mechanisms of circ_0000950/miR-103 on regulating apoptosis, neurite outgrowth and inflammation in both cellular AD models. Circ_0000950 reduced miR-103 expression and increased prostaglandin-endoperoxide synthase 2 (PTGS2) expression in both two cellular AD models. And circ_0000950 overexpression promoted neuron apoptosis, suppressed neurite outgrowth and elevated IL-1β, IL-6 and TNF-α levels compared with overexpression control, whereas circ_0000950 knockdown inhibited neuron apoptosis, enhanced neurite outgrowth and lowered IL-1β, IL-6 and TNF-α levels compared with shRNA control in both two cellular AD models. Compensation experiments along with luciferase reporter assay validated that circ_0000950 promoted cell apoptosis, suppressed neurite outgrowth and elevated inflammatory cytokines levels via directly sponging miR-103. In conclusion, circ_0000950 promotes neuron apoptosis, suppresses neurite outgrowth and elevates inflammatory cytokines levels through directly sponging miR-103 in AD.

摘要

本研究旨在探讨 circ_0000950/miR-103 网络对调节阿尔茨海默病(AD)中神经元凋亡、突起生长和炎症的影响。构建大鼠嗜铬细胞瘤 PC12 细胞 AD 细胞模型和大鼠大脑皮质神经元 AD 细胞模型,通过转染上调和下调 circ_0000950 表达,确定 circ_0000950 对两种 AD 细胞模型中细胞凋亡、突起生长和炎症的影响。进一步进行补偿实验和荧光素酶测定,以验证 circ_0000950 对 miR-103 的海绵作用以及 circ_0000950/miR-103 对两种 AD 细胞模型中细胞凋亡、突起生长和炎症的调节机制。Circ_0000950 在两种 AD 细胞模型中降低了 miR-103 的表达并增加了前列腺素内过氧化物合酶 2(PTGS2)的表达。与过表达对照相比,circ_0000950 过表达促进神经元凋亡,抑制突起生长并升高 IL-1β、IL-6 和 TNF-α水平,而与 shRNA 对照相比,circ_0000950 敲低抑制神经元凋亡,增强突起生长并降低两种 AD 细胞模型中的 IL-1β、IL-6 和 TNF-α水平。补偿实验和荧光素酶报告基因测定验证了 circ_0000950 通过直接海绵 miR-103 促进细胞凋亡,抑制突起生长并升高炎症细胞因子水平。总之,circ_0000950 通过直接海绵 miR-103 在 AD 中促进神经元凋亡,抑制突起生长并升高炎症细胞因子水平。

相似文献

引用本文的文献

1
Circular RNAs in Brain Physiology and Neurologic Diseases.大脑生理学和神经疾病中的环状RNA
Adv Exp Med Biol. 2025;1485:409-416. doi: 10.1007/978-981-96-9428-0_23.
2
Regulatory mechanism of circular RNAs in brain and neurodegenerative diseases.环状RNA在脑和神经退行性疾病中的调控机制。
Front Mol Neurosci. 2025 May 16;18:1507575. doi: 10.3389/fnmol.2025.1507575. eCollection 2025.
4

本文引用的文献

4
Circular RNA: New Regulatory Molecules.环状RNA:新型调控分子。
Bull Exp Biol Med. 2018 Apr;164(6):803-815. doi: 10.1007/s10517-018-4084-z. Epub 2018 Apr 16.
7
Circular RNA - New member of noncoding RNA with novel functions.环状RNA——具有新功能的非编码RNA新成员。
Exp Biol Med (Maywood). 2017 Jun;242(11):1136-1141. doi: 10.1177/1535370217708978. Epub 2017 May 9.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验