circSPG21 protects against intervertebral disc disease by targeting miR-1197/ATP1B3

合成代谢 核心 机制(生物学) 环状RNA 核糖核酸 基因沉默 癌症研究 生物信息学 基因表达 细胞 生物 计算生物学 椎间盘 基因 细胞生物学 解剖 遗传学 生物化学 哲学 认识论
作者
Yizhen Huang,Zhenlei Zhang,Jianle Wang,Shuying Shen,Yuanwen Teng,Yining Xu,Zizheng Chen,Bin Fang,Jianjun Ma
出处
期刊:Experimental and Molecular Medicine [Springer Nature]
卷期号:53 (10): 1547-1558 被引量:13
标识
DOI:10.1038/s12276-021-00674-z
摘要

The abnormal expression of circular RNAs (circRNAs) is associated with numerous human diseases. This study investigated the mechanism by which circRNA acts as competitive endogenous RNA in the regulation of degenerative intervertebral disc disease (IVDD). Decreased expression of circSPG21 was detected in degenerated nucleus pulposus cells (NPCs), the function of circSPG21 in NPCs was explored and verified, and the downstream target of circSPG21 was investigated. The interaction between circSPG21 and miR-1197 and its target gene (ATP1B3) was studied by online database prediction and molecular biological verification. Finally, the circSPG21/miR-1197/ATP1B3 axis was verified in the mouse tail-looping model. The expression of circSPG21 in the nucleus pulposus in IVDD was directly related to an imbalance of anabolic and catabolic factors, which affected cell senescence. circSPG21 was found to play a role in human NPCs by acting as a sponge of miR-1197 and thereby affecting ATP1B3. The regulation of circSPG21 provides a potentially effective therapeutic strategy for IVDD.

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