神经保护
亨廷顿蛋白
神经退行性变
氧化应激
亨廷顿病
KEAP1型
细胞生物学
活性氧
生物
程序性细胞死亡
转录因子
药理学
化学
生物化学
突变体
内科学
医学
细胞凋亡
疾病
基因
作者
Siew Chin Chan,Chih‐Wei Tung,Chia-Wei Lin,Yun-Shiuan Tung,Po-Min Wu,Pei‐Hsun Cheng,Chuan‐Mu Chen,Shang‐Hsun Yang
标识
DOI:10.1016/j.freeradbiomed.2023.10.407
摘要
Huntington's disease (HD) is a devastating neurodegenerative disorder characterized by the accumulation of mutant Huntingtin protein (mHTT) and oxidative stress-induced neuronal damage. Based on previous reports, microRNA-196a (miR-196a) has emerged as a potential therapeutic target due to its neuroprotective effects in various neurodegenerative diseases. However, whether miR-196a functions through antioxidative effects is still unknown. In this study, we demonstrated that HD models, both in vitro and in vivo, exhibit elevated levels of reactive oxygen species (ROS) and increased neuronal death, and miR-196a mitigates ROS levels and reduces cell death in HD cells. Moreover, we elucidated that miR-196a facilitates the translocation of nuclear factor erythroid 2 (Nrf2) into the nucleus, enhancing the transcription of antioxidant genes, including heme oxygenase-1 (HO-1). We further identified ubiquitin-specific peptidase 15 (USP15), a direct target of miR-196a related to the Nrf2 pathway, and USP15 exacerbates mHTT aggregate formation while partially counteracting miR-196a-induced reductions in mHTT levels. Taken together, these findings shed light on the multifaceted role of miR-196a in HD, highlighting its potential as a therapeutic avenue for ameliorating oxidative stress and neurodegeneration in this debilitating disease.
科研通智能强力驱动
Strongly Powered by AbleSci AI