NRG1β-overexpressing mesenchymal stem cell-derived exosomes alleviate oxygen-glucose deprivation-mediated neuronal injury via the miR-296-3p/MAOA axis.

IF 4.4 3区 医学 Q2 NEUROSCIENCES
Frontiers in Cellular Neuroscience Pub Date : 2026-07-27 eCollection Date: 2026-01-01 DOI:10.3389/fncel.2026.1809758
Kuihua Wang, Haizhen Xu, Xiaohui Ji, Shengjie Zhu, YanJun Lin, Hua Chen, Xiangping Chen, Xuyang Jiang, He Zhou, Jianxin Ye, Xiaoping Cui
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引用次数: 0

Abstract

Background: Cerebral ischemic injury is a severe neurological disorder necessitating effective therapeutic strategies. Neuregulin-1β (NRG1β) and microRNAs are critical for neuroprotection, but the mechanisms by which NRG1β regulates microRNAs in neuronal injury are not fully understood.

Methods: We characterized mesenchymal stem cells (MSCs) through their phenotypic markers and multilineage differentiation potential, confirming NRG1β overexpression in engineered MSCs. Transmission electron microscopy and nanoparticle tracking analysis were used to isolate and characterize exosomes. In vitro studies evaluated the effects of MSC/NRG1β-exosomes on OGD-treated HT-22 neuronal cells.

Results: Mesenchymal stem cells/NRG1β-exosomes significantly enhanced HT-22 neuronal survival while reducing apoptosis and reactive oxygen species (ROS). The treatment reduced oxidative stress by lowering malondialdehyde (MDA) levels and boosting superoxide dismutase (SOD) activity. It also inhibited inflammatory cytokines such as IL-1β, TNF-α, and IL-6. Studies conducted in vivo with a middle cerebral artery occlusion model demonstrated that MSC/NRG1β-exosomes led to a reduction in infarct size, enhanced histopathological results 24 h after injury. Mechanistically, these exosomes were enriched with miR-296-3p, targeting monoamine oxidase A (MAOA) for downregulation. Inhibition of miR-296-3p or MAOA overexpression negated the protective effects of MSC/NRG1β-exosomes.

Conclusion: Our findings demonstrate that exosomes derived from NRG1β-overexpressing mesenchymal stem cells (MSCs) exert neuroprotective effects against ischemic injury by upregulating miR-296-3p. This microRNA targets MAOA, leading to a reduction in apoptosis, oxidative stress, and inflammation. These results highlight the therapeutic potential of MSC/NRG1β-exosomes and the miR-296-3p/MAOA signaling axis in the treatment of ischemic brain injury.

过表达nrg1 β-的间充质干细胞衍生外泌体通过miR-296-3p/MAOA轴减轻氧-葡萄糖剥夺介导的神经元损伤。
背景:脑缺血损伤是一种严重的神经系统疾病,需要有效的治疗策略。神经调节蛋白-1β (NRG1β)和microrna对神经保护至关重要,但NRG1β在神经元损伤中调控microrna的机制尚不完全清楚。方法:我们通过表型标记和多系分化潜能对间充质干细胞(MSCs)进行了表征,证实了NRG1β在工程MSCs中的过表达。利用透射电子显微镜和纳米颗粒跟踪分析分离和表征外泌体。体外研究评估了MSC/ nrg1 β-外泌体对ogd处理的HT-22神经元细胞的影响。结果:间充质干细胞/ nrg1 β-外泌体显著提高HT-22神经元的存活率,同时减少细胞凋亡和活性氧(ROS)。该处理通过降低丙二醛(MDA)水平和提高超氧化物歧化酶(SOD)活性来减少氧化应激。它还能抑制炎症细胞因子,如IL-1β、TNF-α和IL-6。在大脑中动脉闭塞模型中进行的体内研究表明,MSC/ nrg1 β-外泌体导致梗死面积减少,损伤后24小时的组织病理学结果增强。在机制上,这些外泌体富含miR-296-3p,靶向单胺氧化酶A (MAOA)下调。抑制miR-296-3p或MAOA过表达否定了MSC/ nrg1 β-外泌体的保护作用。结论:我们的研究结果表明,来自nrg1 β-过表达的间充质干细胞(MSCs)的外泌体通过上调miR-296-3p对缺血性损伤具有神经保护作用。这种microRNA靶向MAOA,导致细胞凋亡、氧化应激和炎症的减少。这些结果突出了MSC/ nrg1 β-外泌体和miR-296-3p/MAOA信号轴在缺血性脑损伤治疗中的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.90
自引率
3.80%
发文量
627
审稿时长
6-12 weeks
期刊介绍: Frontiers in Cellular Neuroscience is a leading journal in its field, publishing rigorously peer-reviewed research that advances our understanding of the cellular mechanisms underlying cell function in the nervous system across all species. Specialty Chief Editors Egidio D‘Angelo at the University of Pavia and Christian Hansel at the University of Chicago are supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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