Astrocyte-derived Exosomal GJA1-20 k Targets Pink1-mediated Mitophagy to Attenuate Traumatic Brain Injury.

IF 4.3 2区 医学 Q1 CLINICAL NEUROLOGY
Yalun Li, Wei Chen, Jiugeng Feng
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引用次数: 0

Abstract

Connexin 43 (Cx43), particularly its truncated isoform GJA1-20 k, has shown promise in mitigating neuronal injury through mitochondrial regulation. This study aimed to investigate the therapeutic potential of astrocyte-derived extracellular vesicles (EVs) enriched with GJA1-20 k (Exo-GJA1-20 k) for treating traumatic brain injury (TBI). Primary astrocytes were isolated and transfected with an adeno-associated viral vector to overexpress GJA1-20 k. EVs were extracted and characterized using nanoparticle tracking analysis and Western blotting. A controlled cortical impact (CCI) model of TBI was established in mice, followed by daily administration of Exo-GJA1-20 k via tail vein injections. Mitochondrial function, neuroinflammation, pyroptosis, and cognitive outcomes were evaluated through molecular assays, histological staining, and behavioral tests, including the Morris Water Maze and open field tests. Exo-GJA1-20 k treatment significantly improved mitochondrial quality control by enhancing mitophagy and reducing mitochondrial dysfunction. Pyroptosis, driven by the NLRP3 inflammasome, was notably suppressed, with significant reductions in NLRP3, ASC, and IL-1β expression levels. Behavioral analyses revealed enhanced cognitive performance, as evidenced by shorter escape latencies in the Morris Water Maze and reduced anxiety-like behaviors in the open field test in Exo-GJA1-20 k-treated mice compared to controls. Importantly, the therapeutic effects of Exo-GJA1-20 k were diminished in Pink1-knockout mice, underscoring the dependence on Pink1-mediated mitophagy. This study demonstrates that Exo-GJA1-20 k exerts neuroprotective effects by modulating the mitophagy-NLRP3 inflammasome axis, alleviating neuroinflammation, and mitigating cognitive deficits in a TBI model. These findings propose a novel therapeutic strategy for addressing TBI-induced neuronal damage and underscore the potential of EV-based therapies for treating neurological disorders.

星形胶质细胞来源的外泌体gja1 - 20k靶向pink1介导的线粒体自噬以减轻创伤性脑损伤。
连接蛋白43 (Cx43),特别是其截短的异构体gja1 - 20k,已显示出通过线粒体调节减轻神经元损伤的希望。本研究旨在探讨富含gja1 - 20k (exo - gja1 - 20k)的星形胶质细胞来源的细胞外囊泡(ev)对创伤性脑损伤(TBI)的治疗潜力。分离原代星形胶质细胞,用腺相关病毒载体转染过表达gja1 - 20k的星形胶质细胞。利用纳米颗粒跟踪分析和Western blotting对ev进行提取和表征。建立小鼠脑外伤控制性皮质冲击(CCI)模型,每日尾静脉注射exo - gja1 - 20k。线粒体功能、神经炎症、焦亡和认知结果通过分子分析、组织学染色和行为测试(包括Morris水迷宫和野外测试)进行评估。exo - gja1 - 20k处理通过增强线粒体自噬和减少线粒体功能障碍显著改善线粒体质量控制。由NLRP3炎性体驱动的焦亡被显著抑制,NLRP3、ASC和IL-1β表达水平显著降低。行为学分析显示,与对照组相比,exo - gja1 - 20k治疗小鼠在Morris水迷宫中的逃避潜伏期较短,在开阔场测试中的焦虑样行为减少,从而增强了认知表现。重要的是,在pink1敲除小鼠中,exo - gja1 - 20k的治疗作用减弱,强调了对pink1介导的线粒体自噬的依赖。本研究表明,exo - gja1 - 20k通过调节线粒体自噬- nlrp3炎性小体轴,减轻神经炎症,减轻TBI模型的认知缺陷,发挥神经保护作用。这些发现为解决tbi诱导的神经元损伤提出了一种新的治疗策略,并强调了基于ev的治疗神经系统疾病的潜力。
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来源期刊
Translational Stroke Research
Translational Stroke Research CLINICAL NEUROLOGY-NEUROSCIENCES
CiteScore
13.80
自引率
4.30%
发文量
130
审稿时长
6-12 weeks
期刊介绍: Translational Stroke Research covers basic, translational, and clinical studies. The Journal emphasizes novel approaches to help both to understand clinical phenomenon through basic science tools, and to translate basic science discoveries into the development of new strategies for the prevention, assessment, treatment, and enhancement of central nervous system repair after stroke and other forms of neurotrauma. Translational Stroke Research focuses on translational research and is relevant to both basic scientists and physicians, including but not restricted to neuroscientists, vascular biologists, neurologists, neuroimagers, and neurosurgeons.
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