Extracellular vesicles produced by HIV-1 Nef-expressing cells induce myelin impairment and oligodendrocyte damage in the mouse central nervous system.

IF 9.3 1区 医学 Q1 IMMUNOLOGY
Jessica K Schenck, Molly T Karl, Cheryl Clarkson-Paredes, Ashley Bastin, Tatiana Pushkarsky, Beda Brichacek, Robert H Miller, Michael I Bukrinsky
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Abstract

HIV-associated neurocognitive disorders (HAND) are a spectrum of cognitive impairments that continue to affect approximately half of all HIV-positive individuals despite effective viral suppression through antiretroviral therapy (ART). White matter pathologies have persisted in the ART era, and the degree of white matter damage correlates with the degree of neurocognitive impairment in patients with HAND. The HIV protein Nef has been implicated in HAND pathogenesis, but its effect on white matter damage has not been well characterized. Here, utilizing in vivo, ex vivo, and in vitro methods, we demonstrate that Nef-containing extracellular vesicles (Nef EVs) disrupt myelin sheaths and inflict damage upon oligodendrocytes within the murine central nervous system. Intracranial injection of Nef EVs leads to reduced myelin basic protein (MBP) staining and a decreased number of CC1 + oligodendrocytes in the corpus callosum. Moreover, cerebellar slice cultures treated with Nef EVs exhibit diminished MBP expression and increased presence of unmyelinated axons. Primary mixed brain cultures and enriched oligodendrocyte precursor cell cultures exposed to Nef EVs display a decreased number of O4 + cells, indicative of oligodendrocyte impairment. These findings underscore the potential contribution of Nef EV-mediated damage to oligodendrocytes and myelin maintenance in the pathogenesis of HAND.

表达HIV-1 Nef的细胞产生的胞外囊泡会诱发小鼠中枢神经系统的髓鞘损伤和少突胶质细胞损伤。
艾滋病相关神经认知障碍(HAND)是一系列认知障碍,尽管通过抗逆转录病毒疗法(ART)有效抑制了病毒,但仍有大约一半的艾滋病病毒抗体阳性患者受到影响。白质病变在抗逆转录病毒疗法时代依然存在,白质损伤程度与 HAND 患者的神经认知障碍程度相关。艾滋病毒蛋白 Nef 与手足口病的发病机制有关,但其对白质损伤的影响尚未得到很好的描述。在这里,我们利用体内、体外和体外方法证明,在小鼠中枢神经系统中,含有 Nef 的细胞外囊泡 (Nef EVs) 会破坏髓鞘并对少突胶质细胞造成损伤。颅内注射 Nef EVs 会导致胼胝体中髓鞘碱性蛋白(MBP)染色减少和 CC1 + 少突胶质细胞数量减少。此外,用 Nef EVs 处理的小脑切片培养物显示 MBP 表达减少,无髓鞘轴突增多。暴露于 Nef EVs 的原代混合脑培养物和富集的少突胶质细胞前体细胞培养物显示 O4 + 细胞数量减少,表明少突胶质细胞受损。这些发现强调了Nef EV介导的对少突胶质细胞和髓鞘维持的损伤在HAND发病机制中的潜在作用。
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来源期刊
Journal of Neuroinflammation
Journal of Neuroinflammation 医学-神经科学
CiteScore
15.90
自引率
3.20%
发文量
276
审稿时长
1 months
期刊介绍: The Journal of Neuroinflammation is a peer-reviewed, open access publication that emphasizes the interaction between the immune system, particularly the innate immune system, and the nervous system. It covers various aspects, including the involvement of CNS immune mediators like microglia and astrocytes, the cytokines and chemokines they produce, and the influence of peripheral neuro-immune interactions, T cells, monocytes, complement proteins, acute phase proteins, oxidative injury, and related molecular processes. Neuroinflammation is a rapidly expanding field that has significantly enhanced our knowledge of chronic neurological diseases. It attracts researchers from diverse disciplines such as pathology, biochemistry, molecular biology, genetics, clinical medicine, and epidemiology. Substantial contributions to this field have been made through studies involving populations, patients, postmortem tissues, animal models, and in vitro systems. The Journal of Neuroinflammation consolidates research that centers around common pathogenic processes. It serves as a platform for integrative reviews and commentaries in this field.
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