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首页> 外文期刊>Human Molecular Genetics >Ibuprofen enhances synaptic function and neural progenitors proliferation markers and improves neuropathology and motor coordination in Machado-Joseph disease models
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Ibuprofen enhances synaptic function and neural progenitors proliferation markers and improves neuropathology and motor coordination in Machado-Joseph disease models

机译:布洛芬增强了突触功能和神经祖细胞增殖标志物,并改善了Machado-Joseph疾病模型中的神经病理学和运动协调

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摘要

Machado-Joseph disease or spinocerebellar ataxia type 3 is an inherited neurodegenerative disease associated with an abnormal glutamine over-repetition within the ataxin-3 protein. This mutant ataxin-3 protein affects several cellular pathways, leading to neuroinflammation and neuronal death in specific brain regions resulting in severe clinical manifestations. Presently, there is no therapy able to modify the disease progression. Nevertheless, anti-inflammatory pharmacological intervention has been associated with positive outcomes in other neurodegenerative diseases. Thus, the present work aimed at investigating whether ibuprofen treatment would alleviate Machado-Joseph disease. We found that ibuprofen-treated mouse models presented a significant reduction in the neuroinflammation markers, namely Il1b and TNFa mRNA and IKB-alpha protein phosphorylation levels. Moreover, these mice exhibited neuronal preservation, cerebellar atrophy reduction, smaller mutant ataxin-3 inclusions and motor performance improvement. Additionally, neural cultures of Machado-Joseph disease patients' induced pluripotent stem cells-derived neural stem cells incubated with ibuprofen showed increased levels of neural progenitors proliferation and synaptic markers such as MSI1, NOTCH1 and SYP. These findings were further confirmed in ibuprofen-treated mice that display increased neural progenitor numbers (Ki67 positive) in the subventricular zone. Furthermore, interestingly, ibuprofen treatment enhanced neurite total length and synaptic function of human neurons. Therefore, our results indicate that ibuprofen reduces neuroinflammation and induces neuroprotection, alleviating Machado-Joseph disease-associated neuropathology and motor impairments. Thus, our findings demonstrate that ibuprofen treatment has the potential to be used as a neuroprotective therapeutic approach in Machado-Joseph disease.
机译:Machado-Joseph病或脊髓小脑共济失调3型是一种遗传性神经退行性疾病,与共济失调3蛋白内异常的谷氨酰胺重复相关。这种突变的ataxin-3蛋白影响多种细胞途径,导致特定脑区的神经炎症和神经元死亡,导致严重的临床表现。目前,还没有能够改变疾病进展的治疗方法。然而,抗炎药物干预与其他神经退行性疾病的积极结果相关。因此,本研究旨在调查布洛芬治疗是否能缓解马查多-约瑟夫病。我们发现,布洛芬治疗的小鼠模型表现出神经炎症标记物,即Il1b和TNFa mRNA以及IKBα蛋白磷酸化水平的显著降低。此外,这些小鼠表现出神经元保护、小脑萎缩减少、较小的突变型共济失调-3内含物和运动能力改善。此外,与布洛芬孵育的Machado-Joseph病患者诱导的多能干细胞衍生的神经干细胞的神经培养显示,神经祖细胞增殖和突触标记物(如MSI1、NOTCH1和SYP)水平增加。这些发现在布洛芬治疗的小鼠中得到进一步证实,这些小鼠的脑室下区神经祖细胞数量增加(Ki67阳性)。此外,有趣的是,布洛芬治疗增强了人类神经元的轴突总长度和突触功能。因此,我们的研究结果表明,布洛芬可以减少神经炎症并诱导神经保护,减轻与Machado-Joseph病相关的神经病理学和运动障碍。因此,我们的研究结果表明,布洛芬治疗有可能被用作Machado-Joseph病的神经保护治疗方法。

著录项

  • 来源
    《Human Molecular Genetics 》 |2019年第22期| 共13页
  • 作者单位

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

    Ohio State Univ Sch Med Res Inst Nationwide Childrens Hosp Columbus OH 43205 USA;

    Univ Coimbra Ctr Neurosci &

    Cell Biol Vectors &

    Gene Therapy Grp P-3004504 Coimbra Portugal;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学遗传学 ;
  • 关键词

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