人类免疫缺陷病毒相关性痴呆症:病毒蛋白积累与神经元变性之间的联系。

Current trends in neurology Pub Date : 2014-01-01
Italo Mocchetti, Alessia Bachis, Giuseppe Esposito, Scott R Turner, Francesca Taraballi, Ennio Tasciotti, Mikell Paige, Valeriya Avdoshina
{"title":"人类免疫缺陷病毒相关性痴呆症:病毒蛋白积累与神经元变性之间的联系。","authors":"Italo Mocchetti, Alessia Bachis, Giuseppe Esposito, Scott R Turner, Francesca Taraballi, Ennio Tasciotti, Mikell Paige, Valeriya Avdoshina","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>In the late stage of human immunodeficiency virus-1 (HIV) infection, a subset of individuals develops HIV associated neurocognitive disorders (HAND), which in its severe form, is characterized by motor and cognitive dysfunction. Dendritic pruning, synaptic abnormalities and neuronal apoptosis are observed in these patients. There are numerous advances in our understanding of HIV interactions with cells of the central nervous system. However, the underlying causes of neurological symptoms and pathological alterations observed in HIV positive subjects are poorly understood. Moreover, little is still known about the molecular mechanisms by which HIV induces synaptic dysfunction and degeneration. HAND resembles other common neurological diseases such as Alzheimer's and Huntington's diseases. These neurodegenerative disorders are characterized by accumulation of toxic proteins such as tau and huntingtin, respectively, which promote axonal degeneration by impairing axonal transport. Axonal degeneration precedes neuronal death. Therefore, a better understanding of the mechanisms whereby HIV triggers axonal degeneration has potential implications for developing therapeutic compounds to prevent synaptic failure in HAND. This article highlights and reviews evidence showing that neuronal accumulation of viral proteins promotes axonal damage.</p>","PeriodicalId":72761,"journal":{"name":"Current trends in neurology","volume":"8 ","pages":"71-85"},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4461001/pdf/nihms692701.pdf","citationCount":"0","resultStr":"{\"title\":\"Human immunodeficiency virus-associated dementia: a link between accumulation of viral proteins and neuronal degeneration.\",\"authors\":\"Italo Mocchetti, Alessia Bachis, Giuseppe Esposito, Scott R Turner, Francesca Taraballi, Ennio Tasciotti, Mikell Paige, Valeriya Avdoshina\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In the late stage of human immunodeficiency virus-1 (HIV) infection, a subset of individuals develops HIV associated neurocognitive disorders (HAND), which in its severe form, is characterized by motor and cognitive dysfunction. Dendritic pruning, synaptic abnormalities and neuronal apoptosis are observed in these patients. There are numerous advances in our understanding of HIV interactions with cells of the central nervous system. However, the underlying causes of neurological symptoms and pathological alterations observed in HIV positive subjects are poorly understood. Moreover, little is still known about the molecular mechanisms by which HIV induces synaptic dysfunction and degeneration. HAND resembles other common neurological diseases such as Alzheimer's and Huntington's diseases. These neurodegenerative disorders are characterized by accumulation of toxic proteins such as tau and huntingtin, respectively, which promote axonal degeneration by impairing axonal transport. Axonal degeneration precedes neuronal death. Therefore, a better understanding of the mechanisms whereby HIV triggers axonal degeneration has potential implications for developing therapeutic compounds to prevent synaptic failure in HAND. This article highlights and reviews evidence showing that neuronal accumulation of viral proteins promotes axonal damage.</p>\",\"PeriodicalId\":72761,\"journal\":{\"name\":\"Current trends in neurology\",\"volume\":\"8 \",\"pages\":\"71-85\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4461001/pdf/nihms692701.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current trends in neurology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current trends in neurology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

在人类免疫缺陷病毒-1(HIV)感染的晚期,一部分人会出现 HIV 相关神经认知障碍(HAND),严重者会出现运动和认知功能障碍。在这些患者身上可以观察到树突修剪、突触异常和神经元凋亡。我们对艾滋病病毒与中枢神经系统细胞相互作用的认识取得了许多进展。然而,我们对艾滋病毒阳性患者的神经症状和病理改变的根本原因还知之甚少。此外,我们对艾滋病病毒诱发突触功能障碍和退化的分子机制也知之甚少。HAND 类似于其他常见的神经系统疾病,如阿尔茨海默氏症和亨廷顿氏症。这些神经退行性疾病的特征分别是有毒蛋白质(如 tau 和亨廷顿蛋白)的积累,它们通过损害轴突运输促进轴突变性。轴突变性先于神经元死亡。因此,更好地了解艾滋病病毒引发轴突变性的机制,对于开发治疗化合物以预防手足口病的突触衰竭具有潜在的意义。本文重点介绍并回顾了有证据表明神经元中病毒蛋白的积累会促进轴突损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

摘要图片

摘要图片

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Human immunodeficiency virus-associated dementia: a link between accumulation of viral proteins and neuronal degeneration.

In the late stage of human immunodeficiency virus-1 (HIV) infection, a subset of individuals develops HIV associated neurocognitive disorders (HAND), which in its severe form, is characterized by motor and cognitive dysfunction. Dendritic pruning, synaptic abnormalities and neuronal apoptosis are observed in these patients. There are numerous advances in our understanding of HIV interactions with cells of the central nervous system. However, the underlying causes of neurological symptoms and pathological alterations observed in HIV positive subjects are poorly understood. Moreover, little is still known about the molecular mechanisms by which HIV induces synaptic dysfunction and degeneration. HAND resembles other common neurological diseases such as Alzheimer's and Huntington's diseases. These neurodegenerative disorders are characterized by accumulation of toxic proteins such as tau and huntingtin, respectively, which promote axonal degeneration by impairing axonal transport. Axonal degeneration precedes neuronal death. Therefore, a better understanding of the mechanisms whereby HIV triggers axonal degeneration has potential implications for developing therapeutic compounds to prevent synaptic failure in HAND. This article highlights and reviews evidence showing that neuronal accumulation of viral proteins promotes axonal damage.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Peripheral modulation of chronic visceral pain. Neural reorganization associated with visceral pain. Visceral nociception and functional diseases. Arousal and the control of perception and movement. Human immunodeficiency virus-associated dementia: a link between accumulation of viral proteins and neuronal degeneration.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1