• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Architecture and regulation of the HIV-1 assembly and holding compartment in macrophages.HIV-1 组装和持留室在巨噬细胞中的结构和调控。
J Virol. 2011 Aug;85(15):7922-7. doi: 10.1128/JVI.00834-11. Epub 2011 May 25.
2
The intracellular plasma membrane-connected compartment in the assembly of HIV-1 in human macrophages.人类巨噬细胞中HIV-1组装过程中与细胞内质膜相连的区室。
BMC Biol. 2016 Jun 23;14:50. doi: 10.1186/s12915-016-0272-3.
3
Organization and regulation of intracellular plasma membrane-connected HIV-1 assembly compartments in macrophages.在巨噬细胞中细胞内质膜连接的 HIV-1 组装隔室的组织和调节。
BMC Biol. 2013 Aug 2;11:89. doi: 10.1186/1741-7007-11-89.
4
HIV-1 assembly in macrophages.HIV-1 在巨噬细胞中的组装。
Retrovirology. 2010 Apr 7;7:29. doi: 10.1186/1742-4690-7-29.
5
In macrophages, HIV-1 assembles into an intracellular plasma membrane domain containing the tetraspanins CD81, CD9, and CD53.在巨噬细胞中,HIV-1组装成一个包含四跨膜蛋白CD81、CD9和CD53的细胞内质膜结构域。
J Cell Biol. 2007 Apr 23;177(2):329-41. doi: 10.1083/jcb.200609050. Epub 2007 Apr 16.
6
Dynamics of HIV-containing compartments in macrophages reveal sequestration of virions and transient surface connections.巨噬细胞中含 HIV 隔室的动力学揭示了病毒粒子的隔离和短暂的表面连接。
PLoS One. 2013 Jul 29;8(7):e69450. doi: 10.1371/journal.pone.0069450. Print 2013.
7
The HIV-1-containing macrophage compartment: a perfect cellular niche?含 HIV-1 的巨噬细胞隔室:完美的细胞生态位?
Trends Microbiol. 2013 Aug;21(8):405-12. doi: 10.1016/j.tim.2013.05.001. Epub 2013 Jun 2.
8
Human macrophages accumulate HIV-1 particles in MHC II compartments.人类巨噬细胞在主要组织相容性复合体II类区室中积累HIV-1颗粒。
Traffic. 2002 Oct;3(10):718-29. doi: 10.1034/j.1600-0854.2002.31004.x.
9
Infectious HIV-1 assembles in late endosomes in primary macrophages.具有传染性的HIV-1在原代巨噬细胞的晚期内体中组装。
J Cell Biol. 2003 Aug 4;162(3):443-55. doi: 10.1083/jcb.200304008. Epub 2003 Jul 28.
10
Siglec-1 initiates formation of the virus-containing compartment and enhances macrophage-to-T cell transmission of HIV-1.唾液酸结合免疫球蛋白样凝集素-1启动含病毒区室的形成,并增强HIV-1从巨噬细胞到T细胞的传播。
PLoS Pathog. 2017 Jan 27;13(1):e1006181. doi: 10.1371/journal.ppat.1006181. eCollection 2017 Jan.

引用本文的文献

1
Negative interplay between HIV-1 Gag and amyloid precursor protein centers around competition for VPS4A and TSG101.HIV-1 核衣壳蛋白(Gag)与淀粉样前体蛋白之间的负相互作用主要围绕对VPS4A和TSG101的竞争。
Proc Natl Acad Sci U S A. 2025 Aug 26;122(34):e2503988122. doi: 10.1073/pnas.2503988122. Epub 2025 Aug 21.
2
CD4+ T cells facilitate replication of primary HIV-1 strains in macrophages and formation of macrophage internal virus-containing compartments.CD4 + T细胞促进原发性HIV-1毒株在巨噬细胞中的复制以及巨噬细胞内病毒包涵体的形成。
J Virol. 2025 Apr 15;99(4):e0018225. doi: 10.1128/jvi.00182-25. Epub 2025 Mar 25.
3
The CLIC/GEEC pathway regulates particle uptake and formation of the virus-containing compartment (VCC) in HIV-1-infected macrophages.CLIC/GEEC途径调节HIV-1感染的巨噬细胞中颗粒摄取和含病毒区室(VCC)的形成。
PLoS Pathog. 2025 Mar 11;21(3):e1012564. doi: 10.1371/journal.ppat.1012564. eCollection 2025 Mar.
4
HIV-1 N-myristoylation-dependent hijacking of late endosomes/lysosomes to drive Gag assembly in macrophages.HIV-1 N-豆蔻酰化依赖性晚期内体/溶酶体劫持驱动巨噬细胞中的 Gag 组装。
J Cell Sci. 2024 Nov 15;137(22). doi: 10.1242/jcs.263588. Epub 2024 Nov 21.
5
HIV-1 promotes ubiquitination of the amyloidogenic C-terminal fragment of APP to support viral replication.HIV-1 促进淀粉样前体蛋白 C 端片段的泛素化,以支持病毒复制。
Nat Commun. 2023 Jul 15;14(1):4227. doi: 10.1038/s41467-023-40000-x.
6
Urokinase plasminogen activator surface receptor restricts HIV-1 replication by blocking virion release from the cell membrane.尿激酶型纤溶酶原激活物表面受体通过阻止病毒粒子从细胞膜释放来限制 HIV-1 的复制。
Proc Natl Acad Sci U S A. 2023 Jan 17;120(3):e2212991120. doi: 10.1073/pnas.2212991120. Epub 2023 Jan 13.
7
Co-receptor signaling in the pathogenesis of neuroHIV.共受体信号在神经 HIV 发病机制中的作用。
Retrovirology. 2021 Aug 24;18(1):24. doi: 10.1186/s12977-021-00569-x.
8
How HIV-1 Gag Manipulates Its Host Cell Proteins: A Focus on Interactors of the Nucleocapsid Domain.HIV-1 Gag 如何操纵宿主细胞蛋白:重点关注核衣壳域的相互作用蛋白。
Viruses. 2020 Aug 13;12(8):888. doi: 10.3390/v12080888.
9
Macrophage Cell-Cell Interactions Promoting HIV-1 Infection.巨噬细胞细胞间相互作用促进 HIV-1 感染。
Viruses. 2020 Apr 28;12(5):492. doi: 10.3390/v12050492.
10
Effect of Human Immunodeficiency Virus on Trace Elements in the Brain.人类免疫缺陷病毒对大脑中微量元素的影响。
Biol Trace Elem Res. 2021 Jan;199(1):41-52. doi: 10.1007/s12011-020-02129-4. Epub 2020 Apr 1.

本文引用的文献

1
3D visualization of HIV transfer at the virological synapse between dendritic cells and T cells.HIV 在树突状细胞和 T 细胞间病毒学突触处转移的 3D 可视化。
Proc Natl Acad Sci U S A. 2010 Jul 27;107(30):13336-41. doi: 10.1073/pnas.1003040107. Epub 2010 Jul 12.
2
Role of macrophages in HIV infection and persistence.巨噬细胞在 HIV 感染和持续感染中的作用。
Expert Rev Clin Immunol. 2006 Jul;2(4):613-26. doi: 10.1586/1744666X.2.4.613.
3
Molecular mechanisms of HIV-1 persistence in the monocyte-macrophage lineage.HIV-1 在单核细胞-巨噬细胞谱系中持续存在的分子机制。
Retrovirology. 2010 Apr 9;7:32. doi: 10.1186/1742-4690-7-32.
4
HIV-1 assembly in macrophages.HIV-1 在巨噬细胞中的组装。
Retrovirology. 2010 Apr 7;7:29. doi: 10.1186/1742-4690-7-29.
5
Macrophages: do they impact AIDS progression more than CD4 T cells?巨噬细胞:它们比 CD4 T 细胞对艾滋病进展的影响更大吗?
J Leukoc Biol. 2010 Apr;87(4):569-73. doi: 10.1189/jlb.0909626. Epub 2010 Jan 6.
6
Ion-abrasion scanning electron microscopy reveals surface-connected tubular conduits in HIV-infected macrophages.离子研磨扫描电子显微镜显示,HIV 感染的巨噬细胞存在表面相连的管状导管。
PLoS Pathog. 2009 Sep;5(9):e1000591. doi: 10.1371/journal.ppat.1000591. Epub 2009 Sep 25.
7
HIV interactions with monocytes and dendritic cells: viral latency and reservoirs.人类免疫缺陷病毒与单核细胞和树突状细胞的相互作用:病毒潜伏期与病毒储存库
Retrovirology. 2009 Jun 1;6:51. doi: 10.1186/1742-4690-6-51.
8
Mechanisms of endocytosis.内吞作用的机制。
Annu Rev Biochem. 2009;78:857-902. doi: 10.1146/annurev.biochem.78.081307.110540.
9
Evidence that productive human immunodeficiency virus type 1 assembly can occur in an intracellular compartment.有证据表明,有生产性的1型人类免疫缺陷病毒组装可在细胞内区室中发生。
J Virol. 2009 Jun;83(11):5375-87. doi: 10.1128/JVI.00109-09. Epub 2009 Mar 18.
10
HIV assembly and budding in macrophages.
Biochem Soc Trans. 2009 Feb;37(Pt 1):185-9. doi: 10.1042/BST0370185.

HIV-1 组装和持留室在巨噬细胞中的结构和调控。

Architecture and regulation of the HIV-1 assembly and holding compartment in macrophages.

机构信息

EMBL, Meyerhofstrasse 1, D-69117 Heidelberg, Germany.

出版信息

J Virol. 2011 Aug;85(15):7922-7. doi: 10.1128/JVI.00834-11. Epub 2011 May 25.

DOI:10.1128/JVI.00834-11
PMID:21613397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3147899/
Abstract

Productive infection of macrophages is central to HIV-1 pathogenesis. Newly formed virions bud into a tubular membranous compartment that is contiguous with the plasma membrane. However, little is known about the structure of this compartment and its potential regulation by infection. Here we characterized this compartment in macrophages using electron tomography and electron microscopy with stereology. We found an intricate, interconnected membrane network that constitutes a preexisting physiologic structure in macrophages but which expands in size upon HIV-1 infection. Membranes required for this expansion were apparently derived from preexisting pools of plasma membrane. Physical connections between this compartment and the extracellular milieu were frequently made by tube-like structures of insufficient diameter for virion passage. We conclude that HIV-1 induces the expansion of a complex membranous labyrinth in macrophages in which the virus buds and can be retained, with potential consequences for transmission and immune evasion.

摘要

巨噬细胞的有效感染是 HIV-1 发病机制的核心。新形成的病毒粒子出芽到与质膜连续的管状膜隔室中。然而,人们对该隔室的结构及其感染时的潜在调节知之甚少。在这里,我们使用电子断层扫描和电子显微镜体视学来描述巨噬细胞中的这个隔室。我们发现了一个复杂的、相互连接的膜网络,它构成了巨噬细胞中预先存在的生理结构,但在 HIV-1 感染时会扩大。这种扩张所需的膜显然来自于预先存在的质膜池。这个隔室与细胞外环境之间的物理连接通常是通过直径不足以让病毒粒子通过的管状结构来实现的。我们得出结论,HIV-1 诱导巨噬细胞中复杂的膜迷路扩张,病毒在其中出芽并可以被保留,这可能对传播和免疫逃避产生影响。