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A 3-O-sulfated heparan sulfate binding peptide preferentially targets herpes simplex virus 2-infected cells.一种 3-O-硫酸化肝素硫酸结合肽优先靶向单纯疱疹病毒 2 感染的细胞。
J Virol. 2012 Jun;86(12):6434-43. doi: 10.1128/JVI.00433-12. Epub 2012 Apr 4.
2
Prevalence of Neisseria gonorrhoeae infections among men and women entering the National Job Training Program--United States, 2004-2009.2004-2009 年美国国家职业培训计划中进入人员的淋病奈瑟菌感染率——男性和女性。
Sex Transm Dis. 2012 Jan;39(1):49-54. doi: 10.1097/OLQ.0b013e318231cd5d.
3
Syphilis: using modern approaches to understand an old disease.梅毒:用现代方法理解古老疾病。
J Clin Invest. 2011 Dec;121(12):4584-92. doi: 10.1172/JCI57173. Epub 2011 Dec 1.
4
Preventing sexually transmitted infections: back to basics.预防性传播感染:回归基础。
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Molecular functions of syndecan-1 in disease.黏附素-1 的分子功能与疾病。
Matrix Biol. 2012 Jan;31(1):3-16. doi: 10.1016/j.matbio.2011.10.001. Epub 2011 Oct 18.
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An important role for syndecan-1 in herpes simplex virus type-1 induced cell-to-cell fusion and virus spread.硫酸乙酰肝素蛋白聚糖-1 在单纯疱疹病毒 1 诱导的细胞间融合和病毒传播中具有重要作用。
PLoS One. 2011;6(9):e25252. doi: 10.1371/journal.pone.0025252. Epub 2011 Sep 21.
7
Heparan sulfate binding by natural eastern equine encephalitis viruses promotes neurovirulence.天然东部马脑炎病毒通过肝素结合促进神经毒力。
Proc Natl Acad Sci U S A. 2011 Sep 20;108(38):16026-31. doi: 10.1073/pnas.1110617108. Epub 2011 Sep 6.
8
Anti-heparan sulfate peptides that block herpes simplex virus infection in vivo.抗肝素硫酸盐肽可阻断体内单纯疱疹病毒感染。
J Biol Chem. 2011 Jul 15;286(28):25406-15. doi: 10.1074/jbc.M110.201103. Epub 2011 May 19.
9
HIV-1 p17 matrix protein interacts with heparan sulfate side chain of CD44v3, syndecan-2, and syndecan-4 proteoglycans expressed on human activated CD4+ T cells affecting tumor necrosis factor alpha and interleukin 2 production.HIV-1 p17 基质蛋白与人活化的 CD4+T 细胞表面表达的 CD44v3、 syndecan-2 和 syndecan-4 蛋白聚糖的肝素硫酸盐侧链相互作用,影响肿瘤坏死因子α和白细胞介素 2 的产生。
J Biol Chem. 2011 Jun 3;286(22):19541-8. doi: 10.1074/jbc.M110.191270. Epub 2011 Apr 11.
10
Single particle tracking confirms that multivalent Tat protein transduction domain-induced heparan sulfate proteoglycan cross-linkage activates Rac1 for internalization.单颗粒示踪技术证实,多价 Tat 蛋白转导结构域诱导的硫酸乙酰肝素蛋白聚糖交联激活 Rac1 进行内化。
J Biol Chem. 2011 Mar 25;286(12):10581-92. doi: 10.1074/jbc.M110.187450. Epub 2011 Jan 3.

硫酸乙酰肝素在性传播感染中的作用。

Role of heparan sulfate in sexually transmitted infections.

机构信息

Department of Microbiology and Immunology, Chicago College of Osteopathic Medicine, Midwestern University, Downers Grove, IL 60515, USA.

出版信息

Glycobiology. 2012 Nov;22(11):1402-12. doi: 10.1093/glycob/cws106. Epub 2012 Jul 6.

DOI:10.1093/glycob/cws106
PMID:22773448
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3481906/
Abstract

Cell surface heparan sulfate (HS), a polysaccharide composed of alternating uronic acid and glucosamine residues, represents a common link that many sexually transmitted infections (STIs) require for infection. Variable modifications within the monomeric units of HS chains together with their unique structural conformations generate heterogeneity, which expands the ability of HS to bind a diverse array of host and microbial proteins. Recent advances made in the field of glycobiology have critically enhanced our understanding of HS and its interactions with microbes and their significance in important human diseases. The role of HS has been elaborated for several STIs to include those caused by herpes simplex virus, human immunodeficiency virus, human papillomavirus, and Chlamydia. In addition, gonorrhea, syphilis, and yeast infections are also dependent on the presence of HS on human target cells. Critical steps such as pathogen adhesion or binding to host cells followed by internalization to enhance intracellular survival and possible spread to other cells are mediated by HS. In addition, HS guided cell signaling plays a role in the development of angiogenesis and inflammation associated with many STIs. Past and ongoing investigations are providing new push for the development of HS-mimetics and analogs as novel prevention strategies against many different STIs. This review article summarizes the significance of HS in STIs and describes how emerging new products that target HS can be used to control the spread of STIs.

摘要

细胞表面硫酸乙酰肝素 (HS) 是一种由交替的糖醛酸和葡萄糖胺残基组成的多糖,它代表了许多性传播感染 (STIs) 感染所需的共同联系。HS 链单体单元内的可变修饰及其独特的结构构象产生了异质性,从而扩大了 HS 与多种宿主和微生物蛋白结合的能力。糖生物学领域的最新进展极大地提高了我们对 HS 及其与微生物相互作用的理解,以及它们在重要人类疾病中的重要性。HS 的作用已在几种 STIs 中得到阐述,包括单纯疱疹病毒、人类免疫缺陷病毒、人乳头瘤病毒和衣原体引起的感染。此外,淋病、梅毒和酵母感染也依赖于人类靶细胞上 HS 的存在。HS 介导了病原体与宿主细胞的黏附和内化等关键步骤,从而增强了细胞内的存活和可能向其他细胞的传播。此外,HS 指导的细胞信号转导在许多 STIs 相关的血管生成和炎症发展中发挥作用。过去和正在进行的研究为开发 HS 类似物和类似物作为许多不同 STIs 的新型预防策略提供了新的动力。本文综述了 HS 在 STIs 中的重要性,并描述了针对 HS 的新兴新产品如何用于控制 STIs 的传播。