Source:http://linkedlifedata.com/resource/pubmed/id/19514109
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2009-6-9
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pubmed:abstractText |
It was recently shown that capture of HIV-1 by DC-SIGN-expressing cells and the subsequent transmission of HIV to CD4+ T-lymphocytes can be prevented by carbohydrate-binding agents (CBAs), whereas polyanions were unable to block virus capture by DC-SIGN. In this study, we could show that a short pre-exposure of HIV-1 to both mannose- and N-acetylglucosamine (GlcNAc)-specific CBAs or polyanions dose-dependently prevented virus capture by L-SIGN-expressing 293T-REx/L-SIGN cells and subsequent syncytia formation in co-cultures of the drug-exposed HIV-1-captured 293T-REx/L-SIGN cells and uninfected C8166 CD4+ T-lymphocytes. Additionally, the inhibitory potential of the compounds against L-SIGN-mediated HIV-1 capture and transmission was more pronounced than observed for DC-SIGN expressing293T-REx/DC-SIGN cells. The excess value of CBAs and polyanions to prevent HIV-1 capture and transmission by DC-SIGN and L-SIGN-expressing cells to susceptible T-lymphocytes could be of interest for the development of new drug leads targeting HIV entry/fusion.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anti-HIV Agents,
http://linkedlifedata.com/resource/pubmed/chemical/CLEC4M protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules,
http://linkedlifedata.com/resource/pubmed/chemical/Lectins,
http://linkedlifedata.com/resource/pubmed/chemical/Lectins, C-Type,
http://linkedlifedata.com/resource/pubmed/chemical/Polymers,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface,
http://linkedlifedata.com/resource/pubmed/chemical/polyanions
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1872-9096
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
61-70
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pubmed:meshHeading |
pubmed-meshheading:19514109-Anti-HIV Agents,
pubmed-meshheading:19514109-CD4-Positive T-Lymphocytes,
pubmed-meshheading:19514109-Cell Adhesion Molecules,
pubmed-meshheading:19514109-Cell Line,
pubmed-meshheading:19514109-Dose-Response Relationship, Drug,
pubmed-meshheading:19514109-HIV-1,
pubmed-meshheading:19514109-Humans,
pubmed-meshheading:19514109-Lectins,
pubmed-meshheading:19514109-Lectins, C-Type,
pubmed-meshheading:19514109-Polymers,
pubmed-meshheading:19514109-Receptors, Cell Surface,
pubmed-meshheading:19514109-Virus Attachment
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pubmed:year |
2009
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pubmed:articleTitle |
Capture and transmission of HIV-1 by the C-type lectin L-SIGN (DC-SIGNR) is inhibited by carbohydrate-binding agents and polyanions.
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pubmed:affiliation |
Virology and Chemotherapy, Rega Institute for Medical Research, Katholieke Universiteit Leuven, Leuven, Belgium.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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