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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007589,
umls-concept:C0019691,
umls-concept:C0019704,
umls-concept:C0024432,
umls-concept:C0033684,
umls-concept:C0079189,
umls-concept:C0086418,
umls-concept:C0871261,
umls-concept:C1321301,
umls-concept:C1511938,
umls-concept:C1621633,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C1709059,
umls-concept:C2911692
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pubmed:issue |
1
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pubmed:dateCreated |
1997-8-7
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pubmed:abstractText |
We previously reported that in vitro culture of human peripheral blood monocytes resulted in a time-dependent differentiation into macrophages and in an enhanced capacity for producing certain cytokines [i.e., tumor necrosis factor alpha, interleukin-6 (IL-6), and interferon-beta (IFN-beta)] in response to bacterial lipopolysaccharide (LPS). HIV-1 infection or gp120 treatment of monocyte/macrophages resulted in the induction of low levels of IFN-beta, which were very effective in restricting viral replication in 7-day cultured macrophages but not in freshly isolated cells. This enhanced response of macrophages was due to a higher sensitivity of these cells to the antiviral effect of IFN-beta. Consistent with this finding, 7-day cultured macrophages exhibited higher levels of type I IFN receptors than 1-day cultured monocytes. Treatment of monocyte/macrophages with gp120 also caused a marked increase in IL-10 secretion, regardless of the differentiation state. No IL-12 secretion was detected in monocyte/macrophage cultures treated with gp120 alone. However, consistent IL-12 secretion was found in 7-day cultured macrophages primed with IFN-beta and subsequently stimulated with gp120. Macrophages responded more efficiently than monocytes to the priming effect of IFN-beta for IL-12 production. This was consistent with a stronger antiviral response against vesicular stomatitis virus by these cells as well as with a higher expression of IFN-beta receptors. The finding that the acquisition of the macrophage phenotype is associated with an increased capacity to respond to environmental signals (such as type I and type II IFNs) underlines the importance of the differentiation process for the selection of a certain repertoire of responses that may allow these cells to have important functions in vivo.
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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/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Envelope Protein gp120,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-beta,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interferon
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0741-5400
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
62
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
49-53
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:9225992-Cell Differentiation,
pubmed-meshheading:9225992-Cells, Cultured,
pubmed-meshheading:9225992-Cytokines,
pubmed-meshheading:9225992-HIV Envelope Protein gp120,
pubmed-meshheading:9225992-HIV-1,
pubmed-meshheading:9225992-Humans,
pubmed-meshheading:9225992-Immunophenotyping,
pubmed-meshheading:9225992-Interferon-beta,
pubmed-meshheading:9225992-Interferon-gamma,
pubmed-meshheading:9225992-Interleukin-10,
pubmed-meshheading:9225992-Interleukin-12,
pubmed-meshheading:9225992-Lipopolysaccharides,
pubmed-meshheading:9225992-Macrophages,
pubmed-meshheading:9225992-Models, Immunological,
pubmed-meshheading:9225992-Monocytes,
pubmed-meshheading:9225992-Receptors, Interferon,
pubmed-meshheading:9225992-Virus Replication
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pubmed:year |
1997
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pubmed:articleTitle |
Induction of cytokines by HIV-1 and its gp120 protein in human peripheral blood monocyte/macrophages and modulation of cytokine response during differentiation.
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pubmed:affiliation |
Laboratory of Virology, Istituto Superiore di Sanità, Rome, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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