Source:http://linkedlifedata.com/resource/pubmed/id/16280692
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2005-11-10
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pubmed:abstractText |
We previously demonstrated that Actinomycin D (ActD) enhanced HIV-1 replication in the MT-2 cell, a human T-cell leukemia virus type-1-infected cell line. The MT-2 cell is known to produce multiple cytokines spontaneously. In this study, we investigated the impact of ActD on the cytokine production from MT-2 cells and HIV-1 replication in a latently infected cell line, U1. MT-2 cells were pulse-treated with 0 or 200 nM of ActD, and culture supernatants were collected 3 days after incubation. Supernatants from untreated cells (Sup0) induced HIV-1 replication by 150-fold in U1 cells. Culture supernatants from ActD-treated cells (Sup200) enhanced HIV-1 replication by 1200-fold. A combination of a sequential chromatographic approach and mass spectrometric analysis identified that the HIV-inducing factors in Sup200 were interleukin (IL)-6 and tumor necrosis factor (TNF)-beta. Quantitative analysis revealed that ActD treatment increased the concentration of IL-6 in Sup200 by 600% compared with that in Sup0 but decreased the amount of TNFbeta in Sup200 by 85%. Northern blot analysis showed that ActD treatment increased IL-6 transcripts; however, no change was seen in TNFbeta transcripts. These results suggest that ActD induces replication of HIV-1 through modulation of cytokine production.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Dactinomycin,
http://linkedlifedata.com/resource/pubmed/chemical/HIV Core Protein p24,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6,
http://linkedlifedata.com/resource/pubmed/chemical/Lymphotoxin-alpha,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1525-4135
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
40
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
388-97
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16280692-Blotting, Northern,
pubmed-meshheading:16280692-Cell Line,
pubmed-meshheading:16280692-Chromatography,
pubmed-meshheading:16280692-Dactinomycin,
pubmed-meshheading:16280692-HIV Core Protein p24,
pubmed-meshheading:16280692-HIV-1,
pubmed-meshheading:16280692-Humans,
pubmed-meshheading:16280692-Interleukin-6,
pubmed-meshheading:16280692-Lymphotoxin-alpha,
pubmed-meshheading:16280692-Mass Spectrometry,
pubmed-meshheading:16280692-RNA, Messenger,
pubmed-meshheading:16280692-T-Lymphocytes,
pubmed-meshheading:16280692-Transcription, Genetic,
pubmed-meshheading:16280692-Virus Replication
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pubmed:year |
2005
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pubmed:articleTitle |
A transcription inhibitor, actinomycin D, enhances HIV-1 replication through an interleukin-6-dependent pathway.
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pubmed:affiliation |
Laboratory of Human Retrovirology, Science Applications International Corporation (SAIC)-Frederick, Frederick, MD 21702-1201, USA. timamichi@niaid.nih.gov
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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