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PMID: 2298923 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Human immunodeficiency virus-1 infection of macrophages in vitro neither induces tumor necrosis factor (TNF)/cachectin gene expression nor alters TNF/cachectin induction by lipopolysaccharide.

The Journal of clinical investigation ·Vol. 85 ·No. 2 ·1990-02-00 ·Pages 591-6

Munis JR, Richman DD, Kornbluth RS

Abstract

The synthesis of tumor necrosis factor (TNF)/cachectin was assessed in primary monocyte-derived macrophage (MDM) cultures after in vitro infection with a macrophage-tropic strain of HIV-1 (HTLV-IIIBa-L/85). Productive and cytopathic infections in MDM cultures were established using a high multiplicity of infection (m.o.i. = 3) under conditions that minimized endotoxin contamination. Culture supernatants were tested for TNF/cachectin activity by L929 cell cytotoxicity assay, and TNF/cachectin mRNA was assessed by a sensitive PCR amplification technique that could detect between 1 and 10 cells fully activated for TNF/cachectin expression. Unstimulated MDM cultures produced no detectable levels of TNF/cachectin activity or mRNA, consistent with previous demonstrations that production of this cytokine by macrophages is an inducible and not a constitutive event. HIV-1 infection failed to induce detectable TNF/cachectin activity or mRNA in these unstimulated cultures. In addition, the responsiveness of macrophages to lipopolysaccharide (LPS) induction of TNF/cachectin production was assessed in dose-response and kinetic experiments. No differences between infected and uninfected cultures were discernable. These results demonstrate that productive and cytopathic infection with a macrophage-tropic strain of HIV-1 does not alter the regulation of TNF/cachectin expression in macrophages.

MeSH Terms
Cells, Cultured Dose-Response Relationship, Drug Gene Expression HIV-1/pathogenicity Humans Lipopolysaccharides/pharmacology Macrophages/metabolism Polymerase Chain Reaction RNA, Messenger/analysis Tumor Necrosis Factor-alpha/biosynthesis,genetics
Chemicals
Lipopolysaccharides RNA, Messenger Tumor Necrosis Factor-alpha
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Munis J R
Department of Medicine, University of California, San Diego.
Richman D D
Kornbluth R S
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Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1990-02-00
Pages
591-6
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC296464
Subset
IM
Grants
NIAID NIH HHS · AI-25316 · United States
NIAID NIH HHS · AI-52578 · United States
NIAID NIH HHS · AI-62548 · United States
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