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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1994-1-12
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pubmed:abstractText |
Infection by influenza A virus has previously been shown to prime macrophages for a high TNF-alpha production. Influenza A virus induced a TNF-alpha mRNA accumulation that consisted of two types: a regular 1.7 kb and an additional high m.w. 2.4 kb species in murine macrophages, and a high m.w. 3.6 kb species in human monocytes. In this study, we further characterized this virus-induced, novel high m.w. TNF-alpha mRNA. The additional high m.w. TNF-alpha mRNA represented a true polyadenylated mRNA and its induction required exposure to infectious viruses. The regular and the high m.w. TNF-alpha mRNA were both found in the nuclear fraction and the cytoplasm. We excluded that the novel high m.w. TNF-alpha mRNA was an intron-containing precursor TNF-alpha mRNA that could have persisted in virus-infected macrophages. When TNF-alpha exons 1 to 4 and TNF-alpha exons 2 to 4 were amplified by polymerase chain reaction, only regular and no high m.w. bands were detected. By use of specific TNF-alpha intron I and intron III cDNA we could definitely demonstrate the absence of introns in the high m.w. TNF-alpha mRNA. The high m.w. TNF-alpha mRNA was free of TNF-beta and TNF intergenic region elements but contained the 5' and 3' untranslated region of TNF-alpha. Influenza A virus infection also induced a double band of IL-1 beta and IL-6 mRNA. Whether this novel high m.w. TNF-alpha mRNA represents a virus-induced abnormality or a superinduction of an otherwise normal but minor TNF-alpha transcript, and whether this high m.w. TNF-alpha mRNA species codes for a biologically active product, remains to be examined.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
152
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
280-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7902856-Animals,
pubmed-meshheading:7902856-Base Sequence,
pubmed-meshheading:7902856-Cell Line,
pubmed-meshheading:7902856-Cell Nucleus,
pubmed-meshheading:7902856-Cytoplasm,
pubmed-meshheading:7902856-Gene Expression Regulation,
pubmed-meshheading:7902856-Humans,
pubmed-meshheading:7902856-Influenza A virus,
pubmed-meshheading:7902856-Macrophages,
pubmed-meshheading:7902856-Mice,
pubmed-meshheading:7902856-Molecular Sequence Data,
pubmed-meshheading:7902856-Molecular Weight,
pubmed-meshheading:7902856-Poly A,
pubmed-meshheading:7902856-Polymerase Chain Reaction,
pubmed-meshheading:7902856-RNA, Messenger,
pubmed-meshheading:7902856-Tumor Necrosis Factor-alpha
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pubmed:year |
1994
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pubmed:articleTitle |
Characterization of a high molecular weight tumor necrosis factor-alpha mRNA in influenza A virus-infected macrophages.
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pubmed:affiliation |
Institute of Immunology, Philipps University, Marburg, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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