Source:http://linkedlifedata.com/resource/pubmed/id/20667598
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
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pubmed:dateCreated |
2010-11-24
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pubmed:abstractText |
Massive aggregations of macrophages are frequently detected in afflicted lungs of patients with severe acute respiratory syndrome-associated coronavirus (SARS-CoV) infection. In vitro, ectopic expression of transcription factors, in particular CCAAT/enhancer-binding protein alpha (C/EBP?) and C/EBP?, can convert B cells into functional macrophages. However, little is known about the specific ligands responsible for such phenotype conversion. Here, we investigated whether spike protein of SARS-CoV can act as a ligand to trigger the conversion of B cells to macrophages. We transduced SARS-CoV spike protein-displayed recombinant baculovirus (SSDRB), vAtEpGS688, into peripheral B cells and B lymphoma cells. Cell surface expression of CD19 or Mac-1 (CD11b) was determined by flow cytometry. SSDRB-mediated changes in gene expression profiles of B lymphoma cells were analyzed by microarray. In this report, we showed that spike protein of SARS virus could induce phenotypic conversion of human B cells, either from peripheral blood or B lymphoma cells, to macrophage-like cells that were steadily losing the B-cell marker CD19 and in turn expressing the macrophage-specific marker Mac-1. Furthermore, we found that SSDRB enhanced the expression of CD86, hypoxia-inducible factor-1? (HIF1?), suppressor of cytokine signaling (SOCS or STAT-induced STAT inhibitor)-3, C/EBP?, insulin-like growth factor-binding protein 3 (IGFBP3), Krüpple-like factor (KLF)-5, and CD54, without marked influence on C/EBP? or PU.1 expression in transduced cells. Prolonged exposure to hypoxia could also induce macrophage-like conversion of B cells. These macrophage-like cells were defective in phagocytosis of red fluorescent beads. In conclusion, our results suggest that conversion of B cells to macrophage-like cells, similar to a pathophysiological response, could be mediated by a devastating viral ligand, in particular spike protein of SARS virus, or in combination with severe local hypoxia, which is a condition often observed in afflicted lungs of SARS patients.
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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/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Envelope Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/spike glycoprotein, coronavirus
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1872-9142
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010 Elsevier Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2575-86
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pubmed:meshHeading |
pubmed-meshheading:20667598-Animals,
pubmed-meshheading:20667598-B-Lymphocytes,
pubmed-meshheading:20667598-Cell Line,
pubmed-meshheading:20667598-Gene Expression Profiling,
pubmed-meshheading:20667598-Humans,
pubmed-meshheading:20667598-Lymphoma, B-Cell,
pubmed-meshheading:20667598-Macrophages,
pubmed-meshheading:20667598-Male,
pubmed-meshheading:20667598-Membrane Glycoproteins,
pubmed-meshheading:20667598-Mice,
pubmed-meshheading:20667598-Mice, Inbred BALB C,
pubmed-meshheading:20667598-Phenotype,
pubmed-meshheading:20667598-Recombinant Proteins,
pubmed-meshheading:20667598-SARS Virus,
pubmed-meshheading:20667598-Viral Envelope Proteins
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pubmed:year |
2010
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pubmed:articleTitle |
SARS spike protein induces phenotypic conversion of human B cells to macrophage-like cells.
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pubmed:affiliation |
Graduate Institute of Microbiology and Public Health, National Chung Hsing University, 250 Kuo Kuang Road, Taichung 40227, Taiwan.
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pubmed:publicationType |
Journal Article
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