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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1991-9-18
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pubmed:abstractText |
In vivo exposure of female B6C3F1 mice to gallium arsenide (GaAs) was evaluated for its effect on the in vitro IgM antibody-forming cell (AFC) response. In vivo exposure to a single intratracheal dose of GaAs (2.5-200 mg/kg) resulted in a dose-dependent decrease in the in vitro IgM AFC response to the T-dependent antigen sheep red blood cells (SRBC) with a 97% decrease at 200 mg/kg when compared to vehicle controls. The response to the T-independent antigen DNP-Ficoll was significantly reduced at 100 and 200 mg/kg. Spleen cellularity decreased in a dose-related manner with a 54% decrease at 200 mg/kg. Enumeration of splenic subpopulations following GaAs (200 mg/kg) indicated a 58, 61, and 30% decrease in the total number of Thy 1.2 (T cells), Ig (B cells), and F4/80 (macrophages) positive cells, respectively, with no alterations in the percentages of these cells. Mitogenic responsiveness of splenocytes from GaAs-exposed mice was unaltered. To identify the splenic cell populations targeted by GaAs, the AFC response to SRBC was evaluated following cell separation/reconstitution of splenocytes from GaAs- (200 mg/kg, 24-hr exposure) and vehicle-exposed mice. Results demonstrated AFC suppression was due to functional alterations in both adherent (AD; macrophages) and nonadherent, (both T and B lymphocytes) cell populations. Further investigation focused on alterations in the AD population. Separation/reconstitution experiments demonstrated AFC suppression to SRBC was dependent on the concentration of macrophages from GaAs-exposed mice. This macrophage-mediated suppression of the in vitro AFC response could not be attributed to the presence of suppressor macrophages or release of prostaglandins.
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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/Arsenic,
http://linkedlifedata.com/resource/pubmed/chemical/Arsenicals,
http://linkedlifedata.com/resource/pubmed/chemical/Gallium,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M,
http://linkedlifedata.com/resource/pubmed/chemical/Mitogens,
http://linkedlifedata.com/resource/pubmed/chemical/gallium arsenide
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0041-008X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
110
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
129-42
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:1871769-Animals,
pubmed-meshheading:1871769-Antibody Formation,
pubmed-meshheading:1871769-Arsenic,
pubmed-meshheading:1871769-Arsenicals,
pubmed-meshheading:1871769-B-Lymphocytes,
pubmed-meshheading:1871769-Cell Separation,
pubmed-meshheading:1871769-Female,
pubmed-meshheading:1871769-Flow Cytometry,
pubmed-meshheading:1871769-Fluorescent Antibody Technique,
pubmed-meshheading:1871769-Gallium,
pubmed-meshheading:1871769-Immune Tolerance,
pubmed-meshheading:1871769-Immunoglobulin M,
pubmed-meshheading:1871769-Macrophages,
pubmed-meshheading:1871769-Mice,
pubmed-meshheading:1871769-Mitogens,
pubmed-meshheading:1871769-Spleen,
pubmed-meshheading:1871769-T-Lymphocytes,
pubmed-meshheading:1871769-Trachea
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pubmed:year |
1991
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pubmed:articleTitle |
Splenic cell targets in gallium arsenide-induced suppression of the primary antibody response.
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pubmed:affiliation |
Department of Pharmacology and Toxicology, Medical College of Virginia/Virginia Commonwealth University, Richmond 23298.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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