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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1986-12-15
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pubmed:abstractText |
DMN exposure modulates cellular immunity through alterations in the maturation and hematopoiesis of macrophages. DMN-exposed bone marrow stem cells gave rise to increased colony-forming unit-macrophage (CFU-M) colonies while the resulting colonies produced fewer cells/colony. Bone marrow-derived macrophages phenotypically had decreased cells expressing Ia antigens or cells in the S-phase following DMN treatment. Concanavalin A-elicited peritoneal exudate cells from DMN-treated animals demonstrated an increase in the percentage of macrophages and in the number of immature, bi-nucleated cells obtained as well as a concomitant increase in the percentage of Ia antigen-expressing cells. Concanavalin A-elicited peritoneal exudate cells from DMN-exposed animals also had an increased secreted interleukin-1 activity following lipopolysaccharide stimulation without any alteration in the expression of membrane-bound interleukin-1. Thioglycolate-elicited peritoneal exudate cells from DMN-exposed animals demonstrated no changes in cellularity and only showed increases in the percentage of bi-nucleated cells. There were no alterations in the capacity of T cells obtained from DMN-treated animals to respond to either soluble (keyhole limpet hemocyanin) or allo-antigens; nor were there alterations in the capacity of these T cells to either produce or respond to interleukin-2. These findings suggest that the observed DMN-induced modulation(s) in cell-mediated immunity results from changes in macrophage hematopoiesis due to alterations in: the production of regulatory factors controlling their production and/or differentiation or their ability to respond to these factors.
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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/Dimethylnitrosamine,
http://linkedlifedata.com/resource/pubmed/chemical/Histocompatibility Antigens Class II,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-3
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0162-3109
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
105-15
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:3490456-Animals,
pubmed-meshheading:3490456-Antigen-Presenting Cells,
pubmed-meshheading:3490456-Cell Differentiation,
pubmed-meshheading:3490456-Dimethylnitrosamine,
pubmed-meshheading:3490456-Female,
pubmed-meshheading:3490456-Hematopoietic Stem Cells,
pubmed-meshheading:3490456-Histocompatibility Antigens Class II,
pubmed-meshheading:3490456-Immunity, Cellular,
pubmed-meshheading:3490456-Interleukin-1,
pubmed-meshheading:3490456-Interleukin-2,
pubmed-meshheading:3490456-Interleukin-3,
pubmed-meshheading:3490456-Macrophages,
pubmed-meshheading:3490456-Mice,
pubmed-meshheading:3490456-Mice, Inbred C3H,
pubmed-meshheading:3490456-Mice, Inbred C57BL,
pubmed-meshheading:3490456-T-Lymphocytes
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pubmed:year |
1986
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pubmed:articleTitle |
Alteration of macrophage differentiation into accessory and effector cells from exposure to dimethylnitrosamine (DMN) in vivo.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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