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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0017262,
umls-concept:C0024109,
umls-concept:C0024297,
umls-concept:C0024432,
umls-concept:C0026473,
umls-concept:C0034819,
umls-concept:C0036205,
umls-concept:C0085236,
umls-concept:C0086418,
umls-concept:C0087111,
umls-concept:C0205263,
umls-concept:C0205307,
umls-concept:C1171362,
umls-concept:C1515670
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pubmed:issue |
1
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pubmed:dateCreated |
1987-1-21
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pubmed:abstractText |
Expression of receptors for IL 2 was believed initially to be restricted to T cells after their activation by IL 1 and antigen. However, recently IL 2 receptors (IL 2R) were demonstrated on activated B cells by using an anti-IL 2R monoclonal antibody (anti-Tac). In this study, we examined the capacity of cultured human alveolar macrophages, blood monocytes, and myelomonocytic (HL-60) or monoblast (U937) cell lines to bind three different anti-IL 2R monoclonal antibodies before or after stimulation with the monocyte-activating agents IFN-gamma, LPS, phorbol ester, or lymphokine-containing conditioned medium. For each of the four cell populations examined, resting unstimulated cells bound little or no anti-IL 2R antibody, as shown independently by quantitative cell binding assay and by immunoperoxidase labeling. By contrast, incubation with recombinant IFN-gamma, conditioned medium, or to a lesser extent, native or recombinant IL 2 itself, resulted in a significant enhancement of anti-IL 2 receptor monoclonal antibody binding by all four populations, whereas LPS, PMA, or IL 1 had no effect. In addition, membrane binding of anti-Tac antibody, similar to that seen after stimulation of normal lung macrophages with IFN-gamma, was detected by using macrophages obtained by bronchoalveolar lavage of five patients with active pulmonary sarcoidosis. These findings are consistent with the expression of a functional IL 2R on activated cells of the monocyte lineage, since anti-Tac binding to IFN-gamma-treated HL-60 cells was inhibited by addition of excess IL-2; specific binding of anti-IL 2 monoclonal antibodies was detected in the presence of exogenous IL 2; and a 50 to 55 kD molecule was immunoprecipitated from both activated lung macrophages and T lymphoblasts by using anti-Tac antibody. We conclude that human mononuclear phagocytes can be induced by lymphokines to express IL 2R, and that such IL 2R+ macrophages can be detected in vivo during inflammation.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Lymphokines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2
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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 |
138
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
185-91
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:3097144-Cell Line,
pubmed-meshheading:3097144-Humans,
pubmed-meshheading:3097144-Interferon-gamma,
pubmed-meshheading:3097144-Interleukin-2,
pubmed-meshheading:3097144-Lung Diseases,
pubmed-meshheading:3097144-Lymphokines,
pubmed-meshheading:3097144-Macrophage Activation,
pubmed-meshheading:3097144-Macrophages,
pubmed-meshheading:3097144-Monocytes,
pubmed-meshheading:3097144-Pulmonary Alveoli,
pubmed-meshheading:3097144-Receptors, Immunologic,
pubmed-meshheading:3097144-Receptors, Interleukin-2,
pubmed-meshheading:3097144-Sarcoidosis
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pubmed:year |
1987
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pubmed:articleTitle |
Interleukin 2 receptors are expressed by alveolar macrophages during pulmonary sarcoidosis and are inducible by lymphokine treatment of normal human lung macrophages, blood monocytes, and monocyte cell lines.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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