Source:http://linkedlifedata.com/resource/pubmed/id/12707335
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2003-4-22
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pubmed:abstractText |
We have previously reported that FcgammaR-mediated function in myeloid cells is a tightly regulated event that is influenced by the cytokines present in the milieu. TGF-beta1 is an immunosuppressive cytokine with pleiotropic effects on immune responses; however, the molecular mechanism by which TGF-beta suppresses immune responses is poorly understood. In this study, we have analyzed the effect of TGF-beta on FcgammaR-mediated activation of myeloid cells. We report that TGF-beta1-treated THP-1 human myeloid cells displayed reduced ability to phagocytose IgG-coated particles. Because FcgammaR expression is modulated by cytokines, we analyzed expression levels of FcgammaRI, FcgammaRIIa, FcgammaRIIb, and FcgammaRIIIa in cells cultured with or without TGF-beta1 and found while total protein levels of the FcgammaR were not reduced, surface expression of FcgammaRI and FcgammaRIII was lower in cells cultured with TGF-beta1. Concomitantly, there was a dose-dependent reduction in the expression of the FcgammaR-associated gamma-subunit. This suppressive effect of TGF-beta was likewise observed in bone marrow-derived murine myeloid cells and human monocytes. Importantly, TGF-beta1 also significantly reduced the production of monocyte chemoattractant protein-1 induced by immobilized IgG, which would further reduce monocyte recruitment to the site of inflammation. In contrast, human alveolar macrophages were refractory to this effect, expressing low levels of TGF-beta type II receptors compared with peripheral blood monocytes from the same donor. These data provide insight into the regulation of immune responses by TGF-beta1 and demonstrate the selectivity of these effects.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/P01 CA095426,
http://linkedlifedata.com/resource/pubmed/grant/P01 HL70294,
http://linkedlifedata.com/resource/pubmed/grant/P30 CA16058,
http://linkedlifedata.com/resource/pubmed/grant/R01 HL 66108,
http://linkedlifedata.com/resource/pubmed/grant/R01 HL63800
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chemokine CCL2,
http://linkedlifedata.com/resource/pubmed/chemical/IL2RG protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Il2rg protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin Receptor Common gamma...,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Subunits,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, IgG,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-7,
http://linkedlifedata.com/resource/pubmed/chemical/TGFB1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Tgfb1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta1
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pubmed:status |
MEDLINE
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pubmed:month |
May
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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 |
170
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4572-7
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:12707335-Animals,
pubmed-meshheading:12707335-Cell Line, Transformed,
pubmed-meshheading:12707335-Chemokine CCL2,
pubmed-meshheading:12707335-Down-Regulation,
pubmed-meshheading:12707335-Humans,
pubmed-meshheading:12707335-Interleukin Receptor Common gamma Subunit,
pubmed-meshheading:12707335-Macrophages, Alveolar,
pubmed-meshheading:12707335-Mice,
pubmed-meshheading:12707335-Monocytes,
pubmed-meshheading:12707335-Myeloid Cells,
pubmed-meshheading:12707335-Phagocytosis,
pubmed-meshheading:12707335-Protein Subunits,
pubmed-meshheading:12707335-Receptors, IgG,
pubmed-meshheading:12707335-Receptors, Interleukin-7,
pubmed-meshheading:12707335-Signal Transduction,
pubmed-meshheading:12707335-Transforming Growth Factor beta,
pubmed-meshheading:12707335-Transforming Growth Factor beta1,
pubmed-meshheading:12707335-Tumor Cells, Cultured
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pubmed:year |
2003
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pubmed:articleTitle |
TGF-beta 1 suppresses [correction of supresses] myeloid Fc gamma receptor function by regulating the expression and function of the common gamma-subunit.
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pubmed:affiliation |
Department of Internal Medicine and Dorothy M. Davis Heart and Lung Research Institute, and The James Cancer Hospital and Comprehensive Cancer Center, Ohio State University, Columbus, OH 43210, USA. tridandapani.2@osu.edu
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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