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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0007600,
umls-concept:C0014597,
umls-concept:C0021467,
umls-concept:C0021469,
umls-concept:C0021853,
umls-concept:C0041904,
umls-concept:C0071613,
umls-concept:C0086418,
umls-concept:C0162493,
umls-concept:C0441655,
umls-concept:C0806987,
umls-concept:C1292733,
umls-concept:C1550101,
umls-concept:C1948023
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pubmed:issue |
2
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pubmed:dateCreated |
1994-8-4
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pubmed:abstractText |
The polymeric IgR (pIgR) mediates transcytosis of polymeric IgA across mucosal epithelia. Expression of this receptor in HT-29.74 human colon carcinoma cells is up-regulated by the recombinant cytokines IFN-gamma, TNF-alpha, and IL-4. Here, we demonstrate that activation of freshly isolated human intestinal lamina propria mononuclear cells (LPMC) induces production of natural cytokines, and these act synergistically as potent stimulators of pIgR expression in HT-29.74 cells. LPMC from normal colonic mucosa were stimulated with PMA and calcium ionophore A-23187. The resulting supernatants consistently induced dose-dependent increases in pIgR expression by HT-29.74 cells, up to 65-fold. Analysis of four separate LPMC supernatants revealed mean concentrations of 8260 pg/ml for IFN-gamma, 420 pg/ml for TNF-alpha, and 15 pg/ml for IL-4. Ab-mediated neutralization of these cytokines suggested that the central regulator of pIgR expression in these supernatants was IFN-gamma. IL-4 neutralization had no effect on induction and TNF-alpha neutralization slightly reduced induction. In contrast, IFN-gamma neutralization abolished up to 93% of pIgR induction and had essentially the same effect as simultaneous neutralization of all three cytokines. In conclusion, our data demonstrate that natural cytokines, predominantly IFN-gamma, produced by stimulated human intestinal lymphocytes and macrophages have the capacity to up-regulate dramatically pIgR expression in an intestinal epithelial cell line, strongly suggesting that their action in vivo leads to enhancement of local defense functions mediated by IgA.
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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/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Secretory Component
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
153
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
675-81
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:8021503-Animals,
pubmed-meshheading:8021503-Cell Line,
pubmed-meshheading:8021503-Cytokines,
pubmed-meshheading:8021503-Humans,
pubmed-meshheading:8021503-Interferon-gamma,
pubmed-meshheading:8021503-Intestines,
pubmed-meshheading:8021503-Membrane Glycoproteins,
pubmed-meshheading:8021503-Mice,
pubmed-meshheading:8021503-Receptors, Immunologic,
pubmed-meshheading:8021503-Recombinant Proteins,
pubmed-meshheading:8021503-Secretory Component,
pubmed-meshheading:8021503-Up-Regulation
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pubmed:year |
1994
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pubmed:articleTitle |
Inhibition of IFN-gamma activity in supernatants from stimulated human intestinal mononuclear cells prevents up-regulation of the polymeric Ig receptor in an intestinal epithelial cell line.
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pubmed:affiliation |
Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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