Source:http://linkedlifedata.com/resource/pubmed/id/16424222
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2006-1-20
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pubmed:abstractText |
Keratinocytes contribute to cutaneous immune responses through the expression of cytokines. We investigated whether human keratinocytes can express IL-23, a newly defined IFN-gamma-inducing cytokine composed of a unique p19 subunit and a p40 subunit shared with IL-12. Cultured keratinocytes from normal and lesional psoriatic skin were found to express constitutively mRNA for both subunits of IL-23. Low but significant levels of the heterodimeric IL-23 protein could be detected in cell lysates and supernatants from stimulated keratinocytes by immunoblotting and ELISA. Functional analysis showed that these low levels of keratinocyte-derived IL-23 were sufficient to enhance the IFN-gamma production by memory T cells. Immunostaining of skin sections confirmed expression of both subunits of IL-23 by keratinocytes in situ and also revealed expression of this cytokine in the dermal compartment. IL-23 expression was significantly higher in psoriatic lesional skin, compared with normal and psoriatic nonlesional skin. The immunostained preparations of cultured cells and IL-23 levels in culture supernatants did not show any difference between normal and psoriatic keratinocytes indicating no intrinsic aberration of IL-23 expression in keratinocytes from psoriatic skin. Double staining of cytospin preparations demonstrated that IL-23 p19 is also expressed by epidermal Langerhans cells, dermal dendritic cells, and macrophages. Psoriasis is a chronic inflammatory skin disease mediated by IFN-gamma-expressing type 1 memory T cells. As IL-23 is important to activate memory T cells to produce IFN-gamma, its augmented expression of IL-23 by keratinocytes and cutaneous APC may contribute to the perpetuation of the inflammation process in this disease.
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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/Adjuvants, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/IL23A protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Inflammation Mediators,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-23,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-23 Subunit p19,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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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 |
176
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1908-15
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16424222-Adjuvants, Immunologic,
pubmed-meshheading:16424222-Antigen-Presenting Cells,
pubmed-meshheading:16424222-Cells, Cultured,
pubmed-meshheading:16424222-Dermis,
pubmed-meshheading:16424222-Dimerization,
pubmed-meshheading:16424222-Epidermis,
pubmed-meshheading:16424222-Humans,
pubmed-meshheading:16424222-Immunologic Memory,
pubmed-meshheading:16424222-Inflammation Mediators,
pubmed-meshheading:16424222-Interferon-gamma,
pubmed-meshheading:16424222-Interleukin-23,
pubmed-meshheading:16424222-Interleukin-23 Subunit p19,
pubmed-meshheading:16424222-Interleukins,
pubmed-meshheading:16424222-Keratinocytes,
pubmed-meshheading:16424222-Psoriasis,
pubmed-meshheading:16424222-RNA, Messenger,
pubmed-meshheading:16424222-Skin,
pubmed-meshheading:16424222-T-Lymphocytes
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pubmed:year |
2006
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pubmed:articleTitle |
In vitro and in situ expression of IL-23 by keratinocytes in healthy skin and psoriasis lesions: enhanced expression in psoriatic skin.
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pubmed:affiliation |
Department of Dermatology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands. g.piskin@amc.uva.nl
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pubmed:publicationType |
Journal Article
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