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Filaggrin knockdown and Toll‐like receptor 3 (TLR3) stimulation enhanced the production of thymic stromal lymphopoietin (TSLP) from epidermal layers
Author(s) -
Lee Kyung Ho,
Cho KyungAh,
Kim JiYoon,
Kim JinYoung,
Baek JiHae,
Woo SoYoun,
Kim JinWoo
Publication year - 2011
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/j.1600-0625.2010.01203.x
Subject(s) - thymic stromal lymphopoietin , filaggrin , immunology , toll like receptor , hacat , immune system , microbiology and biotechnology , tlr7 , innate immune system , biology , tlr3 , atopic dermatitis , cell culture , genetics
Keratinocytes constitute the first‐line barrier against exogenous antigens and contain Toll‐like receptors (TLRs), which function as pattern‐recognition molecules to activate antimicrobial innate immune responses. In an effort to ascertain whether or not filaggrin ( fil ament‐ aggr egating prote in ) expression affected the TLR‐mediated responses of keratinocytes, we transfected filaggrin siRNA into HaCaT human keratinocyte cells and determined that thymic stromal lymphopoietin (TSLP) and IL‐6 secretion were increased by poly(I:C) stimulus. Additionally, TSLP expression is increased in filaggrin knockdown as well as TLR3 stimulation in reconstituted human epidermal layers. Therefore, the findings of this study show that reduced filaggrin levels may influence innate immune responses via TLR stimuli and may contribute to the pathogenesis of inflammatory skin disease via TSLP expression.
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