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Parasitol Int ; 59(4): 616-21, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20887801

ABSTRACT

Biliary tract infection with the Group I carcinogenic liver fluke Opisthorchis viverrini is associated with severe inflammation leading to cholangiocarcinoma--a major biliary cancer in Southeast Asia. However, mechanism(s) by which the liver fluke induces host mucosal immune/inflammatory responses is unclear. In the present study we address whether a normal immortalized human cholangiocyte cell line (H69 cells) recognizes and responds to O. viverrini excretory/secretory products (OVES). Expression of multiple TLRs, activation of NF-κB, and expression of pro-inflammatory cytokines were monitored in the presence and absence of OVES. Our results showed that OVES induced increased cholangiocyte TLR4 mRNA expression, induced IκB-α degradation in a MyD88-dependent manner, and activated NF-κB nuclear translocation. Moreover, OVES induced expression and secretion of the strong chemoattractant chemokine interleukin 8 (IL-8) and pro-inflammatory cytokine IL-6. These results demonstrate that secreted/excreted products of O. viverrini are recognized by human cholangiocytes and initiate innate mucosal immunity/inflammatory cascades, a primary event in the pathogenesis of opisthorchiasis and cholangiocarcinoma.


Subject(s)
Bile Ducts/immunology , Helminth Proteins/immunology , Interleukin-6/metabolism , Interleukin-8/metabolism , Opisthorchis/immunology , Toll-Like Receptor 4/metabolism , Animals , Bile Ducts/cytology , Cell Line, Transformed , Cholangiocarcinoma/immunology , Cholangiocarcinoma/physiopathology , Cricetinae , Epithelial Cells/immunology , Helminth Proteins/genetics , Helminth Proteins/metabolism , Humans , Interleukin-6/genetics , Interleukin-8/genetics , Male , Mesocricetus , Myeloid Differentiation Factor 88/genetics , Myeloid Differentiation Factor 88/metabolism , NF-kappa B/genetics , NF-kappa B/metabolism , Opisthorchiasis/immunology , Opisthorchiasis/physiopathology , Opisthorchis/metabolism , Opisthorchis/pathogenicity , Toll-Like Receptor 4/genetics , Up-Regulation
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