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Bacterial DNA evokes epithelial IL‐8 production by a MAPK‐dependent, NFκB‐independent pathway
Author(s) -
Akhtar Mahmood,
Watson James L.,
Nazli Aisha,
McKay Derek M.
Publication year - 2003
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.02-0950fje
Subject(s) - nf κb , mapk/erk pathway , microbiology and biotechnology , chemistry , signal transduction , biology
Recognition of bacterial products by the innate immune system is dependent on pattern‐recognition receptors: toll‐like receptor 9 (TLR‐9) in the case of bacterial DNA. We hypothesized that bacterial DNA can directly affect enteric epithelial cells. RT‐PCR revealed constitutive TLR‐9 mRNA expression in three human colonic epithelial cell lines (T84, HT‐29, Caco‐2) and THP‐1 monocytes. Epithelial cells, in six‐well culture plates or on filter supports, were exposed to E. coli DNA (1–50 µg/ml), synthetic CpG‐rich oligonucleotides, or calf thymus DNA for 6–48 h. Exposure to E. coli DNA resulted in an increase in IL‐8 mRNA, and a time‐and dose‐dependent increase in IL‐8 secretion. Also, CpG oligonucleotides induced epithelial IL‐8 production, whereas calf thymus DNA did not. Exposure to E. coli DNA resulted in phosphorylation of ERK 1/2 MAPK and inhibitors of ERK activity (PD98059, UO126) significantly reduced the evoked IL‐8 production. In contrast, inhibitors of NFκB activity (PDTC, SN50) did not block E. coli DNA‐induced IL‐8 production. Electrophoretic mobility shift assays revealed that E. coli DNA stimulated epithelial AP‐1 but not NFκB activation. The barrier (i.e., transepithelial resistance) and ion transport parameters of epithelial monolayers (assessed in Ussing chambers) were unaltered following E. coli DNA exposure. Thus model gut epithelia express TLR‐9 mRNA and, while maintaining their barrier function, can respond to E. coli DNA by increased IL‐8 production.