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Volume 84, Issue 1, Pages 41-51 (January 2010)


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Expression and function of Toll-like receptors in human endometrial epithelial cell lines

Wedad Aboussahouda, Reza Aflatooniana1, Chris Brucea, Sarah Elliotta, Jon Wardb, Sue Newtonc, Sabine Hombach-Klonischd, Thomas Klonischd, Alireza FazeliaCorresponding Author Informationemail address

Received 26 July 2009; received in revised form 9 September 2009; accepted 10 September 2009. published online 18 November 2009.

Abstract 

In mammals, Toll-like receptors (TLRs) are the principal family of innate immune pattern recognition receptors (PRRs). The main function for TLRs is the detection of molecular patterns associated with invading pathogens. We investigated TLR expression and function in three established human endometrial epithelial cell lines, including hTERT-EEC, HEC-1B and Ishikawa cells, and clarified the application of these endometrial cell lines as in vitro models for studying TLR expression and function in the female reproductive tract. TLR gene expression was examined by RT-PCR and protein localization by immunohistochemistry. Our results showed that TLR expression in these cell lines is comparable to published literature on TLR expression in primary human endometrial tissue. TLR function was investigated by the detection of IL-6 and IL-8 production by ELISA in response to TLR2, TLR3, TLR5, TLR7 and TLR9 ligands. We found that hTERT-EEC cells were responsive to TLR5 ligand and HEC-1B cells respond to TLR3 and TLR5 ligands. In contrast, Ishikawa cells respond only to PMA/I which was used as a positive control for IL-8 production. Finally, we investigated the influence of flagellin as a TLR5 stimulant on TLR5 expression in these cell lines by QPCR. Our results showed that the endometrial cell lines showed a tendency for increased TLR5 expression in response to flagellin stimulation and in hTERT-EEC cells this tendency was statistically significant. These results suggest that hTERT-EEC, HEC-1B and Ishikawa cell lines can be used as in vitro models to investigate innate immune responses of endometrial cells in the female reproductive tract.

a Academic Unit of Reproductive and Developmental Medicine, The University of Sheffield, Level 4, Jessop Wing, Tree Root Walk, Sheffield S10 2SF, UK

b Cardiovascular Research Unit, Royal Hallamshire Hospital, Glossop Road, University of Sheffield, Sheffield S10 2JF, UK

c Medical School, University of Sheffield Beech Hill Road, Sheffield S10 2RX, UK

d Department Human Anatomy and Cell Science, Faculty of Medicine, University of Manitoba, Winnipeg R3E 0J9, Canada

Corresponding Author InformationCorresponding author. Tel.: +44 114 2268195.

1 Present address: Reproductive and Biomedicine Group, Medical School, Iran University of Medical Sciences, Tehran 14155-5983, Iran.

PII: S0165-0378(09)00499-9

doi:10.1016/j.jri.2009.09.008


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