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The Role of Toll-Like Receptors (TLR-2 and -4) and Triggering Receptor Expressed on Myeloid Cells 1 (TREM-1) in Human Term and Preterm LaborNinewells Hospital and School of Medicine, Dundee, United Kingdom, ryoussef{at}nhs.net
The Queen Mother's Hospital, Yorkhill, Glasgow, United Kingdom
Reproductive & Maternal Medicine, University of Glasgow, Third Floor, Queen Elizabeth Building, Glasgow Royal Infirmary, United Kingdom
Reproductive & Maternal Medicine, University of Glasgow, Third Floor, Queen Elizabeth Building, Glasgow Royal Infirmary, United Kingdom
Reproductive & Maternal Medicine, University of Glasgow, Third Floor, Queen Elizabeth Building, Glasgow Royal Infirmary, United Kingdom
Reproductive & Maternal Medicine, University of Glasgow, Third Floor, Queen Elizabeth Building, Glasgow Royal Infirmary, United Kingdom
University of Edinburgh Centre for Reproductive Biology, The Queen's Medical Research Institute, Edinburgh, United Kingdom Objective. To define the role of Toll-like receptors (TLR-2, TLR-4) and triggering receptor expressed on myeloid cells-1 (TREM-1) in pregnant human myometrium. Study Design. Expression of TLR-2 and -4 mRNA and protein and TREM-1 mRNA was quantified in human myometrial samples. Subsequently, we investigated the effect of medroxyprogesterone acetate (MPA) as a functional inhibitor of the TLR agonist lipopolysaccharide (LPS). Results. Messenger RNA expression of TLR-2 and -4 was significantly higher in myometrium at term compared with preterm (P = .009 and .016, respectively). Toll-like receptor-2 protein expression was significantly higher during labor (P = .002) compared with nonlaboring samples. Triggering receptor expressed on myeloid cells-1 mRNA expression was increased in both myometrium and cervix after labor at term (P < .05). Medroxyprogesterone acetate significantly suppressed LPS-induced production of interleukin 1b (IL-1b), IL-6, and IL-8 in vitro (P < .05). Conclusion. Toll-like receptors 2and 4 and TREM-1 are expressed in human myometrium and may play a role in the mechanism of labor at term, and their functional effects are inhibited by MPA.
Key Words: Inflammation mechanism of human parturition.
This version was published on September
1, 2009 Reproductive Sciences, Vol. 16, No. 9,
843-856 (2009) |
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