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Bacterial modulation of human fetal membrane Toll-like receptor expression.

Authors :
Abrahams VM
Potter JA
Bhat G
Peltier MR
Saade G
Menon R
Source :
American journal of reproductive immunology (New York, N.Y. : 1989) [Am J Reprod Immunol] 2013 Jan; Vol. 69 (1), pp. 33-40. Date of Electronic Publication: 2012 Sep 11.
Publication Year :
2013

Abstract

Problem: Preterm premature rupture of fetal membranes (pPROM) occurs in 30-40% of spontaneous preterm births (PTB) and is associated with intra-amniotic infection and inflammation. The membranes may sense and respond to microbes via Toll-like receptors (TLRs); however, little is known about their expression and regulation in this tissue. The objective of this study was to evaluate the expression of TLRs 1-10 in fetal membranes after exposure to pathogens associated with intra-amniotic infection and PTB.<br />Method of Study: Normal human term fetal membrane explants were exposed to various bacteria. After 24 hrs, RNA was extracted and quantitative RT-PCR performed for TLRs1-10.<br />Results: Treatment of fetal membranes with Mycoplasma hominis increased expression of TLR4, TLR6, and TLR8 mRNA. Ureaplasma parvum upregulated TLR8 mRNA, and Porphyromonas gingivalis significantly increased fetal membrane TLR7 expression. In contrast, treatment with Gram-negative Escherichia coli (and its cell wall component lipopolysaccharide) downregulated TLR10 mRNA. No effect was detected for Ureaplasma urealyticum, Gardnerella vaginalis, or Group B Streptococcus.<br />Conclusion: These findings demonstrate that different types of bacteria have distinct effects on fetal membrane TLR expression patterns. Moreover, these findings highlight the disparity of fetal membrane responses to infection and thus suggest heterogeneity in the mechanisms by which infection-associated pregnancy complications, such as pPROM and PTB, arise.<br /> (© 2012 John Wiley & Sons A/S.)

Details

Language :
English
ISSN :
1600-0897
Volume :
69
Issue :
1
Database :
MEDLINE
Journal :
American journal of reproductive immunology (New York, N.Y. : 1989)
Publication Type :
Academic Journal
Accession number :
22967004
Full Text :
https://doi.org/10.1111/aji.12016