Bacterial Modulation of Human Fetal Membrane Toll-like Receptor Expression

被引:50
作者
Abrahams, Vikki M. [1 ]
Potter, Julie A. [1 ]
Bhat, Geeta [2 ]
Peltier, Morgan R. [3 ]
Saade, George [2 ]
Menon, Ramkumar [2 ]
机构
[1] Yale Univ, Sch Med, Dept Obstet Gynecol & Reprod Sci, New Haven, CT 06510 USA
[2] Univ Texas Med Branch, Dept Obstet & Gynecol, Galveston, TX 77555 USA
[3] Winthrop Univ Hosp, Dept Obstet & Gynecol, Mineola, NY 11501 USA
关键词
Bacteria; chorioamnion; infection; preterm birth; Toll-like receptor; NECROSIS-FACTOR-ALPHA; PORPHYROMONAS-GINGIVALIS LIPOPOLYSACCHARIDE; NF-KAPPA-B; PATTERN-RECOGNITION; CELL ACTIVATION; PRETERM LABOR; TNF-ALPHA; INFECTION; INFLAMMATION; APOPTOSIS;
D O I
10.1111/aji.12016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Problem Preterm premature rupture of fetal membranes (pPROM) occurs in 3040% 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 110 in fetal membranes after exposure to pathogens associated with intra-amniotic infection and PTB. 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 TLRs110. 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. 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.
引用
收藏
页码:33 / 40
页数:8
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