Expression of Coagulation-Related Protein Genes During LPS-Induced Preterm Delivery in the Pregnant Mouse

被引:9
|
作者
Phillippe, Mark [1 ]
Diamond, Allaire K. [1 ]
Sweet, Leigh M. [1 ]
Oppenheimer, Karen H. [1 ]
Bradley, Diana F. [1 ]
机构
[1] Univ Vermont, Coll Med, Dept Obstet Gynecol & Reprod Sci, Burlington, VT 05405 USA
关键词
plasminogen activator inhibitor 1; tissue factor; lipopolysaccharide; preterm delivery; CD-1; mouse; PLASMINOGEN-ACTIVATOR INHIBITOR-1; EXPERIMENTAL ENDOTOXEMIA; INTRAUTERINE INFECTION; TISSUE FACTOR; LIPOPOLYSACCHARIDE; INFLAMMATION; CYTOKINES; BIRTH; MICE; FIBRINOLYSIS;
D O I
10.1177/1933719111404607
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Preterm delivery (PTD) has been associated with inflammation along with activation of the coagulation pathway. These studies sought to characterize the expression of several coagulation pathway genes including plasminogen activator inhibitor 1 (PAI-1), tissue factor (TF), protease-activated receptor 1 (Par1), protease-activated receptor 2 (Par2), fibrinogen-like protein 2 (Fgl2), and thrombomodulin (TM) during lipopolysaccharide (LPS)-induced PTD in day 15 pregnant CD-1 mice. Western blot studies confirmed protein expression for PAI-1, Par1, Par2, Fgl2, and TM in the mouse uterus. Quantitative reverse transcriptase polymerase chain reaction (RT-PCR) confirmed increased PAI-1 messenger RNA (mRNA) in the uteri, lung, kidney, and liver tissues at 2 to 6 hours after LPS injection. In contrast, TF expression significantly decreased by 12 hours in uterine tissue; whereas, its expression was unchanged in the other maternal tissues. The uterine mRNA for Par1, Par2, Fgl2, and TM remained stable. In summary, these studies have confirmed expression of coagulation pathway genes within the pregnant uterus; some of which are modulated during LPS-induced PTD.
引用
收藏
页码:1071 / 1079
页数:9
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