Stress increases VCAM-1 expression at the fetomaternal interface in an abortion-prone mouse model

被引:15
|
作者
Prados, M. B. [1 ]
Solano, M. E. [2 ]
Friebe, A. [3 ,4 ]
Blois, S. [5 ]
Arck, P. [2 ]
Miranda, S. [1 ]
机构
[1] Univ Buenos Aires, CONICET, GlycoImmunoBiol Lab, Inst Invest Cardiol Prof Dr Alberto C Taquini INI, Buenos Aires, DF, Argentina
[2] Univ Hosp Hamburg Eppendorf, Lab Fetomaternal Med, Dept Obstet & Fetal Med, Hamburg, Germany
[3] Univ Med Berlin, Charite, Berlin, Germany
[4] Ruhr Univ Bochum, Dept Psychiat, Bochum, Germany
[5] Univ Med Berlin, Charite Ctr Innere Med & Dermatol 12, Reprod Immunol Res Grp, Berlin, Germany
关键词
Adhesion molecules; Inflammation; PECAM; Pregnancy; Vessels; BOOSTED SPONTANEOUS-ABORTION; CELL-ADHESION MOLECULE-1; PROCOAGULANT FGL2; PREGNANCY; MICE; SUCCESS; ACTIVATION; MECHANISM; FAILURE; ECOLOGY;
D O I
10.1016/j.jri.2011.01.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sound stress exposure increases fetal loss via inflammatory pathways. Inflammation is known to up-regulate cell adhesion molecules, such as vascular cell adhesion molecule-1 (VCAM-1), which mediates the adhesion of leukocytes to the vascular endothelium. In this work, we studied the frequency of VCAM-1(+) vessels at the fetomaternal interface in stressed and non-stressed pregnant CBA/J female mice mated with DBA/2J (high fetal loss model) or BALB/c (low fetal loss model) males. The high fetal loss model had fewer large vessels on gestation day 6.5. and stress reduced the frequency of large vessels to a similar number in both high and low fetal loss models. In the high fetal loss model, however, the frequency of VCAM-1+ vessels was dramatically increased. This study shows that VCAM-1 expression is modulated by stress at the fetomaternal interface in abortion-prone cross-breeding. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:207 / 211
页数:5
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