Feto-maternal interactions in pregnancies: Placental microparticles activate peripheral blood monocytes

被引:112
作者
Messerli, M. [1 ]
May, K. [2 ,3 ]
Hansson, S. R. [2 ]
Schneider, H. [4 ]
Holzgreve, W. [1 ]
Hahn, S. [1 ]
Rusterholz, C. [1 ]
机构
[1] Univ Basel Hosp, Dept Biomed, Lab Prenatal Med, CH-4031 Basel, Switzerland
[2] Lund Univ, Univ Lund Hosp, Dept Obstet & Gynecol, Lund, Sweden
[3] Univ Greifswald, Dept Clin Pharmacol, D-17487 Greifswald, Germany
[4] Univ Bern, Dept Obstet & Gynecol, CH-3000 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
Pregnancy; Placental microparticles; Monocytes; Feto-maternal interactions; SYNCYTIOTROPHOBLAST MICROVILLOUS MEMBRANES; NF-KAPPA-B; PREECLAMPTIC WOMEN; ENDOTHELIAL-CELLS; APOPTOSIS; CYTOKINES; INFLAMMATION; TROPHOBLAST; CIRCULATION; IMMUNITY;
D O I
10.1016/j.placenta.2009.11.011
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Normal pregnancy is associated with a systemic maternal inflammatory reaction, including the activation of peripheral blood monocytes. This reaction is exaggerated in pre-eclampsia, a severe placenta-dependent disorder of pregnancy specific to humans It has been suggested that placental syncytiotrophoblast membrane microparticles (STBM), which are released into the peripheral blood, may contribute to the maternal response The aim of this study was to investigate the inflammatory properties of STBM generated by four different approaches on primary human monocytes in vitro. Cellular viability, phenotype and functional response were analysed STBM isolated by mechanical dissection and STBM generated from villous explant Cultures incubated in hypoxic conditions had only minor influences on the monocytic phenotype and failed to induce a proinflammatory response By contrast, STBM washed from the maternal side of a placental cotyledon and STBM shed by explants cultured in air up-regulated cell surface expression of the adhesion molecule CD54 and induced the production of interleukin (IL)-8, IL-6 and IL-1 beta. Cytokine production was time- and dose-dependent. Our study, therefore, suggests that monocyte activation in normal pregnancy and pre-eclampsia may be induced by STBM released by the placenta. The higher amounts of STBM circulating in maternal blood in pre-eclampsia might lead to the excessive maternal inflammatory reaction. (C) 2009 Elsevier Ltd All rights reserved
引用
收藏
页码:106 / 112
页数:7
相关论文
共 44 条
[1]   The effects of apoptotic, deported human placental trophoblast on macrophages: Possible consequences for pregnancy [J].
Abumaree, M. H. ;
Stone, P. R. ;
Chamley, L. W. .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2006, 72 (1-2) :33-45
[2]   Neutrophils are stimulated by syncytiotrophoblast microvillous membranes to generate superoxide radicals in women with preeclampsia [J].
Aly, AS ;
Khandelwal, M ;
Zhao, J ;
Mehmet, AH ;
Sammel, MD ;
Parry, S .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2004, 190 (01) :252-258
[3]   Nuclear factor-κB, p38, and stress-activated protein kinase mitogen-activated protein kinase signaling pathways regulate proinflammatory cytokines and apoptosis in human placental explants in response to oxidative stress -: Effects of antioxidant vitamins [J].
Cindrova-Davies, Tereza ;
Spasic-Boskovic, Olivera ;
Jauniaux, Eric ;
Charnock-Jones, D. Stephen ;
Burton, Graham J. .
AMERICAN JOURNAL OF PATHOLOGY, 2007, 170 (05) :1511-1520
[4]   Human placental syncytiotrophoblast microvillous membranes impair maternal vascular endothelial function [J].
Cockell, AP ;
Learmont, JG ;
Smarason, AK ;
Redman, CWG ;
Sargent, IL ;
Poston, L .
BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY, 1997, 104 (02) :235-240
[5]  
Conrad KP, 1998, AM J REPROD IMMUNOL, V40, P102
[6]   Dual in vitro perfusion of an isolated cotyledon as a model to study the implication of changes in the third trimester placenta on preeclampsia [J].
Di Santo, S. ;
Sager, R. ;
Andres, A.-C. ;
Guller, S. ;
Schneider, H. .
PLACENTA, 2007, 28 :S23-S32
[7]   Plasma of pregnant and preeclamptic women activates monocytes in vitro [J].
Faas, M. M. ;
Donker, R. B. ;
van Pampus, M. G. ;
Huls, A. M. F. ;
Salomons, J. ;
de Vos, P. ;
Aarnoudse, J. G. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2008, 199 (01) :84.e1-84.e8
[8]   Interleukin-18 and interleukin-1β:: Two cytokine substrates for ICE (Caspase-1) [J].
Fantuzzi, G ;
Dinarello, CA .
JOURNAL OF CLINICAL IMMUNOLOGY, 1999, 19 (01) :1-11
[9]  
Garcia-Lloret MI, 2000, J LEUKOCYTE BIOL, V68, P903
[10]   Systemic inflammatory priming in normal pregnancy and preeclampsia: The role of circulating syncytiotrophoblast microparticles [J].
Germain, Sarah J. ;
Sacks, Gavin P. ;
Soorana, Suren R. ;
Sargent, Ian L. ;
Redman, Christopher W. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (09) :5949-5956