Fetal membranes exhibit selective leukocyte chemotaxic activity during human labor

被引:113
作者
Gomez-Lopez, N. [1 ,2 ]
Estrada-Gutierrez, G. [1 ]
Jimenez-Zamudio, L. [2 ]
Vega-Sanchez, R. [1 ]
Vadillo-Ortega, R. [1 ]
机构
[1] Inst Nacl Perinatol Isidro Espinosa de los Reyes, Res Direct, Mexico City 11000, DF, Mexico
[2] Inst Politecn Nacl, Escuela Nacl Ciencias Biol, Dept Immunol, Mexico City 11340, DF, Mexico
关键词
Fetal membranes; Chemotaxis; Human labor; HUMAN ENDOMETRIUM; PREGNANCY DECIDUA; HUMAN PARTURITION; CELL-POPULATIONS; T-CELLS; EXPRESSION; CHEMOKINE; TERM; INTERLEUKIN-8; MYOMETRIUM;
D O I
10.1016/j.jri.2009.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
One of the characteristics of the labor process in women is leukocyte recruitment into reproductive tissues. These migrating cells may play a role in the induction of functional and biochemical changes associated with the rupture of fetal membranes during labor. This study was undertaken to assess whether human fetal membranes induce leukocyte chemotaxis during labor as well as to identify and characterize leukocyte chemoattractants secreted by these tissues. Leukocyte chemotactic activity of fetal membrane extracts obtained from women with full-term pregnancies and spontaneous active labor was compared with extracts from women without labor. The number and phenotype of attracted leukocytes were analyzed by flow cytometry. Chemokines were quantified using a Multiplex system and were identified by immunofluorescence histochemistry. Although all tested extracts induced chemotaxis of leukocytes, those prepared from women undergoing labor induced higher responses. Polymorphonuclear leukocyte chemotaxis increased approximately three-fold in response to extract from fetal membranes with labor. The same extracts elicited a significant increase in attracted monocytes (36-fold) as well as T and B lymphocytes, and NK cells (all five-fold) when compared to extracts from women without labor. This enhanced chemotactic activity was associated with the presence of IL-8, MCP-1, UP-10 and MIP-1 alpha. We conclude that fetal membrane extracts obtained from women during labor exhibit selective chemotaxis for specific leukocyte subpopulations in vitro. This process may contribute to a microenvironment composed of specific leukocytes that promotes and amplifies biochemical changes in the fetal membranes during labor. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:122 / 131
页数:10
相关论文
共 41 条
[21]  
Kelly R W, 1996, Rev Reprod, V1, P89, DOI 10.1530/revreprod/1.2.89
[22]   Spatial and temporal expression of ligands for CXCR3 and CXCR4 in human endometrium [J].
Kitaya, K ;
Nakayama, T ;
Daikoku, N ;
Fushiki, S ;
Honjo, H .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2470-2476
[23]   Human neutrophil collagenase (matrix metalloproteinase 8) in parturition, premature rupture of the membranes, and intrauterine infection [J].
Maymon, E ;
Romero, R ;
Pacora, P ;
Gomez, R ;
Athayde, N ;
Edwin, S ;
Yoon, BH .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2000, 183 (01) :94-99
[24]   PROGESTERONE SYNTHESIS BY HUMAN AMNION, CHORION, AND DECIDUA AT TERM [J].
MITCHELL, BF ;
CHALLIS, JRG ;
LUKASH, L .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1987, 157 (02) :349-353
[25]  
OKSENBERG JR, 1988, AM J REPROD IMMUNOL, V164, P151
[26]   Leukocyte density and pro-inflammatory cytokine expression in human fetal membranes, decidua, cervix and myometrium before and during labour at term [J].
Osman, I ;
Young, A ;
Ledingham, MA ;
Thomson, AJ ;
Jordan, F ;
Greer, IA ;
Norman, JE .
MOLECULAR HUMAN REPRODUCTION, 2003, 9 (01) :41-45
[27]   ORIGIN OF CERVICAL COLLAGENASE DURING PARTURITION [J].
OSMERS, R ;
RATH, W ;
ADELMANNGRILL, BC ;
FITTKOW, C ;
KULOCZIK, M ;
SZEVERENYI, M ;
TSCHESCHE, H ;
KUHN, W .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 166 (05) :1455-1460
[28]   INTERLEUKIN-8 SYNTHESIS AND THE ONSET OF LABOR [J].
OSMERS, RGW ;
BLASER, J ;
KUHN, W ;
TSCHESCHE, H .
OBSTETRICS AND GYNECOLOGY, 1995, 86 (02) :223-229
[29]   A NOVEL NEUTROPHIL-ACTIVATING FACTOR PRODUCED BY HUMAN MONONUCLEAR PHAGOCYTES [J].
PEVERI, P ;
WALZ, A ;
DEWALD, B ;
BAGGIOLINI, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (05) :1547-1559
[30]   INFECTION AND PRETERM LABOR [J].
ROMERO, R ;
MAZOR, M .
CLINICAL OBSTETRICS AND GYNECOLOGY, 1988, 31 (03) :553-584