Expression of chemokine decoy receptors and their ligands at the porcine maternal-fetal interface

被引:33
|
作者
Wessels, Jocelyn M. [2 ]
Linton, Nicola F. [2 ]
van den Heuvel, Marianne J. [2 ]
Cnossen, Sonya A. [2 ]
Edwards, Andrew K. [2 ]
Croy, Barbara Anne [1 ,2 ]
Tayade, Chandrakant [1 ,2 ]
机构
[1] Queens Univ, Dept Anat & Cell Biol, Kingston, ON K7L 3N6, Canada
[2] Univ Guelph, Ontario Vet Coll, Dept Biomed Sci, Guelph, ON N1G 2W1, Canada
来源
IMMUNOLOGY AND CELL BIOLOGY | 2011年 / 89卷 / 02期
基金
加拿大自然科学与工程研究理事会;
关键词
chemokines; decoy receptors; inflammation; reproductive immunology; trophoblast; uterus; DUFFY ANTIGEN RECEPTOR; RED-BLOOD-CELLS; INFLAMMATORY CYTOKINES; ENDOTHELIAL-CELLS; HUMAN ENDOMETRIUM; GENE-EXPRESSION; CUTTING EDGE; IN-VITRO; CCX-CKR; DARC;
D O I
10.1038/icb.2010.95
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Successful pregnancy requires coordinated maternal-fetal cross-talk to establish vascular connections that support conceptus growth. In pigs, two waves of spontaneous fetal loss occur and 30-40% of conceptuses are lost before parturition. Previous studies associated these losses with decreased angiogenic and increased inflammatory cytokines. Chemokines, a sub-category of cytokines, and decoy receptors control leukocyte trafficking, angiogenesis and development. The availability of chemokines is regulated by three non-signalling decoy receptors: chemokine decoy receptor (D6), Duffy antigen receptor for chemokines (DARC) and Chemocentryx decoy receptor (CCX CKR). We hypothesized that the expression of these receptors and their chemokine ligands regulate the porcine pregnancy success or failure. Here, we describe for the first time the transcription and translation of all three decoy receptors and several chemokine ligands in endometrium and trophoblast associated with healthy and arresting conceptuses at gestation day (gd) 20 and gd50. Among decoy receptors, transcripts for DARC were significantly reduced in endometrium, whereas that for CCX CKR were significantly increased in endometrium and trophoblast at gd50 arresting compared with healthy sites. However, western blot analysis revealed no differences in decoy receptor expression between healthy and arresting tissues. Transcripts for decoy receptor ligands CCL2, CCL3, CCL4, CCL5, CCL11, CCL19, CCL21, CXCL2 and CXCL8 were stable between healthy and arresting littermates. Quantification by SearchLight chemiluminescent protein array confirmed ligand expression at the protein level. These data indicate that decoy receptors and ligands are expressed at the porcine maternal-fetal interface and dysregulation of decoy receptor (DARC and CCX CKR) transcripts occurs at sites of fetal arrest. Immunology and Cell Biology (2011) 89, 304-313; doi:10.1038/icb.2010.95; published online 3 August 2010
引用
收藏
页码:304 / 313
页数:10
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