Source:http://linkedlifedata.com/resource/pubmed/id/16816146
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2006-8-30
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pubmed:abstractText |
Remodeling of uterine spiral arteries is critical for the continuation of a successful pregnancy. Uterine natural killer (uNK) cells are the predominant leukocyte population in the early pregnant decidua, and a role for these cells in spiral artery remodeling in pregnancy has been suggested. Angiogenic growth factors were measured in isolated uNK and total (unseparated) decidual cells (8-10 or 12-14 weeks gestation, n=5 each gestational age) after culture for 48 h. Angiopoietin (Ang)1, placental growth factor, transforming growth factor-beta1 (TGF-beta1), and vascular endothelial growth factor (VEGF)-C were measured by enzyme-linked immunosorbent assay. Angiogenin, Ang2, fibroblast growth factor basic, intercellular adhesion molecule (ICAM)-1, keratinocyte growth factor (KGF), platelet-derived growth factor-BB, and VEGF-A were measured using a FASTQuant angiogenic growth factor multiplex protein assay. Levels of Ang2, ICAM-1, and KGF, secreted by the total decidual fraction, decreased with increasing gestational age. uNK levels of Ang2 and VEGF-C also decreased with increasing gestational age. At 8-10 weeks gestation, there was no difference in the level of Ang1, Ang2, TGF-beta1, and VEGF-C secreted by uNK cells and the total decidual fraction. At 12-14 weeks, uNK cells secreted significantly lower levels of VEGF-C than the total decidual fraction. Early pregnancy decidua is a major source of angiogenic growth factors whose levels decrease with increasing gestational age, suggesting that they may play a role in spiral artery remodeling. uNK cells appear to be a prominent source of Ang1, Ang2, TGF-beta1, and VEGF-C within the placental bed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0741-5400
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
80
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
572-80
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pubmed:meshHeading |
pubmed-meshheading:16816146-Angiogenic Proteins,
pubmed-meshheading:16816146-Female,
pubmed-meshheading:16816146-Gene Expression Regulation,
pubmed-meshheading:16816146-Humans,
pubmed-meshheading:16816146-Killer Cells, Natural,
pubmed-meshheading:16816146-Pregnancy,
pubmed-meshheading:16816146-Pregnancy Trimester, First,
pubmed-meshheading:16816146-Pregnancy Trimester, Second,
pubmed-meshheading:16816146-RNA, Messenger,
pubmed-meshheading:16816146-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:16816146-Sensitivity and Specificity,
pubmed-meshheading:16816146-Transforming Growth Factor beta1,
pubmed-meshheading:16816146-Uterus
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pubmed:year |
2006
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pubmed:articleTitle |
Expression of angiogenic growth factors by uterine natural killer cells during early pregnancy.
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pubmed:affiliation |
School of Surgical and Reproductive Sciences, 3rd Floor, William Leech Building, University of Newcastle upon Tyne, Newcastle upon Tyne, NE2 4HH, UK. g.e.lash@ncl.ac.uk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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