Premium
Endothelial cell expression of adhesion molecules is induced by fetal plasma from pregnancies with umbilical placental vascular disease
Author(s) -
Wang Xin,
Athayde Neil,
Trudinger Brian
Publication year - 2002
Publication title -
bjog: an international journal of obstetrics and gynaecology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.157
H-Index - 164
eISSN - 1471-0528
pISSN - 1470-0328
DOI - 10.1111/j.1471-0528.2002.01240.x
Subject(s) - umbilical artery , fetus , umbilical vein , cell adhesion molecule , andrology , endothelium , medicine , endothelial stem cell , endocrinology , biology , immunology , pregnancy , in vitro , biochemistry , genetics
Objective To test the hypothesis that local production with spill into the fetal circulation of factor(s) injurious to endothelium is responsible for the vascular pathology present when the umbilical artery Doppler study is abnormal. Expression of adhesion molecules is a feature of endothelial cell activation. Design Case–control study. Setting University teaching hospital. Samples Fetal plasma was collected from 27 normal pregnancies, 39 pregnancies with umbilical placental vascular disease defined by abnormal umbilical artery Doppler and 11 pregnancies with pre‐eclampsia and normal umbilical artery Doppler. Methods Isolated and cultured human umbilical vein endothelial cells from normal pregnancies were incubated with fetal plasma from three study groups. mRNA expression of intercellular cell adhesion molecule‐1 (ICAM‐1), vascular cell adhesion molecule‐1 (VCAM‐1) and platelet‐endothelial cell adhesion molecule‐1 (PECAM‐1) were assessed by reverse transcription‐polymerase chain reaction. To confirm the occurrence of this in vivo , we measured the levels of soluble fractions of sICAM‐1, sVCAM‐1 and sPECAM‐1 in the fetal circulation in the fetal plasma used for endothelial cell incubation. Results The mRNA expression of ICAM‐1 [median 1.1 (interquartile range 0.5–1.9) vs 0.7 (0.3–1.2), P < 0.05 ] and PECAM‐1 [2.1 (1.2–3.0) vs 1.5 (0.7–2.1), P < 0.05 ] was significantly higher following incubation with fetal plasma from umbilical placental vascular disease compared with the normal group. There was no difference in the expression of VCAM‐1 [1.2 (0.9–1.8) vs 1.1 (0.8–1.6), ns]. The group with maternal pre‐eclampsia and normal umbilical artery Doppler did not differ from the normal group. In the umbilical placental vascular disease group, the results were similar in the presence or absence of pre‐eclampsia. For soluble fractions of the adhesion molecules released into the fetal circulation, we found the levels (ng/mL) of sICAM‐1 [median 248.5 (interquartile range 197.3–315.7) vs 174.2 (144.5–212.9), P < 0.05 ] and sPECAM‐1 [9.3 (6.2–11.1) vs 6.1 (5.4–7.7), P < 0.05 ] in fetal plasma to be significantly increased in the presence of umbilical placental vascular disease compared with the normal. Conclusions Vascular disease in the fetal umbilical placental circulation is associated with an elevation in mRNA expression by endothelial cells of ICAM‐1 and PECAM‐1. Our study provides evidence for endothelial cell activation and dysfunction in umbilical placental vascular disease. We speculate that the plasma factor(s) affecting the vessels of the umbilical villous tree is locally released by the trophoblast. The occurrence of the maternal syndrome of pre‐eclampsia appears to be independent of this.