Differential expression of Vegfr-2 and its soluble form in preeclampsia.
Several studies have suggested that the main features of preeclampsia (PE) are consequences of endothelial dysfunction related to excess circulating anti-angiogenic factors, most notably, soluble sVEGFR-1 (also known as sFlt-1) and soluble endoglin (sEng), as well as to decreased PlGF. Recently, sol...
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doaj-d07771b927044f0fb97b94e77484769b2020-11-25T00:24:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3347510.1371/journal.pone.0033475Differential expression of Vegfr-2 and its soluble form in preeclampsia.Carine MunautSophie LorquetChristel PequeuxCapucine CoulonJeanne Le GoarantFrédéric ChantraineAgnès NoëlFrédéric GoffinVassilis TsatsarisDamien SubtilJean-Michel FoidartSeveral studies have suggested that the main features of preeclampsia (PE) are consequences of endothelial dysfunction related to excess circulating anti-angiogenic factors, most notably, soluble sVEGFR-1 (also known as sFlt-1) and soluble endoglin (sEng), as well as to decreased PlGF. Recently, soluble VEGF type 2 receptor (sVEGFR-2) has emerged as a crucial regulator of lymphangiogenesis. To date, however, there is a paucity of information on the changes of VEGFR-2 that occur during the clinical onset of PE. Therefore, the aim of our study was to characterize the plasma levels of VEGFR-2 in PE patients and to perform VEGFR-2 immunolocalization in placenta.By ELISA, we observed that the VEGFR-2 plasma levels were reduced during PE compared with normal gestational age matched pregnancies, whereas the VEGFR-1 and Eng plasma levels were increased. The dramatic drop in the VEGFR-1 levels shortly after delivery confirmed its placental origin. In contrast, the plasma levels of Eng and VEGFR-2 decreased only moderately during the early postpartum period. An RT-PCR analysis showed that the relative levels of VEGFR-1, sVEGFR-1 and Eng mRNA were increased in the placentas of women with severe PE. The relative levels of VEGFR-2 mRNA as well as expressing cells, were similar in both groups. We also made the novel finding that a recently described alternatively spliced VEGFR-2 mRNA variant was present at lower relative levels in the preeclamptic placentas.Our results indicate that the plasma levels of anti-angiogenic factors, particularly VEGFR-1 and VEGFR-2, behave in different ways after delivery. The rapid decrease in plasma VEGFR-1 levels appears to be a consequence of the delivery of the placenta. The persistent circulating levels of VEGFR-2 suggest a maternal endothelial origin of this peptide. The decreased VEGFR-2 plasma levels in preeclamptic women may serve as a marker of endothelial dysfunction.http://europepmc.org/articles/PMC3299790?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Carine Munaut Sophie Lorquet Christel Pequeux Capucine Coulon Jeanne Le Goarant Frédéric Chantraine Agnès Noël Frédéric Goffin Vassilis Tsatsaris Damien Subtil Jean-Michel Foidart |
spellingShingle |
Carine Munaut Sophie Lorquet Christel Pequeux Capucine Coulon Jeanne Le Goarant Frédéric Chantraine Agnès Noël Frédéric Goffin Vassilis Tsatsaris Damien Subtil Jean-Michel Foidart Differential expression of Vegfr-2 and its soluble form in preeclampsia. PLoS ONE |
author_facet |
Carine Munaut Sophie Lorquet Christel Pequeux Capucine Coulon Jeanne Le Goarant Frédéric Chantraine Agnès Noël Frédéric Goffin Vassilis Tsatsaris Damien Subtil Jean-Michel Foidart |
author_sort |
Carine Munaut |
title |
Differential expression of Vegfr-2 and its soluble form in preeclampsia. |
title_short |
Differential expression of Vegfr-2 and its soluble form in preeclampsia. |
title_full |
Differential expression of Vegfr-2 and its soluble form in preeclampsia. |
title_fullStr |
Differential expression of Vegfr-2 and its soluble form in preeclampsia. |
title_full_unstemmed |
Differential expression of Vegfr-2 and its soluble form in preeclampsia. |
title_sort |
differential expression of vegfr-2 and its soluble form in preeclampsia. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2012-01-01 |
description |
Several studies have suggested that the main features of preeclampsia (PE) are consequences of endothelial dysfunction related to excess circulating anti-angiogenic factors, most notably, soluble sVEGFR-1 (also known as sFlt-1) and soluble endoglin (sEng), as well as to decreased PlGF. Recently, soluble VEGF type 2 receptor (sVEGFR-2) has emerged as a crucial regulator of lymphangiogenesis. To date, however, there is a paucity of information on the changes of VEGFR-2 that occur during the clinical onset of PE. Therefore, the aim of our study was to characterize the plasma levels of VEGFR-2 in PE patients and to perform VEGFR-2 immunolocalization in placenta.By ELISA, we observed that the VEGFR-2 plasma levels were reduced during PE compared with normal gestational age matched pregnancies, whereas the VEGFR-1 and Eng plasma levels were increased. The dramatic drop in the VEGFR-1 levels shortly after delivery confirmed its placental origin. In contrast, the plasma levels of Eng and VEGFR-2 decreased only moderately during the early postpartum period. An RT-PCR analysis showed that the relative levels of VEGFR-1, sVEGFR-1 and Eng mRNA were increased in the placentas of women with severe PE. The relative levels of VEGFR-2 mRNA as well as expressing cells, were similar in both groups. We also made the novel finding that a recently described alternatively spliced VEGFR-2 mRNA variant was present at lower relative levels in the preeclamptic placentas.Our results indicate that the plasma levels of anti-angiogenic factors, particularly VEGFR-1 and VEGFR-2, behave in different ways after delivery. The rapid decrease in plasma VEGFR-1 levels appears to be a consequence of the delivery of the placenta. The persistent circulating levels of VEGFR-2 suggest a maternal endothelial origin of this peptide. The decreased VEGFR-2 plasma levels in preeclamptic women may serve as a marker of endothelial dysfunction. |
url |
http://europepmc.org/articles/PMC3299790?pdf=render |
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