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Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis

BACKGROUND: The normal development of the uteroplacental circulation in pregnancy depends on angiogenic and vasodilatory factors such as vascular endothelial growth factor (VEGF). Reduced uterine artery blood flow (UABF) is a common cause of fetal growth restriction; abnormalities in angiogenic fact...

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Autores principales: Mehta, Vedanta, Abi-Nader, Khalil N., Shangaris, Panicos, Shaw, S. W. Steven, Filippi, Elisa, Benjamin, Elizabeth, Boyd, Michael, Peebles, Donald M., Martin, John, Zachary, Ian, David, Anna L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076190/
https://www.ncbi.nlm.nih.gov/pubmed/24977408
http://dx.doi.org/10.1371/journal.pone.0100021
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author Mehta, Vedanta
Abi-Nader, Khalil N.
Shangaris, Panicos
Shaw, S. W. Steven
Filippi, Elisa
Benjamin, Elizabeth
Boyd, Michael
Peebles, Donald M.
Martin, John
Zachary, Ian
David, Anna L.
author_facet Mehta, Vedanta
Abi-Nader, Khalil N.
Shangaris, Panicos
Shaw, S. W. Steven
Filippi, Elisa
Benjamin, Elizabeth
Boyd, Michael
Peebles, Donald M.
Martin, John
Zachary, Ian
David, Anna L.
author_sort Mehta, Vedanta
collection PubMed
description BACKGROUND: The normal development of the uteroplacental circulation in pregnancy depends on angiogenic and vasodilatory factors such as vascular endothelial growth factor (VEGF). Reduced uterine artery blood flow (UABF) is a common cause of fetal growth restriction; abnormalities in angiogenic factors are implicated. Previously we showed that adenovirus (Ad)-mediated VEGF-A(165) expression in the pregnant sheep uterine artery (UtA) increased nitric oxide synthase (NOS) expression, altered vascular reactivity and increased UABF. VEGF-D is a VEGF family member that promotes angiogenesis and vasodilatation but, in contrast to VEGF-A, does not increase vascular permeability. Here we examined the effect of Ad.VEGF-D(ΔNΔC) vector encoding a fully processed form of VEGF-D, on the uteroplacental circulation. METHODS: UtA transit-time flow probes and carotid artery catheters were implanted in mid-gestation pregnant sheep (n = 5) to measure baseline UABF and maternal haemodynamics respectively. 7–14 days later, after injection of Ad.VEGF-D(ΔNΔC) vector (5×10(11) particles) into one UtA and an Ad vector encoding β-galactosidase (Ad.LacZ) contralaterally, UABF was measured daily until scheduled post-mortem examination at term. UtAs were assessed for vascular reactivity, NOS expression and endothelial cell proliferation; NOS expression was studied in ex vivo transduced UtA endothelial cells (UAECs). RESULTS: At 4 weeks post-injection, Ad.VEGF-D(ΔNΔC) treated UtAs showed significantly lesser vasoconstriction (E(max)144.0 v/s 184.2, p = 0.002). There was a tendency to higher UABF in Ad.VEGF-D(ΔNΔC) compared to Ad.LacZ transduced UtAs (50.58% v/s 26.94%, p = 0.152). There was no significant effect on maternal haemodynamics. An increased number of proliferating endothelial cells and adventitial blood vessels were observed in immunohistochemistry. Ad.VEGF-D(ΔNΔC) expression in cultured UAECs upregulated eNOS and iNOS expression. CONCLUSIONS: Local over-expression of VEGF-D(ΔNΔC) in the UtAs of pregnant mid-gestation sheep reduced vasoconstriction, promoted endothelial cell proliferation and showed a trend towards increased UABF. Studies in cultured UAECs indicate that VEGF-D(ΔNΔC) may act in part through upregulation of eNOS and iNOS.
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spelling pubmed-40761902014-07-02 Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis Mehta, Vedanta Abi-Nader, Khalil N. Shangaris, Panicos Shaw, S. W. Steven Filippi, Elisa Benjamin, Elizabeth Boyd, Michael Peebles, Donald M. Martin, John Zachary, Ian David, Anna L. PLoS One Research Article BACKGROUND: The normal development of the uteroplacental circulation in pregnancy depends on angiogenic and vasodilatory factors such as vascular endothelial growth factor (VEGF). Reduced uterine artery blood flow (UABF) is a common cause of fetal growth restriction; abnormalities in angiogenic factors are implicated. Previously we showed that adenovirus (Ad)-mediated VEGF-A(165) expression in the pregnant sheep uterine artery (UtA) increased nitric oxide synthase (NOS) expression, altered vascular reactivity and increased UABF. VEGF-D is a VEGF family member that promotes angiogenesis and vasodilatation but, in contrast to VEGF-A, does not increase vascular permeability. Here we examined the effect of Ad.VEGF-D(ΔNΔC) vector encoding a fully processed form of VEGF-D, on the uteroplacental circulation. METHODS: UtA transit-time flow probes and carotid artery catheters were implanted in mid-gestation pregnant sheep (n = 5) to measure baseline UABF and maternal haemodynamics respectively. 7–14 days later, after injection of Ad.VEGF-D(ΔNΔC) vector (5×10(11) particles) into one UtA and an Ad vector encoding β-galactosidase (Ad.LacZ) contralaterally, UABF was measured daily until scheduled post-mortem examination at term. UtAs were assessed for vascular reactivity, NOS expression and endothelial cell proliferation; NOS expression was studied in ex vivo transduced UtA endothelial cells (UAECs). RESULTS: At 4 weeks post-injection, Ad.VEGF-D(ΔNΔC) treated UtAs showed significantly lesser vasoconstriction (E(max)144.0 v/s 184.2, p = 0.002). There was a tendency to higher UABF in Ad.VEGF-D(ΔNΔC) compared to Ad.LacZ transduced UtAs (50.58% v/s 26.94%, p = 0.152). There was no significant effect on maternal haemodynamics. An increased number of proliferating endothelial cells and adventitial blood vessels were observed in immunohistochemistry. Ad.VEGF-D(ΔNΔC) expression in cultured UAECs upregulated eNOS and iNOS expression. CONCLUSIONS: Local over-expression of VEGF-D(ΔNΔC) in the UtAs of pregnant mid-gestation sheep reduced vasoconstriction, promoted endothelial cell proliferation and showed a trend towards increased UABF. Studies in cultured UAECs indicate that VEGF-D(ΔNΔC) may act in part through upregulation of eNOS and iNOS. Public Library of Science 2014-06-30 /pmc/articles/PMC4076190/ /pubmed/24977408 http://dx.doi.org/10.1371/journal.pone.0100021 Text en © 2014 Mehta et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mehta, Vedanta
Abi-Nader, Khalil N.
Shangaris, Panicos
Shaw, S. W. Steven
Filippi, Elisa
Benjamin, Elizabeth
Boyd, Michael
Peebles, Donald M.
Martin, John
Zachary, Ian
David, Anna L.
Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis
title Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis
title_full Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis
title_fullStr Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis
title_full_unstemmed Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis
title_short Local Over-Expression of VEGF-D(ΔNΔC) in the Uterine Arteries of Pregnant Sheep Results in Long-Term Changes in Uterine Artery Contractility and Angiogenesis
title_sort local over-expression of vegf-d(δnδc) in the uterine arteries of pregnant sheep results in long-term changes in uterine artery contractility and angiogenesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076190/
https://www.ncbi.nlm.nih.gov/pubmed/24977408
http://dx.doi.org/10.1371/journal.pone.0100021
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