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Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation

Fetal growth restriction (FGR) affects 5–10% of pregnancies, leading to clinically significant fetal morbidity and mortality. FGR placentae frequently exhibit poor vascular branching, but the mechanisms driving this are poorly understood. We hypothesize that vascular structural malformation at the o...

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Autores principales: Tun, Win M., Yap, Choon Hwai, Saw, Shier Nee, James, Joanna L., Clark, Alys R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614400/
https://www.ncbi.nlm.nih.gov/pubmed/31285454
http://dx.doi.org/10.1038/s41598-019-46151-6
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author Tun, Win M.
Yap, Choon Hwai
Saw, Shier Nee
James, Joanna L.
Clark, Alys R.
author_facet Tun, Win M.
Yap, Choon Hwai
Saw, Shier Nee
James, Joanna L.
Clark, Alys R.
author_sort Tun, Win M.
collection PubMed
description Fetal growth restriction (FGR) affects 5–10% of pregnancies, leading to clinically significant fetal morbidity and mortality. FGR placentae frequently exhibit poor vascular branching, but the mechanisms driving this are poorly understood. We hypothesize that vascular structural malformation at the organ level alters microvascular shear stress, impairing angiogenesis. A computational model of placental vasculature predicted elevated placental micro-vascular shear stress in FGR placentae (0.2 Pa in severe FGR vs 0.05 Pa in normal placentae). Endothelial cells cultured under predicted FGR shear stresses migrated significantly slower and with greater persistence than in shear stresses predicted in normal placentae. These cell behaviors suggest a dominance of vessel elongation over branching. Taken together, these results suggest (1) poor vascular development increases vessel shear stress, (2) increased shear stress induces cell behaviors that impair capillary branching angiogenesis, and (3) impaired branching angiogenesis continues to drive elevated shear stress, jeopardizing further vascular formation. Inadequate vascular branching early in gestation could kick off this cyclic loop and continue to negatively impact placental angiogenesis throughout gestation.
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spelling pubmed-66144002019-07-17 Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation Tun, Win M. Yap, Choon Hwai Saw, Shier Nee James, Joanna L. Clark, Alys R. Sci Rep Article Fetal growth restriction (FGR) affects 5–10% of pregnancies, leading to clinically significant fetal morbidity and mortality. FGR placentae frequently exhibit poor vascular branching, but the mechanisms driving this are poorly understood. We hypothesize that vascular structural malformation at the organ level alters microvascular shear stress, impairing angiogenesis. A computational model of placental vasculature predicted elevated placental micro-vascular shear stress in FGR placentae (0.2 Pa in severe FGR vs 0.05 Pa in normal placentae). Endothelial cells cultured under predicted FGR shear stresses migrated significantly slower and with greater persistence than in shear stresses predicted in normal placentae. These cell behaviors suggest a dominance of vessel elongation over branching. Taken together, these results suggest (1) poor vascular development increases vessel shear stress, (2) increased shear stress induces cell behaviors that impair capillary branching angiogenesis, and (3) impaired branching angiogenesis continues to drive elevated shear stress, jeopardizing further vascular formation. Inadequate vascular branching early in gestation could kick off this cyclic loop and continue to negatively impact placental angiogenesis throughout gestation. Nature Publishing Group UK 2019-07-08 /pmc/articles/PMC6614400/ /pubmed/31285454 http://dx.doi.org/10.1038/s41598-019-46151-6 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tun, Win M.
Yap, Choon Hwai
Saw, Shier Nee
James, Joanna L.
Clark, Alys R.
Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
title Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
title_full Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
title_fullStr Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
title_full_unstemmed Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
title_short Differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
title_sort differences in placental capillary shear stress in fetal growth restriction may affect endothelial cell function and vascular network formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6614400/
https://www.ncbi.nlm.nih.gov/pubmed/31285454
http://dx.doi.org/10.1038/s41598-019-46151-6
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