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Brain microvascular endothelial cells resist elongation due to curvature and shear stress

The highly specialized endothelial cells in brain capillaries are a key component of the blood-brain barrier, forming a network of tight junctions that almost completely block paracellular transport. In contrast to vascular endothelial cells in other organs, we show that brain microvascular endothel...

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Detalles Bibliográficos
Autores principales: Ye, Mao, Sanchez, Henry M., Hultz, Margot, Yang, Zhen, Bogorad, Max, Wong, Andrew D., Searson, Peter C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986701/
https://www.ncbi.nlm.nih.gov/pubmed/24732421
http://dx.doi.org/10.1038/srep04681
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author Ye, Mao
Sanchez, Henry M.
Hultz, Margot
Yang, Zhen
Bogorad, Max
Wong, Andrew D.
Searson, Peter C.
author_facet Ye, Mao
Sanchez, Henry M.
Hultz, Margot
Yang, Zhen
Bogorad, Max
Wong, Andrew D.
Searson, Peter C.
author_sort Ye, Mao
collection PubMed
description The highly specialized endothelial cells in brain capillaries are a key component of the blood-brain barrier, forming a network of tight junctions that almost completely block paracellular transport. In contrast to vascular endothelial cells in other organs, we show that brain microvascular endothelial cells resist elongation in response to curvature and shear stress. Since the tight junction network is defined by endothelial cell morphology, these results suggest that there may be an evolutionary advantage to resisting elongation by minimizing the total length of cell-cell junctions per unit length of vessel.
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spelling pubmed-39867012014-04-18 Brain microvascular endothelial cells resist elongation due to curvature and shear stress Ye, Mao Sanchez, Henry M. Hultz, Margot Yang, Zhen Bogorad, Max Wong, Andrew D. Searson, Peter C. Sci Rep Article The highly specialized endothelial cells in brain capillaries are a key component of the blood-brain barrier, forming a network of tight junctions that almost completely block paracellular transport. In contrast to vascular endothelial cells in other organs, we show that brain microvascular endothelial cells resist elongation in response to curvature and shear stress. Since the tight junction network is defined by endothelial cell morphology, these results suggest that there may be an evolutionary advantage to resisting elongation by minimizing the total length of cell-cell junctions per unit length of vessel. Nature Publishing Group 2014-04-15 /pmc/articles/PMC3986701/ /pubmed/24732421 http://dx.doi.org/10.1038/srep04681 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images in this article are included in the article's Creative Commons license, unless indicated otherwise in the image credit; if the image is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the image. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Article
Ye, Mao
Sanchez, Henry M.
Hultz, Margot
Yang, Zhen
Bogorad, Max
Wong, Andrew D.
Searson, Peter C.
Brain microvascular endothelial cells resist elongation due to curvature and shear stress
title Brain microvascular endothelial cells resist elongation due to curvature and shear stress
title_full Brain microvascular endothelial cells resist elongation due to curvature and shear stress
title_fullStr Brain microvascular endothelial cells resist elongation due to curvature and shear stress
title_full_unstemmed Brain microvascular endothelial cells resist elongation due to curvature and shear stress
title_short Brain microvascular endothelial cells resist elongation due to curvature and shear stress
title_sort brain microvascular endothelial cells resist elongation due to curvature and shear stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986701/
https://www.ncbi.nlm.nih.gov/pubmed/24732421
http://dx.doi.org/10.1038/srep04681
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