Cargando…

Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress

One-way valves in the lymphatic system form from lymphatic endothelial cells (LECs) during embryonic development and are required for efficient tissue drainage. Although fluid flow is thought to guide both valve formation and maintenance, how this occurs at a mechanistic level remains incompletely u...

Descripción completa

Detalles Bibliográficos
Autores principales: Michalaki, Eleftheria, Surya, Vinay N., Fuller, Gerald G., Dunn, Alexander R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005002/
https://www.ncbi.nlm.nih.gov/pubmed/32029852
http://dx.doi.org/10.1038/s42003-019-0732-8
_version_ 1783494838371483648
author Michalaki, Eleftheria
Surya, Vinay N.
Fuller, Gerald G.
Dunn, Alexander R.
author_facet Michalaki, Eleftheria
Surya, Vinay N.
Fuller, Gerald G.
Dunn, Alexander R.
author_sort Michalaki, Eleftheria
collection PubMed
description One-way valves in the lymphatic system form from lymphatic endothelial cells (LECs) during embryonic development and are required for efficient tissue drainage. Although fluid flow is thought to guide both valve formation and maintenance, how this occurs at a mechanistic level remains incompletely understood. We built microfluidic devices that reproduce critical aspects of the fluid flow patterns found at sites of valvulogenesis. Using these devices, we observed that LECs replicated aspects of the early steps in valvulogenesis: cells oriented perpendicular to flow in the region of maximum wall shear stress (WSS) and exhibited enhanced nuclear localization of FOXC2, a transcription factor required for valvulogenesis. Further experiments revealed that the cell surface protein E-selectin was required for both of these responses. Our observations suggest that spatial gradients in WSS help to demarcate the locations of valve formation, and implicate E-selectin as a component of a mechanosensory process for detecting WSS gradients.
format Online
Article
Text
id pubmed-7005002
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70050022020-02-11 Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress Michalaki, Eleftheria Surya, Vinay N. Fuller, Gerald G. Dunn, Alexander R. Commun Biol Article One-way valves in the lymphatic system form from lymphatic endothelial cells (LECs) during embryonic development and are required for efficient tissue drainage. Although fluid flow is thought to guide both valve formation and maintenance, how this occurs at a mechanistic level remains incompletely understood. We built microfluidic devices that reproduce critical aspects of the fluid flow patterns found at sites of valvulogenesis. Using these devices, we observed that LECs replicated aspects of the early steps in valvulogenesis: cells oriented perpendicular to flow in the region of maximum wall shear stress (WSS) and exhibited enhanced nuclear localization of FOXC2, a transcription factor required for valvulogenesis. Further experiments revealed that the cell surface protein E-selectin was required for both of these responses. Our observations suggest that spatial gradients in WSS help to demarcate the locations of valve formation, and implicate E-selectin as a component of a mechanosensory process for detecting WSS gradients. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7005002/ /pubmed/32029852 http://dx.doi.org/10.1038/s42003-019-0732-8 Text en © The Author(s) 2020 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
Michalaki, Eleftheria
Surya, Vinay N.
Fuller, Gerald G.
Dunn, Alexander R.
Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
title Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
title_full Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
title_fullStr Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
title_full_unstemmed Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
title_short Perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
title_sort perpendicular alignment of lymphatic endothelial cells in response to spatial gradients in wall shear stress
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005002/
https://www.ncbi.nlm.nih.gov/pubmed/32029852
http://dx.doi.org/10.1038/s42003-019-0732-8
work_keys_str_mv AT michalakieleftheria perpendicularalignmentoflymphaticendothelialcellsinresponsetospatialgradientsinwallshearstress
AT suryavinayn perpendicularalignmentoflymphaticendothelialcellsinresponsetospatialgradientsinwallshearstress
AT fullergeraldg perpendicularalignmentoflymphaticendothelialcellsinresponsetospatialgradientsinwallshearstress
AT dunnalexanderr perpendicularalignmentoflymphaticendothelialcellsinresponsetospatialgradientsinwallshearstress