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A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions

The ability of endothelial cells to respond to blood flow is fundamental for the correct formation and maintenance of a functional and hierarchically organized vascular network. Defective flow responses, in particular related to high flow conditions, have been associated with atherosclerosis, stroke...

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Autores principales: Fonseca, Catarina Gonçalves, Silvério, Vânia, Barata, David, Giese, Wolfgang, Gerhardt, Holger, Cardoso, Susana, Franco, Claudio Areias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504069/
https://www.ncbi.nlm.nih.gov/pubmed/37719414
http://dx.doi.org/10.1038/s41378-023-00589-x
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author Fonseca, Catarina Gonçalves
Silvério, Vânia
Barata, David
Giese, Wolfgang
Gerhardt, Holger
Cardoso, Susana
Franco, Claudio Areias
author_facet Fonseca, Catarina Gonçalves
Silvério, Vânia
Barata, David
Giese, Wolfgang
Gerhardt, Holger
Cardoso, Susana
Franco, Claudio Areias
author_sort Fonseca, Catarina Gonçalves
collection PubMed
description The ability of endothelial cells to respond to blood flow is fundamental for the correct formation and maintenance of a functional and hierarchically organized vascular network. Defective flow responses, in particular related to high flow conditions, have been associated with atherosclerosis, stroke, arteriovenous malformations, and neurodegenerative diseases. Yet, the molecular mechanisms involved in high flow response are still poorly understood. Here, we described the development and validation of a 96-wells fluidic system, with interchangeable cell culture and fluidics, to perform high-throughput screenings under laminar high-flow conditions. We demonstrated that endothelial cells in our newly developed 96-wells fluidic system respond to fluid flow-induced shear stress by aligning along the flow direction and increasing the levels of KLF2 and KLF4. We further demonstrate that our 96-wells fluidic system allows for efficient gene knock-down compatible with automated liquid handling for high-throughput screening platforms. Overall, we propose that this modular 96-well fluidic system is an excellent platform to perform genome-wide and/or drug screenings to identify the molecular mechanisms involved in the responses of endothelial cells to high wall shear stress. [Image: see text]
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spelling pubmed-105040692023-09-17 A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions Fonseca, Catarina Gonçalves Silvério, Vânia Barata, David Giese, Wolfgang Gerhardt, Holger Cardoso, Susana Franco, Claudio Areias Microsyst Nanoeng Article The ability of endothelial cells to respond to blood flow is fundamental for the correct formation and maintenance of a functional and hierarchically organized vascular network. Defective flow responses, in particular related to high flow conditions, have been associated with atherosclerosis, stroke, arteriovenous malformations, and neurodegenerative diseases. Yet, the molecular mechanisms involved in high flow response are still poorly understood. Here, we described the development and validation of a 96-wells fluidic system, with interchangeable cell culture and fluidics, to perform high-throughput screenings under laminar high-flow conditions. We demonstrated that endothelial cells in our newly developed 96-wells fluidic system respond to fluid flow-induced shear stress by aligning along the flow direction and increasing the levels of KLF2 and KLF4. We further demonstrate that our 96-wells fluidic system allows for efficient gene knock-down compatible with automated liquid handling for high-throughput screening platforms. Overall, we propose that this modular 96-well fluidic system is an excellent platform to perform genome-wide and/or drug screenings to identify the molecular mechanisms involved in the responses of endothelial cells to high wall shear stress. [Image: see text] Nature Publishing Group UK 2023-09-15 /pmc/articles/PMC10504069/ /pubmed/37719414 http://dx.doi.org/10.1038/s41378-023-00589-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fonseca, Catarina Gonçalves
Silvério, Vânia
Barata, David
Giese, Wolfgang
Gerhardt, Holger
Cardoso, Susana
Franco, Claudio Areias
A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
title A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
title_full A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
title_fullStr A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
title_full_unstemmed A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
title_short A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
title_sort 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10504069/
https://www.ncbi.nlm.nih.gov/pubmed/37719414
http://dx.doi.org/10.1038/s41378-023-00589-x
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