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

Bibliographic Details
Main Author: Fonseca, Catarina Gonçalves
Publication Date: 2023
Other Authors: Silvério, Vânia, Barata, David, Giese, Wolfgang, Gerhardt, Holger, Cardoso, Susana, Franco, Cláudio Areias
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10400.14/42764
Summary: 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. [Figure not available: see fulltext.].
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spelling A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditionsThe 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. [Figure not available: see fulltext.].VeritatiFonseca, Catarina GonçalvesSilvério, VâniaBarata, DavidGiese, WolfgangGerhardt, HolgerCardoso, SusanaFranco, Cláudio Areias2023-10-04T13:12:41Z2023-122023-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.14/42764eng2055-743410.1038/s41378-023-00589-xinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-13T14:36:57Zoai:repositorio.ucp.pt:10400.14/42764Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T02:06:34.303609Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv 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
spellingShingle A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
Fonseca, Catarina Gonçalves
title_short 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_sort A 96-wells fluidic system for high-throughput screenings under laminar high wall shear stress conditions
author Fonseca, Catarina Gonçalves
author_facet Fonseca, Catarina Gonçalves
Silvério, Vânia
Barata, David
Giese, Wolfgang
Gerhardt, Holger
Cardoso, Susana
Franco, Cláudio Areias
author_role author
author2 Silvério, Vânia
Barata, David
Giese, Wolfgang
Gerhardt, Holger
Cardoso, Susana
Franco, Cláudio Areias
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Veritati
dc.contributor.author.fl_str_mv Fonseca, Catarina Gonçalves
Silvério, Vânia
Barata, David
Giese, Wolfgang
Gerhardt, Holger
Cardoso, Susana
Franco, Cláudio Areias
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. [Figure not available: see fulltext.].
publishDate 2023
dc.date.none.fl_str_mv 2023-10-04T13:12:41Z
2023-12
2023-12-01T00:00:00Z
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10.1038/s41378-023-00589-x
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