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Exploring Endothelial Expansion on a Chip
Angiogenesis is the development of new blood vessels from the existing vasculature. Its malfunction leads to the development of cancers and cardiovascular diseases qualified by the WHO as a leading cause of death worldwide. A better understanding of mechanisms regulating physiological and pathologic...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741423/ https://www.ncbi.nlm.nih.gov/pubmed/36502120 http://dx.doi.org/10.3390/s22239414 |
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author | Konopka, Joanna Kołodziejek, Dominik Flont, Magdalena Żuchowska, Agnieszka Jastrzębska, Elżbieta Brzózka, Zbigniew |
author_facet | Konopka, Joanna Kołodziejek, Dominik Flont, Magdalena Żuchowska, Agnieszka Jastrzębska, Elżbieta Brzózka, Zbigniew |
author_sort | Konopka, Joanna |
collection | PubMed |
description | Angiogenesis is the development of new blood vessels from the existing vasculature. Its malfunction leads to the development of cancers and cardiovascular diseases qualified by the WHO as a leading cause of death worldwide. A better understanding of mechanisms regulating physiological and pathological angiogenesis will potentially contribute to developing more effective treatments for those urgent issues. Therefore, the main goal of the following study was to design and manufacture an angiogenesis-on-a-chip microplatform, including cylindrical microvessels created by Viscous Finger Patterning (VFP) technique and seeded with HUVECs. While optimizing the VFP procedure, we have observed that lumen’s diameter decreases with a diminution of the droplet’s volume. The influence of Vascular Endothelial Growth Factor (VEGF) with a concentration of 5, 25, 50, and 100 ng/mL on the migration of HUVECs was assessed. VEGF’s solution with concentrations varying from 5 to 50 ng/mL reveals high angiogenic potential. The spatial arrangement of cells and their morphology were visualized by fluorescence and confocal microscopy. Migration of HUVECs toward loaded angiogenic stimuli has been initiated after overnight incubation. This research is the basis for developing more complex vascularized multi-organ-on-a-chip microsystems that could potentially be used for drug screening. |
format | Online Article Text |
id | pubmed-9741423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97414232022-12-11 Exploring Endothelial Expansion on a Chip Konopka, Joanna Kołodziejek, Dominik Flont, Magdalena Żuchowska, Agnieszka Jastrzębska, Elżbieta Brzózka, Zbigniew Sensors (Basel) Article Angiogenesis is the development of new blood vessels from the existing vasculature. Its malfunction leads to the development of cancers and cardiovascular diseases qualified by the WHO as a leading cause of death worldwide. A better understanding of mechanisms regulating physiological and pathological angiogenesis will potentially contribute to developing more effective treatments for those urgent issues. Therefore, the main goal of the following study was to design and manufacture an angiogenesis-on-a-chip microplatform, including cylindrical microvessels created by Viscous Finger Patterning (VFP) technique and seeded with HUVECs. While optimizing the VFP procedure, we have observed that lumen’s diameter decreases with a diminution of the droplet’s volume. The influence of Vascular Endothelial Growth Factor (VEGF) with a concentration of 5, 25, 50, and 100 ng/mL on the migration of HUVECs was assessed. VEGF’s solution with concentrations varying from 5 to 50 ng/mL reveals high angiogenic potential. The spatial arrangement of cells and their morphology were visualized by fluorescence and confocal microscopy. Migration of HUVECs toward loaded angiogenic stimuli has been initiated after overnight incubation. This research is the basis for developing more complex vascularized multi-organ-on-a-chip microsystems that could potentially be used for drug screening. MDPI 2022-12-02 /pmc/articles/PMC9741423/ /pubmed/36502120 http://dx.doi.org/10.3390/s22239414 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Konopka, Joanna Kołodziejek, Dominik Flont, Magdalena Żuchowska, Agnieszka Jastrzębska, Elżbieta Brzózka, Zbigniew Exploring Endothelial Expansion on a Chip |
title | Exploring Endothelial Expansion on a Chip |
title_full | Exploring Endothelial Expansion on a Chip |
title_fullStr | Exploring Endothelial Expansion on a Chip |
title_full_unstemmed | Exploring Endothelial Expansion on a Chip |
title_short | Exploring Endothelial Expansion on a Chip |
title_sort | exploring endothelial expansion on a chip |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9741423/ https://www.ncbi.nlm.nih.gov/pubmed/36502120 http://dx.doi.org/10.3390/s22239414 |
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