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Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis

The tube formation assay is a widely used in vitro experiment model to evaluate angiogenic properties by measuring the formation of tubular structures from vascular endothelial cells (ECs). in vitro experimental results are crucial when considered the advisability of moving forward to in vivo studie...

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Autores principales: Lee, Hyunsook, Kang, Kyu-Tae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205943/
https://www.ncbi.nlm.nih.gov/pubmed/30402031
http://dx.doi.org/10.4196/kjpp.2018.22.6.705
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author Lee, Hyunsook
Kang, Kyu-Tae
author_facet Lee, Hyunsook
Kang, Kyu-Tae
author_sort Lee, Hyunsook
collection PubMed
description The tube formation assay is a widely used in vitro experiment model to evaluate angiogenic properties by measuring the formation of tubular structures from vascular endothelial cells (ECs). in vitro experimental results are crucial when considered the advisability of moving forward to in vivo studies. Thus, the additional attentions to the in vitro assay is necessary to improve the quality of the pre-clinical data, leading to better decision-making for successful drug discovery. In this study, we improved the tube formation assay system in three aspects. First, we used human endothelial colony forming cells (ECFCs), which are endothelial precursors that have a robust proliferative capacity and more defined angiogenic characteristics compared to mature ECs. Second, we utilized a real-time cell recorder to track the progression of tube formation for 48 hours. Third, to minimize analysis error due to the limited observation area, we used image-stitching software to increase the microscope field of view to a 2×2 stitched area from the 4× object lens. Our advanced tube formation assay system successfully demonstrated the time-dependent dynamic progression of tube formation in the presence and absence of VEGF and FGF-2. Vatalanib, VEGF inhibitor, was tested by our assay system. Of note, IC(50) values of vatalanib was different at each observation time point. Collectively, these results indicate that our advanced tube formation assay system replicates the dynamic progression of tube formation in response to angiogenic modulators. Therefore, this new system provides a sensitive and versatile assay model for evaluating pro- or anti-angiogenic drugs.
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spelling pubmed-62059432018-11-07 Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis Lee, Hyunsook Kang, Kyu-Tae Korean J Physiol Pharmacol Original Article The tube formation assay is a widely used in vitro experiment model to evaluate angiogenic properties by measuring the formation of tubular structures from vascular endothelial cells (ECs). in vitro experimental results are crucial when considered the advisability of moving forward to in vivo studies. Thus, the additional attentions to the in vitro assay is necessary to improve the quality of the pre-clinical data, leading to better decision-making for successful drug discovery. In this study, we improved the tube formation assay system in three aspects. First, we used human endothelial colony forming cells (ECFCs), which are endothelial precursors that have a robust proliferative capacity and more defined angiogenic characteristics compared to mature ECs. Second, we utilized a real-time cell recorder to track the progression of tube formation for 48 hours. Third, to minimize analysis error due to the limited observation area, we used image-stitching software to increase the microscope field of view to a 2×2 stitched area from the 4× object lens. Our advanced tube formation assay system successfully demonstrated the time-dependent dynamic progression of tube formation in the presence and absence of VEGF and FGF-2. Vatalanib, VEGF inhibitor, was tested by our assay system. Of note, IC(50) values of vatalanib was different at each observation time point. Collectively, these results indicate that our advanced tube formation assay system replicates the dynamic progression of tube formation in response to angiogenic modulators. Therefore, this new system provides a sensitive and versatile assay model for evaluating pro- or anti-angiogenic drugs. The Korean Physiological Society and The Korean Society of Pharmacology 2018-11 2018-10-25 /pmc/articles/PMC6205943/ /pubmed/30402031 http://dx.doi.org/10.4196/kjpp.2018.22.6.705 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Hyunsook
Kang, Kyu-Tae
Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
title Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
title_full Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
title_fullStr Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
title_full_unstemmed Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
title_short Advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
title_sort advanced tube formation assay using human endothelial colony forming cells for in vitro evaluation of angiogenesis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205943/
https://www.ncbi.nlm.nih.gov/pubmed/30402031
http://dx.doi.org/10.4196/kjpp.2018.22.6.705
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