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An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels
Therapeutic regulation of tissue vascularization has appeared as an attractive approach to treat a number of human diseases. In vivo neovascularization assays that reflect physiological and pathological formation of neovessels are important in this effort. In this report we present an assay where th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496524/ https://www.ncbi.nlm.nih.gov/pubmed/22918697 http://dx.doi.org/10.1007/s10456-012-9287-8 |
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author | Kilarski, Witold W. Petersson, Ludvig Fuchs, Peder Fredlund Zielinski, Marcin S. Gerwins, Pär |
author_facet | Kilarski, Witold W. Petersson, Ludvig Fuchs, Peder Fredlund Zielinski, Marcin S. Gerwins, Pär |
author_sort | Kilarski, Witold W. |
collection | PubMed |
description | Therapeutic regulation of tissue vascularization has appeared as an attractive approach to treat a number of human diseases. In vivo neovascularization assays that reflect physiological and pathological formation of neovessels are important in this effort. In this report we present an assay where the effects of activators and inhibitors of angiogenesis can be quantitatively and qualitatively measured. A provisional matrix composed of collagen I and fibrin was formed in a plastic cylinder and implanted onto the chick chorioallantoic membrane. A nylon mesh separated the implanted matrix from the underlying tissue to distinguish new from pre-existing vessels. Vascularization of the matrix in response to fibroblast growth factor-2 or platelet-derived growth factor-BB was scored in a double-blinded manner, or vessel density was measured using a semi-automated image analysis procedure. Thalidomide, fumagillin, U0126 and TGFβ inhibited neovessel growth while hydrocortisone exerted a negative and wortmannin a toxic effect on the pre-existing vasculature. This quantitative, inexpensive and rapid in vivo angiogenesis assay might be a valuable tool in screening and characterizing factors that influence wound or tumor induced vascularization and in assessing their effects on the normal vasculature. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10456-012-9287-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-3496524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-34965242012-11-15 An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels Kilarski, Witold W. Petersson, Ludvig Fuchs, Peder Fredlund Zielinski, Marcin S. Gerwins, Pär Angiogenesis Original Paper Therapeutic regulation of tissue vascularization has appeared as an attractive approach to treat a number of human diseases. In vivo neovascularization assays that reflect physiological and pathological formation of neovessels are important in this effort. In this report we present an assay where the effects of activators and inhibitors of angiogenesis can be quantitatively and qualitatively measured. A provisional matrix composed of collagen I and fibrin was formed in a plastic cylinder and implanted onto the chick chorioallantoic membrane. A nylon mesh separated the implanted matrix from the underlying tissue to distinguish new from pre-existing vessels. Vascularization of the matrix in response to fibroblast growth factor-2 or platelet-derived growth factor-BB was scored in a double-blinded manner, or vessel density was measured using a semi-automated image analysis procedure. Thalidomide, fumagillin, U0126 and TGFβ inhibited neovessel growth while hydrocortisone exerted a negative and wortmannin a toxic effect on the pre-existing vasculature. This quantitative, inexpensive and rapid in vivo angiogenesis assay might be a valuable tool in screening and characterizing factors that influence wound or tumor induced vascularization and in assessing their effects on the normal vasculature. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s10456-012-9287-8) contains supplementary material, which is available to authorized users. Springer Netherlands 2012-08-24 2012 /pmc/articles/PMC3496524/ /pubmed/22918697 http://dx.doi.org/10.1007/s10456-012-9287-8 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Kilarski, Witold W. Petersson, Ludvig Fuchs, Peder Fredlund Zielinski, Marcin S. Gerwins, Pär An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
title | An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
title_full | An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
title_fullStr | An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
title_full_unstemmed | An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
title_short | An in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
title_sort | in vivo neovascularization assay for screening regulators of angiogenesis and assessing their effects on pre-existing vessels |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3496524/ https://www.ncbi.nlm.nih.gov/pubmed/22918697 http://dx.doi.org/10.1007/s10456-012-9287-8 |
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