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Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces
One of the major challenges in bone grafting is the lack of sufficient bone vascularization. A rapid and stable bone vascularization at an early stage of implantation is essential for optimal functioning of the bone graft. To address this, the ability of in situ TiO(2) nanofibrous surfaces fabricate...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756327/ https://www.ncbi.nlm.nih.gov/pubmed/26883761 http://dx.doi.org/10.1038/srep21828 |
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author | Tan, Ai Wen Liau, Ling Ling Chua, Kien Hui Ahmad, Roslina Akbar, Sheikh Ali Pingguan-Murphy, Belinda |
author_facet | Tan, Ai Wen Liau, Ling Ling Chua, Kien Hui Ahmad, Roslina Akbar, Sheikh Ali Pingguan-Murphy, Belinda |
author_sort | Tan, Ai Wen |
collection | PubMed |
description | One of the major challenges in bone grafting is the lack of sufficient bone vascularization. A rapid and stable bone vascularization at an early stage of implantation is essential for optimal functioning of the bone graft. To address this, the ability of in situ TiO(2) nanofibrous surfaces fabricated via thermal oxidation method to enhance the angiogenic potential of human umbilical vein endothelial cells (HUVECs) was investigated. The cellular responses of HUVECs on TiO(2) nanofibrous surfaces were studied through cell adhesion, cell proliferation, capillary-like tube formation, growth factors secretion (VEGF and BFGF), and angiogenic-endogenic-associated gene (VEGF, VEGFR2, BFGF, PGF, HGF, Ang-1, VWF, PECAM-1 and ENOS) expression analysis after 2 weeks of cell seeding. Our results show that TiO(2) nanofibrous surfaces significantly enhanced adhesion, proliferation, formation of capillary-like tube networks and growth factors secretion of HUVECs, as well as leading to higher expression level of all angiogenic-endogenic-associated genes, in comparison to unmodified control surfaces. These beneficial effects suggest the potential use of such surface nanostructures to be utilized as an advantageous interface for bone grafts as they can promote angiogenesis, which improves bone vascularization. |
format | Online Article Text |
id | pubmed-4756327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47563272016-02-25 Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces Tan, Ai Wen Liau, Ling Ling Chua, Kien Hui Ahmad, Roslina Akbar, Sheikh Ali Pingguan-Murphy, Belinda Sci Rep Article One of the major challenges in bone grafting is the lack of sufficient bone vascularization. A rapid and stable bone vascularization at an early stage of implantation is essential for optimal functioning of the bone graft. To address this, the ability of in situ TiO(2) nanofibrous surfaces fabricated via thermal oxidation method to enhance the angiogenic potential of human umbilical vein endothelial cells (HUVECs) was investigated. The cellular responses of HUVECs on TiO(2) nanofibrous surfaces were studied through cell adhesion, cell proliferation, capillary-like tube formation, growth factors secretion (VEGF and BFGF), and angiogenic-endogenic-associated gene (VEGF, VEGFR2, BFGF, PGF, HGF, Ang-1, VWF, PECAM-1 and ENOS) expression analysis after 2 weeks of cell seeding. Our results show that TiO(2) nanofibrous surfaces significantly enhanced adhesion, proliferation, formation of capillary-like tube networks and growth factors secretion of HUVECs, as well as leading to higher expression level of all angiogenic-endogenic-associated genes, in comparison to unmodified control surfaces. These beneficial effects suggest the potential use of such surface nanostructures to be utilized as an advantageous interface for bone grafts as they can promote angiogenesis, which improves bone vascularization. Nature Publishing Group 2016-02-17 /pmc/articles/PMC4756327/ /pubmed/26883761 http://dx.doi.org/10.1038/srep21828 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tan, Ai Wen Liau, Ling Ling Chua, Kien Hui Ahmad, Roslina Akbar, Sheikh Ali Pingguan-Murphy, Belinda Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces |
title | Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces |
title_full | Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces |
title_fullStr | Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces |
title_full_unstemmed | Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces |
title_short | Enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized TiO(2) nanofibrous surfaces |
title_sort | enhanced in vitro angiogenic behaviour of human umbilical vein endothelial cells on thermally oxidized tio(2) nanofibrous surfaces |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4756327/ https://www.ncbi.nlm.nih.gov/pubmed/26883761 http://dx.doi.org/10.1038/srep21828 |
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