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Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems

Fibroblasts, which play an important role in biological seal formation and maintenance, determine the long-term success of percutaneous implants. In this study, well-defined microporous structures with micropore diameters of 10–60 µm were fabricated by microelectromechanical systems and their influe...

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Detalles Bibliográficos
Autores principales: Wei, Hongbo, Zhao, Lingzhou, Chen, Bangdao, Bai, Shizhu, Zhao, Yimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139887/
https://www.ncbi.nlm.nih.gov/pubmed/25054322
http://dx.doi.org/10.3390/ijms150712998
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author Wei, Hongbo
Zhao, Lingzhou
Chen, Bangdao
Bai, Shizhu
Zhao, Yimin
author_facet Wei, Hongbo
Zhao, Lingzhou
Chen, Bangdao
Bai, Shizhu
Zhao, Yimin
author_sort Wei, Hongbo
collection PubMed
description Fibroblasts, which play an important role in biological seal formation and maintenance, determine the long-term success of percutaneous implants. In this study, well-defined microporous structures with micropore diameters of 10–60 µm were fabricated by microelectromechanical systems and their influence on the fibroblast functionalities was observed. The results show that the microporous structures with micropore diameters of 10–60 µm did not influence the initial adherent fibroblast number; however, those with diameters of 40 and 50 µm improved the spread, actin stress fiber organization, proliferation and fibronectin secretion of the fibroblasts. The microporous structures with micropore diameters of 40–50 µm may be promising for application in the percutaneous part of an implant.
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spelling pubmed-41398872014-08-21 Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems Wei, Hongbo Zhao, Lingzhou Chen, Bangdao Bai, Shizhu Zhao, Yimin Int J Mol Sci Article Fibroblasts, which play an important role in biological seal formation and maintenance, determine the long-term success of percutaneous implants. In this study, well-defined microporous structures with micropore diameters of 10–60 µm were fabricated by microelectromechanical systems and their influence on the fibroblast functionalities was observed. The results show that the microporous structures with micropore diameters of 10–60 µm did not influence the initial adherent fibroblast number; however, those with diameters of 40 and 50 µm improved the spread, actin stress fiber organization, proliferation and fibronectin secretion of the fibroblasts. The microporous structures with micropore diameters of 40–50 µm may be promising for application in the percutaneous part of an implant. MDPI 2014-07-22 /pmc/articles/PMC4139887/ /pubmed/25054322 http://dx.doi.org/10.3390/ijms150712998 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Wei, Hongbo
Zhao, Lingzhou
Chen, Bangdao
Bai, Shizhu
Zhao, Yimin
Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems
title Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems
title_full Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems
title_fullStr Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems
title_full_unstemmed Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems
title_short Improved Fibroblast Functionalities by Microporous Pattern Fabricated by Microelectromechanical Systems
title_sort improved fibroblast functionalities by microporous pattern fabricated by microelectromechanical systems
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139887/
https://www.ncbi.nlm.nih.gov/pubmed/25054322
http://dx.doi.org/10.3390/ijms150712998
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