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Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms

Liver transplantation is the most common treatment for patients with end-stage liver failure. However, liver transplantation is greatly limited by a shortage of donors. Liver tissue engineering may offer an alternative by providing an implantable engineered liver. Currently, diverse types of enginee...

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Detalles Bibliográficos
Autores principales: Yahya, Wan Nurlina Wan, Kadri, Nahrizul Adib, Ibrahim, Fatimah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168452/
https://www.ncbi.nlm.nih.gov/pubmed/24991941
http://dx.doi.org/10.3390/s140711714
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author Yahya, Wan Nurlina Wan
Kadri, Nahrizul Adib
Ibrahim, Fatimah
author_facet Yahya, Wan Nurlina Wan
Kadri, Nahrizul Adib
Ibrahim, Fatimah
author_sort Yahya, Wan Nurlina Wan
collection PubMed
description Liver transplantation is the most common treatment for patients with end-stage liver failure. However, liver transplantation is greatly limited by a shortage of donors. Liver tissue engineering may offer an alternative by providing an implantable engineered liver. Currently, diverse types of engineering approaches for in vitro liver cell culture are available, including scaffold-based methods, microfluidic platforms, and micropatterning techniques. Active cell patterning via dielectrophoretic (DEP) force showed some advantages over other methods, including high speed, ease of handling, high precision and being label-free. This article summarizes liver function and regenerative mechanisms for better understanding in developing engineered liver. We then review recent advances in liver tissue engineering techniques and focus on DEP-based cell patterning, including microelectrode design and patterning configuration.
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spelling pubmed-41684522014-09-19 Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms Yahya, Wan Nurlina Wan Kadri, Nahrizul Adib Ibrahim, Fatimah Sensors (Basel) Review Liver transplantation is the most common treatment for patients with end-stage liver failure. However, liver transplantation is greatly limited by a shortage of donors. Liver tissue engineering may offer an alternative by providing an implantable engineered liver. Currently, diverse types of engineering approaches for in vitro liver cell culture are available, including scaffold-based methods, microfluidic platforms, and micropatterning techniques. Active cell patterning via dielectrophoretic (DEP) force showed some advantages over other methods, including high speed, ease of handling, high precision and being label-free. This article summarizes liver function and regenerative mechanisms for better understanding in developing engineered liver. We then review recent advances in liver tissue engineering techniques and focus on DEP-based cell patterning, including microelectrode design and patterning configuration. MDPI 2014-07-02 /pmc/articles/PMC4168452/ /pubmed/24991941 http://dx.doi.org/10.3390/s140711714 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 Review
Yahya, Wan Nurlina Wan
Kadri, Nahrizul Adib
Ibrahim, Fatimah
Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms
title Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms
title_full Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms
title_fullStr Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms
title_full_unstemmed Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms
title_short Cell Patterning for Liver Tissue Engineering via Dielectrophoretic Mechanisms
title_sort cell patterning for liver tissue engineering via dielectrophoretic mechanisms
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168452/
https://www.ncbi.nlm.nih.gov/pubmed/24991941
http://dx.doi.org/10.3390/s140711714
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