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Microfluidic Technology in Vascular Research

Vascular cell biology is an area of research with great biomedical relevance. Vascular dysfunction is involved in major diseases such as atherosclerosis, diabetes, and cancer. However, when studying vascular cell biology in the laboratory, it is difficult to mimic the dynamic, three-dimensional micr...

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Detalles Bibliográficos
Autores principales: van der Meer, A. D., Poot, A. A., Duits, M. H. G., Feijen, J., Vermes, I.
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775250/
https://www.ncbi.nlm.nih.gov/pubmed/19911076
http://dx.doi.org/10.1155/2009/823148
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author van der Meer, A. D.
Poot, A. A.
Duits, M. H. G.
Feijen, J.
Vermes, I.
author_facet van der Meer, A. D.
Poot, A. A.
Duits, M. H. G.
Feijen, J.
Vermes, I.
author_sort van der Meer, A. D.
collection PubMed
description Vascular cell biology is an area of research with great biomedical relevance. Vascular dysfunction is involved in major diseases such as atherosclerosis, diabetes, and cancer. However, when studying vascular cell biology in the laboratory, it is difficult to mimic the dynamic, three-dimensional microenvironment that is found in vivo. Microfluidic technology offers unique possibilities to overcome this difficulty. In this review, an overview of the recent applications of microfluidic technology in the field of vascular biological research will be given. Examples of how microfluidics can be used to generate shear stresses, growth factor gradients, cocultures, and migration assays will be provided. The use of microfluidic devices in studying three-dimensional models of vascular tissue will be discussed. It is concluded that microfluidic technology offers great possibilities to systematically study vascular cell biology with setups that more closely mimic the in vivo situation than those that are generated with conventional methods.
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spelling pubmed-27752502009-11-12 Microfluidic Technology in Vascular Research van der Meer, A. D. Poot, A. A. Duits, M. H. G. Feijen, J. Vermes, I. J Biomed Biotechnol Review Article Vascular cell biology is an area of research with great biomedical relevance. Vascular dysfunction is involved in major diseases such as atherosclerosis, diabetes, and cancer. However, when studying vascular cell biology in the laboratory, it is difficult to mimic the dynamic, three-dimensional microenvironment that is found in vivo. Microfluidic technology offers unique possibilities to overcome this difficulty. In this review, an overview of the recent applications of microfluidic technology in the field of vascular biological research will be given. Examples of how microfluidics can be used to generate shear stresses, growth factor gradients, cocultures, and migration assays will be provided. The use of microfluidic devices in studying three-dimensional models of vascular tissue will be discussed. It is concluded that microfluidic technology offers great possibilities to systematically study vascular cell biology with setups that more closely mimic the in vivo situation than those that are generated with conventional methods. Hindawi Publishing Corporation 2009 2009-11-10 /pmc/articles/PMC2775250/ /pubmed/19911076 http://dx.doi.org/10.1155/2009/823148 Text en Copyright © 2009 A. D. van der Meer et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
van der Meer, A. D.
Poot, A. A.
Duits, M. H. G.
Feijen, J.
Vermes, I.
Microfluidic Technology in Vascular Research
title Microfluidic Technology in Vascular Research
title_full Microfluidic Technology in Vascular Research
title_fullStr Microfluidic Technology in Vascular Research
title_full_unstemmed Microfluidic Technology in Vascular Research
title_short Microfluidic Technology in Vascular Research
title_sort microfluidic technology in vascular research
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2775250/
https://www.ncbi.nlm.nih.gov/pubmed/19911076
http://dx.doi.org/10.1155/2009/823148
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