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A Microfluidic System for the Investigation of Tumor Cell Extravasation

Metastatic dissemination of cancer cells is a very complex process. It includes the intravasation of cells into the metastatic pathways, their passive distribution within the blood or lymph flow, and their extravasation into the surrounding tissue. Crucial steps during extravasation are the adhesion...

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Autores principales: Kühlbach, Claudia, da Luz, Sabrina, Baganz, Frank, Hass, Volker C., Mueller, Margareta M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027408/
https://www.ncbi.nlm.nih.gov/pubmed/29882894
http://dx.doi.org/10.3390/bioengineering5020040
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author Kühlbach, Claudia
da Luz, Sabrina
Baganz, Frank
Hass, Volker C.
Mueller, Margareta M.
author_facet Kühlbach, Claudia
da Luz, Sabrina
Baganz, Frank
Hass, Volker C.
Mueller, Margareta M.
author_sort Kühlbach, Claudia
collection PubMed
description Metastatic dissemination of cancer cells is a very complex process. It includes the intravasation of cells into the metastatic pathways, their passive distribution within the blood or lymph flow, and their extravasation into the surrounding tissue. Crucial steps during extravasation are the adhesion of the tumor cells to the endothelium and their transendothelial migration. However, the molecular mechanisms that are underlying this process are still not fully understood. Novel three dimensional (3D) models for research on the metastatic cascade include the use of microfluidic devices. Different from two dimensional (2D) models, these devices take cell–cell, structural, and mechanical interactions into account. Here we introduce a new microfluidic device in order to study tumor extravasation. The device consists of three different parts, containing two microfluidic channels and a porous membrane sandwiched in between them. A smaller channel together with the membrane represents the vessel equivalent and is seeded separately with primary endothelial cells (EC) that are isolated from the lung artery. The second channel acts as reservoir to collect the migrated tumor cells. In contrast to many other systems, this device does not need an additional coating to allow EC growth, as the primary EC that is used produces their own basement membrane. VE-Cadherin, an endothelial adherence junction protein, was expressed in regular localization, which indicates a tight barrier function and cell–cell connections of the endothelium. The EC in the device showed in vivo-like behavior under flow conditions. The GFP-transfected tumor cells that were introduced were of epithelial or mesenchymal origin and could be observed by live cell imaging, which indicates tightly adherent tumor cells to the endothelial lining under different flow conditions. These results suggest that the new device can be used for research on molecular requirements, conditions, and mechanism of extravasation and its inhibition.
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spelling pubmed-60274082018-07-13 A Microfluidic System for the Investigation of Tumor Cell Extravasation Kühlbach, Claudia da Luz, Sabrina Baganz, Frank Hass, Volker C. Mueller, Margareta M. Bioengineering (Basel) Article Metastatic dissemination of cancer cells is a very complex process. It includes the intravasation of cells into the metastatic pathways, their passive distribution within the blood or lymph flow, and their extravasation into the surrounding tissue. Crucial steps during extravasation are the adhesion of the tumor cells to the endothelium and their transendothelial migration. However, the molecular mechanisms that are underlying this process are still not fully understood. Novel three dimensional (3D) models for research on the metastatic cascade include the use of microfluidic devices. Different from two dimensional (2D) models, these devices take cell–cell, structural, and mechanical interactions into account. Here we introduce a new microfluidic device in order to study tumor extravasation. The device consists of three different parts, containing two microfluidic channels and a porous membrane sandwiched in between them. A smaller channel together with the membrane represents the vessel equivalent and is seeded separately with primary endothelial cells (EC) that are isolated from the lung artery. The second channel acts as reservoir to collect the migrated tumor cells. In contrast to many other systems, this device does not need an additional coating to allow EC growth, as the primary EC that is used produces their own basement membrane. VE-Cadherin, an endothelial adherence junction protein, was expressed in regular localization, which indicates a tight barrier function and cell–cell connections of the endothelium. The EC in the device showed in vivo-like behavior under flow conditions. The GFP-transfected tumor cells that were introduced were of epithelial or mesenchymal origin and could be observed by live cell imaging, which indicates tightly adherent tumor cells to the endothelial lining under different flow conditions. These results suggest that the new device can be used for research on molecular requirements, conditions, and mechanism of extravasation and its inhibition. MDPI 2018-05-23 /pmc/articles/PMC6027408/ /pubmed/29882894 http://dx.doi.org/10.3390/bioengineering5020040 Text en © 2018 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kühlbach, Claudia
da Luz, Sabrina
Baganz, Frank
Hass, Volker C.
Mueller, Margareta M.
A Microfluidic System for the Investigation of Tumor Cell Extravasation
title A Microfluidic System for the Investigation of Tumor Cell Extravasation
title_full A Microfluidic System for the Investigation of Tumor Cell Extravasation
title_fullStr A Microfluidic System for the Investigation of Tumor Cell Extravasation
title_full_unstemmed A Microfluidic System for the Investigation of Tumor Cell Extravasation
title_short A Microfluidic System for the Investigation of Tumor Cell Extravasation
title_sort microfluidic system for the investigation of tumor cell extravasation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027408/
https://www.ncbi.nlm.nih.gov/pubmed/29882894
http://dx.doi.org/10.3390/bioengineering5020040
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