Cargando…
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...
Autores principales: | , , , , |
---|---|
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 |
_version_ | 1783336604656467968 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6027408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT kuhlbachclaudia amicrofluidicsystemfortheinvestigationoftumorcellextravasation AT daluzsabrina amicrofluidicsystemfortheinvestigationoftumorcellextravasation AT baganzfrank amicrofluidicsystemfortheinvestigationoftumorcellextravasation AT hassvolkerc amicrofluidicsystemfortheinvestigationoftumorcellextravasation AT muellermargaretam amicrofluidicsystemfortheinvestigationoftumorcellextravasation AT kuhlbachclaudia microfluidicsystemfortheinvestigationoftumorcellextravasation AT daluzsabrina microfluidicsystemfortheinvestigationoftumorcellextravasation AT baganzfrank microfluidicsystemfortheinvestigationoftumorcellextravasation AT hassvolkerc microfluidicsystemfortheinvestigationoftumorcellextravasation AT muellermargaretam microfluidicsystemfortheinvestigationoftumorcellextravasation |