Effects of interstitial flow on tumor cell migration

Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2010. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 80-84). === Interstitial flow is the convective transport of fluid through tissue extracellular matrix. This creeping flu...

Full description

Bibliographic Details
Main Author: Polacheck, William J. (William Joseph)
Other Authors: Roger Kamm.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2011
Subjects:
Online Access:http://hdl.handle.net/1721.1/61917
id ndltd-MIT-oai-dspace.mit.edu-1721.1-61917
record_format oai_dc
spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-619172019-05-02T16:27:09Z Effects of interstitial flow on tumor cell migration Polacheck, William J. (William Joseph) Roger Kamm. Massachusetts Institute of Technology. Dept. of Mechanical Engineering. Massachusetts Institute of Technology. Dept. of Mechanical Engineering. Mechanical Engineering. Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2010. Cataloged from PDF version of thesis. Includes bibliographical references (p. 80-84). Interstitial flow is the convective transport of fluid through tissue extracellular matrix. This creeping fluid flow has been shown to affect the morphology and migration of cells such as fibroblasts, cancer cells, endothelial cells, and mesenchymal stem cells. However, due to limitations in experimental procedures and apparatuses, the mechanism by which cells detect flow and the details and dynamics of the cellular response remain largely unknown. We developed a microfluidic cell culture system in which we can apply stable pressure gradients and fluid flow, and in which we can observe transient responses of breast cancer cells seeded in a 3D collagen type I scaffold. We employed this system to examine cell migration in the presence of interstitial flow to address the hypothesis that interstitial flow increases the metastatic potential of breast cancer cells. By varying the concentration of chemoattractants, we decoupled the mechanisms that provide the migratory stimulus and the directional stimulus to migrating breast cancer cells in the presence of a flow field. We found that cells migrated along streamlines in the presence of flow and that the strength of the flow field determined directional bias of migration along the streamline. We provide evidence that CCR7-dependent autologous chemotaxis is the mechanism by which cells migrate with the flow, while a competing CCR7-independent mechanism leads to migration against the flow. Furthermore, we demonstrate these competing mechanisms are a powerful migrational stimulus, which likely play an important role in development of metastatic disease. by William J. Polacheck. S.M. 2011-03-24T20:26:26Z 2011-03-24T20:26:26Z 2010 2010 Thesis http://hdl.handle.net/1721.1/61917 707100981 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 84 p. application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Mechanical Engineering.
spellingShingle Mechanical Engineering.
Polacheck, William J. (William Joseph)
Effects of interstitial flow on tumor cell migration
description Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2010. === Cataloged from PDF version of thesis. === Includes bibliographical references (p. 80-84). === Interstitial flow is the convective transport of fluid through tissue extracellular matrix. This creeping fluid flow has been shown to affect the morphology and migration of cells such as fibroblasts, cancer cells, endothelial cells, and mesenchymal stem cells. However, due to limitations in experimental procedures and apparatuses, the mechanism by which cells detect flow and the details and dynamics of the cellular response remain largely unknown. We developed a microfluidic cell culture system in which we can apply stable pressure gradients and fluid flow, and in which we can observe transient responses of breast cancer cells seeded in a 3D collagen type I scaffold. We employed this system to examine cell migration in the presence of interstitial flow to address the hypothesis that interstitial flow increases the metastatic potential of breast cancer cells. By varying the concentration of chemoattractants, we decoupled the mechanisms that provide the migratory stimulus and the directional stimulus to migrating breast cancer cells in the presence of a flow field. We found that cells migrated along streamlines in the presence of flow and that the strength of the flow field determined directional bias of migration along the streamline. We provide evidence that CCR7-dependent autologous chemotaxis is the mechanism by which cells migrate with the flow, while a competing CCR7-independent mechanism leads to migration against the flow. Furthermore, we demonstrate these competing mechanisms are a powerful migrational stimulus, which likely play an important role in development of metastatic disease. === by William J. Polacheck. === S.M.
author2 Roger Kamm.
author_facet Roger Kamm.
Polacheck, William J. (William Joseph)
author Polacheck, William J. (William Joseph)
author_sort Polacheck, William J. (William Joseph)
title Effects of interstitial flow on tumor cell migration
title_short Effects of interstitial flow on tumor cell migration
title_full Effects of interstitial flow on tumor cell migration
title_fullStr Effects of interstitial flow on tumor cell migration
title_full_unstemmed Effects of interstitial flow on tumor cell migration
title_sort effects of interstitial flow on tumor cell migration
publisher Massachusetts Institute of Technology
publishDate 2011
url http://hdl.handle.net/1721.1/61917
work_keys_str_mv AT polacheckwilliamjwilliamjoseph effectsofinterstitialflowontumorcellmigration
_version_ 1719040953345376256