
Proceedings Paper
A bioMEMS device for the study of mechanical properties of cellsFormat | Member Price | Non-Member Price |
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Paper Abstract
The tumor microenvironment is a complex system which is not fully understood. New technologies are needed to provide a better understanding of the role of the tumor microenvironment in promoting metastasis. The Nano Intravital Device, or NANIVID, has been developed as an optically transparent, implantable tool to study the tumor microenvironment. Two etched glass substrates are sealed using a thin polymer membrane to create a reservoir with a single outlet. This reservoir is loaded with a custom hydrogel blend that contains selected factors for delivery to the tumor microenvironment. When the device is implanted in the tumor, the hydrogel swells and releases these entrapped molecules, forming a sustained concentration gradient. The NANIVID has previously been successful in manipulating the tumor microenvironment both in vitro as well as in vivo. As metastatic cells intravasate, it has been shown that some are able to do so unscathed and reach their new location, while others are cleaved during the process1. There appears to be a correlation between cell migration and the mechanical properties of these cells. It is believed that these properties can be detected in real time by atomic force microscopy. In this study, metastatic MTLn3 rat mammary cells are seeded onto 1-dimensional microfibers and directed up a stable gradient of growth factor. The NANIVID device is placed behind our AFM tip, where it generates a stable chemotactic gradient of epidermal growth factor. Scanning confocal laser microscopy is also used to monitor movement of the cells over time. This experiment will shed light on the mechanical changes in metastatic cells as they undergo directed migration.
Paper Details
Date Published: 5 March 2015
PDF: 8 pages
Proc. SPIE 9320, Microfluidics, BioMEMS, and Medical Microsystems XIII, 932017 (5 March 2015); doi: 10.1117/12.2078521
Published in SPIE Proceedings Vol. 9320:
Microfluidics, BioMEMS, and Medical Microsystems XIII
Bonnie L. Gray; Holger Becker, Editor(s)
PDF: 8 pages
Proc. SPIE 9320, Microfluidics, BioMEMS, and Medical Microsystems XIII, 932017 (5 March 2015); doi: 10.1117/12.2078521
Show Author Affiliations
Joseph M. Sanders, SUNY Polytechnic Institute (United States)
Logan Butt, SUNY College of Nanoscale Science and Engineering (United States)
Ashley Clark, SUNY Polytechnic Institute (United States)
James Williams, SUNY Polytechnic Institute (United States)
Michael Padgen, SUNY Polytechnic Institute (United States)
Logan Butt, SUNY College of Nanoscale Science and Engineering (United States)
Ashley Clark, SUNY Polytechnic Institute (United States)
James Williams, SUNY Polytechnic Institute (United States)
Michael Padgen, SUNY Polytechnic Institute (United States)
Edison Leung, Albert Einstein College of Medicine (United States)
Patricia Keely, Univ. of Wisconsin-Madison (United States)
John S. Condeelis, Albert Einstein College of Medicine (United States)
Julio Aguirre-Ghiso, Icahn School of Medicine at Mount Sinai (United States)
James Castracane, SUNY Polytechnic Institute (United States)
Patricia Keely, Univ. of Wisconsin-Madison (United States)
John S. Condeelis, Albert Einstein College of Medicine (United States)
Julio Aguirre-Ghiso, Icahn School of Medicine at Mount Sinai (United States)
James Castracane, SUNY Polytechnic Institute (United States)
Published in SPIE Proceedings Vol. 9320:
Microfluidics, BioMEMS, and Medical Microsystems XIII
Bonnie L. Gray; Holger Becker, Editor(s)
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