Spatial control of oxygen delivery to 3D cultures alters cancer cell growth and gene expression
W. J. Wulftange, M. A. Rose, M. Garmendia-Cedillos, D. da Silva, J. E. Poprawski, D. Srinivasachar, T. Sullivan, L. Lim, V. V. Bliskovsky, M. D. Hall, T. J. Pohida, R. W. Robey, N. Y. Morgan, M. M. Gottesman
Abstract
Commonly used monolayer cancer cell cultures fail to provide a physiologically relevant environment in terms of oxygen delivery. Here, we describe a three-dimensional bioreactor system where cancer cells are grown in Matrigel in modified 6-well plates. Oxygen is delivered to the cultures through a polydimethylsiloxane (PDMS) membrane at the bottom of the wells, with microfabricated PDMS pillars to control oxygen delivery. The plates receive 3% oxygen from below and 0% oxygen at the top surface of the media, providing a gradient of 3% to 0% oxygen. We compared growth and transcriptional profiles for cancer cells grown in Matrigel in the bioreactor, 3D cultures grown in 21% oxygen, and cells grown in a standard hypoxia chamber at 3% oxygen. Additionally, we compared gene expression of conventional 2D monolayer culture and 3D Matrigel culture in 21% oxygen. We conclude that controlled oxygen delivery may provide a more physiologically relevant 3D system.
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