Spatial control of oxygen delivery to 3D cultures alters cancer cell growth and gene expression
William J. Wulftange, Michelle A. Rose, Marcial Garmendia-CedillosiD, Davi da Silva, Joanna E. Poprawski, Dhruv Srinivasachar, Taylor Sullivan, Langston Lim, Valery V. Bliskovsky, Matthew D. HalliD, Thomas J. PohidaiD, Robert W. RobeyiD, Nicole Y. Morgan, Michael M. GottesmaniD
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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