A novel microfluidic platform for high-resolution imaging of a three-dimensional cell culture under a controlled hypoxic environment.

Low oxygen tensions experienced in various pathological and physiological conditions are a major stimulus for angiogenesis. Hypoxic conditions play a critical role in regulating cellular behaviour including migration, proliferation and differentiation. This study introduces the use of a microfluidic device that allows for the control of oxygen tension for the study of different three-dimensional (3D) cell cultures for various applications. The device has a central 3D gel region acting as an external cellular matrix, flanked by media channels. On each side, there is a peripheral gas channel through which suitable gas mixtures are supplied to establish a uniform oxygen tension or gradient within the device. The effects of various parameters, such as gas and media flow rates, device thickness, and diffusion coefficients of oxygen were examined using numerical simulations to determine the characteristics of the microfluidic device. A polycarbonate (PC) film with a low oxygen diffusion coefficient was embedded in the device in proximity above the channels to prevent oxygen diffusion from the incubator environment into the polydimethylsiloxane (PDMS) device. The oxygen tension in the device was then validated experimentally using a ruthenium-coated (Ru-coated) oxygen-sensing glass cover slip which confirmed the establishment of low uniform oxygen tensions (<3%) or an oxygen gradient across the gel region. To demonstrate the utility of the microfluidic device for cellular experiments under hypoxic conditions, migratory studies of MDA-MB-231 human breast cancer cells were performed. The microfluidic device allowed for imaging cellular migration with high-resolution, exhibiting an enhanced migration in hypoxia in comparison to normoxia. This microfluidic device presents itself as a promising platform for the investigation of cellular behaviour in a 3D gel scaffold under varying hypoxic conditions.

[1]  Ulrike Haessler,et al.  Migration dynamics of breast cancer cells in a tunable 3D interstitial flow chamber. , 2012, Integrative biology : quantitative biosciences from nano to macro.

[2]  Patrick Ymele-Leki,et al.  Fluorescent microparticles for sensing cell microenvironment oxygen levels within 3D scaffolds. , 2009, Biomaterials.

[3]  S. A. Stern,et al.  Diffusion of Gases in Silicone Polymers: Molecular Dynamics Simulations , 1998 .

[4]  Chien-Chung Peng,et al.  Generation of oxygen gradients in microfluidic devices for cell culture using spatially confined chemical reactions. , 2011, Lab on a chip.

[5]  Alan Wells,et al.  2D protrusion but not motility predicts growth factor–induced cancer cell migration in 3D collagen , 2012, The Journal of cell biology.

[6]  Roger D Kamm,et al.  A microfluidic platform for studying the effects of small temperature gradients in an incubator environment. , 2008, Biomicrofluidics.

[7]  P. Walczak,et al.  Hypoxia increases breast cancer cell-induced lymphatic endothelial cell migration. , 2008, Neoplasia.

[8]  Andrew Burgess,et al.  Loss of human Greatwall results in G2 arrest and multiple mitotic defects due to deregulation of the cyclin B-Cdc2/PP2A balance , 2010, Proceedings of the National Academy of Sciences.

[9]  Lionel Flamant,et al.  Anti-apoptotic role of HIF-1 and AP-1 in paclitaxel exposed breast cancer cells under hypoxia , 2010, Molecular Cancer.

[10]  R. Misra,et al.  Biomaterials , 2008 .

[11]  Hanry Yu,et al.  A practical guide to microfluidic perfusion culture of adherent mammalian cells. , 2007, Lab on a chip.

[12]  Shuichi Takayama,et al.  Quantitative measurement and control of oxygen levels in microfluidic poly(dimethylsiloxane) bioreactors during cell culture , 2007, Biomedical microdevices.

[13]  David T. Eddington,et al.  Modulating Temporal and Spatial Oxygenation over Adherent Cellular Cultures , 2009, PloS one.

[14]  A. Elias,et al.  Finite element analysis of oxygen transport in microfluidic cell culture devices with varying channel architectures, perfusion rates, and materials , 2011 .

[15]  Roger D. Kamm,et al.  Microfluidic Platforms for Studies of Angiogenesis, Cell Migration, and Cell–Cell Interactions , 2010, Annals of Biomedical Engineering.

[16]  Leonard I Zon,et al.  Cell stem cell. , 2007, Cell stem cell.

[17]  Roger D Kamm,et al.  Microfluidic devices for studying heterotypic cell-cell interactions and tissue specimen cultures under controlled microenvironments. , 2011, Biomicrofluidics.

[18]  Y. Sakai,et al.  Low O2 metabolism of HepG2 cells cultured at high density in a 3D microstructured scaffold , 2009, Biomedical microdevices.

[19]  W. Koros,et al.  Gas transport in polymers based on bisphenol‐A , 1988 .

[20]  Dr. Andreas von Deimling Neoplasia , 1997, Laboratory investigation; a journal of technical methods and pathology.

[21]  R. Hill,et al.  Graded hypoxia modulates the invasive potential of HT1080 fibrosarcoma and MDA MB231 carcinoma cells , 2008, Clinical & Experimental Metastasis.

[22]  Todd Thorsen,et al.  Development of an integrated microfluidic platform for dynamic oxygen sensing and delivery in a flowing medium. , 2005, Lab on a chip.

[23]  R. Kamm,et al.  Three-dimensional microfluidic model for tumor cell intravasation and endothelial barrier function , 2012, Proceedings of the National Academy of Sciences.

[24]  Matthew H. M. Lim,et al.  Perfused multiwell plate for 3D liver tissue engineering. , 2010, Lab on a chip.

[25]  D. Eddington,et al.  Oxygen sensitive microwells. , 2010, Lab on a chip.

[26]  Richard P. Hill,et al.  The hypoxic tumour microenvironment and metastatic progression , 2004, Clinical & Experimental Metastasis.

[27]  O. Geschke,et al.  Microfluidic dissolved oxygen gradient generator biochip as a useful tool in bacterial biofilm studies. , 2010, Lab on a chip.

[28]  P. Vaupel,et al.  Tumor hypoxia: definitions and current clinical, biologic, and molecular aspects. , 2001, Journal of the National Cancer Institute.

[29]  Alfredo Quiñones-Hinojosa,et al.  Oxygen in stem cell biology: a critical component of the stem cell niche. , 2010, Cell stem cell.

[30]  David T Eddington,et al.  Oxygen gradients for open well cellular cultures via microfluidic substrates. , 2010, Lab on a chip.

[31]  C. Tanford Macromolecules , 1994, Nature.

[32]  C. White,et al.  Limitations to oxygen diffusion and equilibration in in vitro cell exposure systems in hyperoxia and hypoxia. , 2001, American journal of physiology. Lung cellular and molecular physiology.

[33]  T. Moriya,et al.  Effects of Oxygen Concentration on the Proliferation and Differentiation of Mouse Neural Stem Cells In Vitro , 2008, Cellular and Molecular Neurobiology.

[34]  Paolo A Netti,et al.  Oxygen consumption of chondrocytes in agarose and collagen gels: a comparative analysis. , 2008, Biomaterials.

[35]  Mark E. Polinkovsky,et al.  Fine temporal control of the medium gas content and acidity and on-chip generation of series of oxygen concentrations for cell cultures. , 2009, Lab on a chip.

[36]  R. Hill,et al.  Acute (cyclic) hypoxia enhances spontaneous metastasis of KHT murine tumors. , 2001, Cancer research.

[37]  Farshid Guilak,et al.  An In Vitro System to Evaluate the Effects of Ischemia on Survival of Cells Used for Cell Therapy , 2007, Annals of Biomedical Engineering.

[38]  M. Russo,et al.  Role of hypoxia and autophagy in MDA‐MB‐231 invasiveness , 2010, Journal of cellular physiology.

[39]  Raymond H. W. Lam,et al.  Culturing Aerobic and Anaerobic Bacteria and Mammalian Cells with a Microfluidic Differential Oxygenator , 2009, Analytical chemistry.

[40]  L. Griffith,et al.  Transport‐mediated angiogenesis in 3D epithelial coculture , 2009, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[41]  R. Blasberg,et al.  Real-Time Imaging of HIF-1α Stabilization and Degradation , 2009, PloS one.

[42]  Roger D Kamm,et al.  A high-throughput microfluidic assay to study neurite response to growth factor gradients. , 2011, Lab on a chip.

[43]  Gordana Vunjak-Novakovic,et al.  Perfusion improves tissue architecture of engineered cardiac muscle. , 2002, Tissue engineering.

[44]  Vernella Vickerman,et al.  Design, fabrication and implementation of a novel multi-parameter control microfluidic platform for three-dimensional cell culture and real-time imaging. , 2008, Lab on a chip.

[45]  H. Redmond,et al.  Hypoxia increases the metastatic ability of breast cancer cells via upregulation of CXCR4 , 2010, BMC Cancer.

[46]  Nadine Kabbani,et al.  Enhanced Proliferation, Survival, and Dopaminergic Differentiation of CNS Precursors in Lowered Oxygen , 2000, The Journal of Neuroscience.

[47]  Tharathorn Rimchala,et al.  Surface‐Treatment‐Induced Three‐Dimensional Capillary Morphogenesis in a Microfluidic Platform , 2009, Advanced materials.

[48]  R. Motzer,et al.  High-dose chemotherapy and stem cell transplantation for advanced testicular cancer , 2011, Expert review of anticancer therapy.

[49]  P Vaupel,et al.  Oxygenation of human tumors: evaluation of tissue oxygen distribution in breast cancers by computerized O2 tension measurements. , 1991, Cancer research.

[50]  William J. Polacheck,et al.  Interstitial flow influences direction of tumor cell migration through competing mechanisms , 2011, Proceedings of the National Academy of Sciences.

[51]  Mark E. Polinkovsky,et al.  Generation of oxygen gradients with arbitrary shapes in a microfluidic device. , 2010, Lab on a chip.

[52]  Ali Borhan,et al.  Three-Dimensional Simulations of Reactive Gas Uptake in Single Airway Bifurcations , 2007, Annals of Biomedical Engineering.

[53]  J. Bussink,et al.  Optical Sensor-Based Oxygen Tension Measurements Correspond with Hypoxia Marker Binding in Three Human Tumor Xenograft Lines , 2000, Radiation research.

[54]  Tim David,et al.  Patterning, integration and characterisation of polymer optical oxygen sensors for microfluidic devices. , 2008, Lab on a chip.

[55]  宁北芳,et al.  疟原虫var基因转换速率变化导致抗原变异[英]/Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A , 2005 .