Stable immobilization of rat hepatocytes as hemispheroids onto collagen‐conjugated poly‐dimethylsiloxane (PDMS) surfaces: Importance of direct oxygenation through PDMS for both formation and function

The highly oxygen‐permeable material, poly‐dimethylsiloxane (PDMS), has the potential to be applied to cell culture microdevices, but cell detachment from PDMS has been a major problem. In this study, we demonstrate that a combination of collagen covalently immobilized PDMS and an adequate oxygen supply enables the establishment of a stable, attached spheroid (hemispheroid) culture of rat hepatocytes. The bottom PDMS surfaces were first treated with oxygen plasma, then coupled with aminosilane followed by a photoreactive crosslinker, and they were finally reacted with a collagen solution. X‐ray photoelectron spectroscopy (XPS) and contact angle measurements showed that the covalent immobilization of collagen on the surface occurred only where the crosslinker had been introduced. On the collagen‐conjugated PDMS surface, rat hepatocytes organized themselves into hemispheroids and maintained the viability and a remarkably high albumin production at least for 2 weeks of culture. In contrast, hepatocytes on the other types of PDMS surfaces formed suspended spheroids that had low albumin production. In addition, we showed that blocking the oxygen supply through the bottom PDMS surface inhibited the formation of hemispheroids and the augmentation of hepatocellular function. These results show that appropriate surface modification of PDMS is a promising approach towards the development of liver tissue microdevices. Biotechnol. Bioeng. 2008;99: 1472–1481. © 2007 Wiley Periodicals, Inc.

[1]  P. Seglen Preparation of isolated rat liver cells. , 1976, Methods in cell biology.

[2]  J. Vienken,et al.  Gas supply across membranes in bioreactors for hepatocyte culture. , 1990, Artificial organs.

[3]  M L Yarmush,et al.  Hepatocytes in collagen sandwich: evidence for transcriptional and translational regulation , 1992, The Journal of cell biology.

[4]  J. Gaylor,et al.  Techniques for Measurement of Oxygen Consumption Rates of Hepatocytes during Attachment and Post-Attachment , 1996, The International journal of artificial organs.

[5]  Y. Sakai,et al.  Comparisons of Porcine Hepatocyte Spheroids and Single Hepatocytes in the Non-Woven Fabric Bioartificial Liver Module , 1996, The International journal of artificial organs.

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

[7]  D. B. Kristensen,et al.  Pleiotrophin as a Swiss 3T3 cell-derived potent mitogen for adult rat hepatocytes. , 1999, Experimental cell research.

[8]  Y. Sakai,et al.  A New Bioartificial Liver Using Porcine Hepatocyte Spheroids in High-Cell-Density Suspension Perfusion Culture: In Vitro Performance in Synthesized Culture Medium and in 100% Human Plasma , 1999, Cell transplantation.

[9]  J. Vacanti,et al.  Silicon micromachining to tissue engineer branched vascular channels for liver fabrication. , 2000, Tissue engineering.

[10]  T. Merkel,et al.  Gas sorption, diffusion, and permeation in poly(dimethylsiloxane) , 2000 .

[11]  M. Toner,et al.  Effects of oxygenation and flow on the viability and function of rat hepatocytes cocultured in a microchannel flat-plate bioreactor. , 2001, Biotechnology and bioengineering.

[12]  L. Hansen,et al.  The role of actin filaments and microtubules in hepatocyte spheroid self-assembly. , 2001, Cell motility and the cytoskeleton.

[13]  Donald E Ingber,et al.  Micropatterning tractional forces in living cells. , 2002, Cell motility and the cytoskeleton.

[14]  L. Griffith,et al.  Functional behavior of primary rat liver cells in a three-dimensional perfused microarray bioreactor. , 2002, Tissue engineering.

[15]  L. Griffith,et al.  A microfabricated array bioreactor for perfused 3D liver culture. , 2002, Biotechnology and bioengineering.

[16]  Y. Sakai,et al.  Development of a biohybrid simulator for absorption and biotransformation processes in humans based on in vitro models of small intestine and liver tissues , 2003, Journal of Artificial Organs.

[17]  Hanry Yu,et al.  Galactosylated PVDF membrane promotes hepatocyte attachment and functional maintenance. , 2003, Biomaterials.

[18]  Y. Sakai,et al.  Enhanced in Vitro Maturation of Subcultivated Fetal Human Hepatocytes in Three Dimensional Culture using Poly-L-Lactic Acid Scaffolds in the Presence of Oncostatin M , 2003, The International journal of artificial organs.

[19]  S. Ostrovidov,et al.  Membrane-Based PDMS Microbioreactor for Perfused 3D Primary Rat Hepatocyte Cultures , 2004, Biomedical microdevices.

[20]  Yasuyuki Sakai,et al.  Long-term culture of primary rat hepatocytes with high albumin secretion using membrane-supported collagen sandwich , 2004, Cytotechnology.

[21]  K. Hirata,et al.  Bile canalicular formation in hepatic organoid reconstructed by rat small hepatocytes and nonparenchymal cells , 2004, Journal of cellular physiology.

[22]  G. Whitesides,et al.  Compatibility of mammalian cells on surfaces of poly(dimethylsiloxane). , 2004, Langmuir : the ACS journal of surfaces and colloids.

[23]  T. Kanamori,et al.  Optimal design of bio-hybrid systems with a hollow fiber scaffold: model analysis of oxygen diffusion/consumption , 2004 .

[24]  Teruo Fujii,et al.  Microfluidic PDMS (Polydimethylsiloxane) Bioreactor for Large‐Scale Culture of Hepatocytes , 2004, Biotechnology progress.

[25]  Masaki Nishikawa,et al.  Feasibility of a simple double-layered coculture system incorporating metabolic processes of the intestine and liver tissue: application to the analysis of benzo[a]pyrene toxicity. , 2004, Toxicology in vitro : an international journal published in association with BIBRA.

[26]  Y. Sakai,et al.  Fabrication of microstructures in photosensitive biodegradable polymers for tissue engineering applications. , 2004, Biomaterials.

[27]  Aaron Sin,et al.  Development of a Microscale Cell Culture Analog To Probe Naphthalene Toxicity , 2008, Biotechnology progress.

[28]  Seeram Ramakrishna,et al.  Three-dimensional co-culture of rat hepatocyte spheroids and NIH/3T3 fibroblasts enhances hepatocyte functional maintenance. , 2005, Acta biomaterialia.

[29]  J. West-Mays,et al.  EGF-grafted PDMS surfaces in artificial cornea applications. , 2005, Biomaterials.

[30]  Seeram Ramakrishna,et al.  Stable immobilization of rat hepatocyte spheroids on galactosylated nanofiber scaffold. , 2005, Biomaterials.

[31]  M. Toner,et al.  Microfabricated grooved substrates as platforms for bioartificial liver reactors. , 2005, Biotechnology and bioengineering.

[32]  Junji Fukuda,et al.  Orderly arrangement of hepatocyte spheroids on a microfabricated chip. , 2005, Tissue engineering.

[33]  L. Samson,et al.  A microscale in vitro physiological model of the liver: predictive screens for drug metabolism and enzyme induction. , 2005, Current drug metabolism.

[34]  Toshihiro Akaike,et al.  Enhanced liver functions of hepatocytes cocultured with NIH 3T3 in the alginate/galactosylated chitosan scaffold. , 2006, Biomaterials.

[35]  Junji Fukuda,et al.  Hepatocyte spheroid culture on a polydimethylsiloxane chip having microcavities , 2006, Journal of biomaterials science. Polymer edition.

[36]  Hongkai Wu,et al.  Phospholipid biotinylation of polydimethylsiloxane (PDMS) for protein immobilization. , 2006, Lab on a chip.

[37]  A. Khademhosseini,et al.  Microscale technologies for tissue engineering and biology. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[38]  P. Ducheyne,et al.  Nucleation and growth of calcium phosphate on amine-, carboxyl- and hydroxyl-silane self-assembled monolayers. , 2006, Biomaterials.

[39]  J. Wang,et al.  RGD peptide-conjugated poly(dimethylsiloxane) promotes adhesion, proliferation, and collagen secretion of human fibroblasts. , 2006, Journal of biomedical materials research. Part A.

[40]  Enrico Drioli,et al.  Long-term maintenance of human hepatocytes in oxygen-permeable membrane bioreactor. , 2006, Biomaterials.

[41]  M. Yarmush,et al.  A novel formulation of oxygen‐carrying matrix enhances liver‐specific function of cultured hepatocytes , 2006, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[42]  Cheng-Hsien Liu,et al.  Rapid heterogeneous liver-cell on-chip patterning via the enhanced field-induced dielectrophoresis trap. , 2006, Lab on a chip.

[43]  Junji Fukuda,et al.  Novel hepatocyte culture system developed using microfabrication and collagen/polyethylene glycol microcontact printing. , 2006, Biomaterials.

[44]  K. Jensen,et al.  Cells on chips , 2006, Nature.

[45]  P. Price,et al.  The Size Exclusion Characteristics of Type I Collagen , 2007, Journal of Biological Chemistry.

[46]  M. Toner,et al.  Oxygen uptake rates and liver‐specific functions of hepatocyte and 3T3 fibroblast co‐cultures , 2007, Biotechnology and bioengineering.