Orderly arrangement of hepatocyte spheroids on a microfabricated chip.

This article describes a novel method for preparing several spherical multicellular aggregates (spheroids) that have almost the same diameter on a microfabricated chip. The chip, fabricated by a simple method that uses a micromilling system, consisted of several thousand cavities, 100-500 microm in diameter, in a triangular arrangement on a polystyrene plate. Although no spheroid was formed on any chip when cultured under stationary conditions, hepatocytes formed spheroids in the cavities when turning force was applied with a rotary shaker. Especially on the chip with cavities 300 microm in diameter, one spheroid formed in each cavity; an orderly array of spheroids (1100 spheroids/cm(2)) of almost the same diameter was constructed. Ammonia removal and albumin secretion by the spheroids on the chip continued to occur at initial levels for at least 14 days of culture. Enzyme P-450 activity of the spheroids was also maintained and detected on this transparent chip by fluorescence of resorufin converted from ethoxyresorufin. The spheroid microarray chip seems to be a promising cellular platform for various biomedical applications such as in cell-based biosensors for toxicological and pharmacological examinations, and in bioartificial livers.

[1]  Wei-Shou Hu,et al.  Mechanistics of formation and ultrastructural evaluation of hepatocyte spheroids , 1996, In Vitro Cellular & Developmental Biology - Animal.

[2]  K. Asano,et al.  Continued high albumin production by multicellular spheroids of adult rat hepatocytes formed in the presence of liver-derived proteoglycans. , 1989, Biochemical and biophysical research communications.

[3]  Smadar Cohen,et al.  Modeling mass transfer in hepatocyte spheroids via cell viability, spheroid size, and hepatocellular functions , 2004, Biotechnology and bioengineering.

[4]  Z. Gatmaitan,et al.  The biology of the bile canaliculus, 1993 , 1993, Hepatology.

[5]  Sangeeta N Bhatia,et al.  Engineering liver therapies for the future. , 2002, Tissue engineering.

[6]  F. Alvarez,et al.  Long-term culture of adult rat hepatocyte spheroids. , 1992, Experimental cell research.

[7]  L E Babiss,et al.  Transcriptional regulation of the albumin gene in cultured rat hepatocytes. Role of basement-membrane matrix. , 1990, Molecular biology & medicine.

[8]  L. Griffith,et al.  Tissue Engineering--Current Challenges and Expanding Opportunities , 2002, Science.

[9]  Lin KH,et al.  Long‐term maintenance of liver‐specific functions in three‐dimensional culture of adult rat hepatocytes with a porous gelatin sponge support , 1995, Biotechnology and applied biochemistry.

[10]  D. Wise,et al.  Expression of liver-specific functions by rat hepatocytes seeded in treated poly(lactic-co-glycolic) acid biodegradable foams. , 2001, Tissue engineering.

[11]  A. L. Wezel Growth of Cell-strains and Primary Cells on Micro-carriers in Homogeneous Culture , 1967, Nature.

[12]  K. Nakazawa,et al.  Novel hybrid Artificial Liver using Hepatocyte Organoids , 2002, The International journal of artificial organs.

[13]  M L Yarmush,et al.  Cell-cell interactions are essential for maintenance of hepatocyte function in collagen gel but not on matrigel. , 1997, Biotechnology and bioengineering.

[14]  K. Asano,et al.  Formation of multicellular spheroids composed of adult rat hepatocytes in dishes with positively charged surfaces and under other nonadherent environments. , 1990, Experimental cell research.

[15]  M. Suzuki,et al.  Large-Scale Preparation and Function of Porcine Hepatocyte Spheroids , 1996, The International journal of artificial organs.

[16]  N. Marceau,et al.  Spheroidal aggregate culture of rat liver cells: histotypic reorganization, biomatrix deposition, and maintenance of functional activities , 1985, The Journal of cell biology.

[17]  G. Whitesides,et al.  Patterned deposition of cells and proteins onto surfaces by using three-dimensional microfluidic systems. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[18]  M. Kamihira,et al.  Efficient induction of hepatocyte spheroids in a suspension culture using a water-soluble synthetic polymer as an artificial matrix. , 1998, Journal of biochemistry.

[19]  D L Taylor,et al.  Real-time molecular and cellular analysis: the new frontier of drug discovery. , 2001, Current opinion in biotechnology.

[20]  Masayuki Yamato,et al.  Novel approach for achieving double-layered cell sheets co-culture: overlaying endothelial cell sheets onto monolayer hepatocytes utilizing temperature-responsive culture dishes. , 2002, Journal of biomedical materials research.

[21]  T. Akaike,et al.  Regulation of differentiation and proliferation of rat hepatocytes by lactose-carrying polystyrene. , 2008, Artificial organs.

[22]  R Williams,et al.  Extracorporeal support and hepatocyte transplantation in acute liver failure and cirrhosis , 1999, Journal of gastroenterology and hepatology.

[23]  W. S. Hu,et al.  Receding cytochrome P450 activity in disassembling hepatocyte spheroids. , 1999, Tissue engineering.

[24]  K Sugimachi,et al.  Hybrid artificial liver using hepatocyte organoid culture. , 2001, Artificial organs.

[25]  J. Gerlach,et al.  Bioreactors for Hybrid Liver Support: Historical Aspects and Novel Designs , 1999, Annals of the New York Academy of Sciences.

[26]  J. Vacanti,et al.  Alternatives to liver transplantation: from hepatocyte transplantation to tissue-engineered organs. , 2000, Gastroenterology.

[27]  D E Ingber,et al.  Preparation of poly(glycolic acid) bonded fiber structures for cell attachment and transplantation. , 1993, Journal of biomedical materials research.

[28]  K Sugimachi,et al.  Efficacy of a Polyurethane Foam/Spheroid Artificial Liver by Using Human Hepatoblastoma Cell Line (Hep G2) , 2003, Cell transplantation.

[29]  Kohji Nakazawa,et al.  Hepatocyte Spheroids in Polyurethane Foams: Functional Analysis and Application for a Hybrid Artificial Liver , 1998 .

[30]  R Langer,et al.  Formation of Spheroidal Aggregates of Hepatocytes on Biodegradable Polymers Under Continuous-Flow Bioreactor Conditions* , 1998, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

[31]  Paul Schimmel,et al.  M411_3c 107..110 , 2001 .

[32]  K. Shakesheff,et al.  Long-term culture of functional liver tissue: three-dimensional coculture of primary hepatocytes and stellate cells. , 2003, Tissue engineering.