Review—Progress in concept and practice of growing anchorage-dependent mammalian cells in three dimension

SummaryTissue culture has played a major role in the rapid advances made in medical science in the past 50 yr. The full potential of the technique, however, is limited by the fact that growth of cells is usually restricted to a monolayer accompanied by major decreases in many of their tissue-specific functions. This has been shown to be due, in large part, to the inadequate oxygenation of cells growing in tissue culture dishes. Studies that show that the high charge density and rigidity of the plastic and glass surfaces used for culture are also major factors limiting growth of cells to a monolayer, are reviewed. A new culture system has been developed in which cells are grown on substrata made using perfluorocarbons (PFCs) coated with collagen type 1 and other adhesive factors. Perfluorocarbons have a much higher solubility for oxygen than water and have been used as oxygen delivery systems to protect cells from hypoxia. These new PFC-based substrata can provide both the optimal level of oxygen cells need to maintain differentiated functions and the flexible and weaker type of adhesion that allows cells to round up, interact with each other, and when provided with adequate nutritional support, to grow in three dimension.

[1]  E. Drioli,et al.  The Effect of Oxygen Transport Resistances on the Viability and Functions of Isolated Rat Hepatocytes , 1996, The International journal of artificial organs.

[2]  Michael Szycher,et al.  Biocompatible polymers, metals, and composites , 1983 .

[3]  T. Tokiwa,et al.  Multilayer hepatocyte aggregates on porous expanded polytetrafluoroethylene , 1997, In Vitro Cellular & Developmental Biology - Animal.

[4]  D E Ingber,et al.  Cytoskeletal filament assembly and the control of cell spreading and function by extracellular matrix. , 1995, Journal of cell science.

[5]  L G Griffith,et al.  Cell-substratum adhesion strength as a determinant of hepatocyte aggregate morphology. , 1997, Biotechnology and bioengineering.

[6]  M. J. B. DAVY,et al.  Water Transport , 1947, Nature.

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

[8]  R. Winslow,et al.  Depression of endothelial and smooth muscle cell oxygen consumption by endotoxin. , 1998, American journal of physiology. Heart and circulatory physiology.

[9]  Kenneth M. Yamada,et al.  Fibronectin, integrins, and growth control , 2001, Journal of cellular physiology.

[10]  A Haverich,et al.  Enhanced oxygen delivery reverses anaerobic metabolic states in prolonged sandwich rat hepatocyte culture. , 1999, Experimental cell research.

[11]  B. Chance,et al.  Energy-Linked Pyridine Nucleotide Reduction: Inhibitory Effects of Hyperbaric Oxygen In Vitro and In Vivo , 1965, Nature.

[12]  W. Jelkmann,et al.  Pericellular PO2 and O2 consumption in monolayer cell cultures. , 1995, Respiration physiology.

[13]  K. Lowe,et al.  Perfluorochemicals: their applications and benefits to cell culture. , 1998, Trends in biotechnology.

[14]  T. Nakamura,et al.  Reciprocal modulation of growth and liver functions of mature rat hepatocytes in primary culture by an extract of hepatic plasma membranes. , 1984, The Journal of biological chemistry.

[15]  J. Folkman,et al.  Role of cell shape in growth control , 1978, Nature.

[16]  J. White,et al.  Evaluation of a hepatocyte‐entrapment hollow fiber bioreactor: A potential bioartificial liver , 1993, Biotechnology and bioengineering.

[17]  Hans Kresse,et al.  Proteoglycans of the extracellular matrix and growth control , 2001, Journal of cellular physiology.

[18]  M. Kempe,et al.  New perfluorocarbon system for multilayer growth of anchorage-dependent mammalian cells. , 2002, BioTechniques.

[19]  D. Häussinger,et al.  Functional significance of cell volume regulatory mechanisms. , 1998, Physiological reviews.

[20]  R. Tompkins,et al.  Oxygen uptake rates in cultured rat hepatocytes. , 1992, Biotechnology and bioengineering.

[21]  Leslie E. Blumenson,et al.  Kinetics of gas diffusion in mammalian cell culture systems. II. Theory , 1968 .

[22]  George K Michalopoulos,et al.  Liver regeneration. , 2005, Advances in biochemical engineering/biotechnology.

[23]  P. Kruse,et al.  PRODUCTION AND CHARACTERIZATION OF MULTIPLE-LAYERED POPULATIONS OF ANIMAL CELLS , 1965, The Journal of cell biology.

[24]  C. S. Chen,et al.  Geometric control of cell life and death. , 1997, Science.

[25]  C. Selden,et al.  Three‐dimensional in Vitro Cell Culture Leads to a Marked Upregulation of Cell Function in Human Hepatocyte Cell Lines‐an Important Tool for the Development of a Bioartificial Liver Machine , 1999, Annals of the New York Academy of Sciences.

[26]  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.

[27]  T. Nakamura,et al.  Reciprocal modulation of growth and differentiated functions of mature rat hepatocytes in primary culture by cell--cell contact and cell membranes. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[28]  W. Mueller‐Klieser Three-dimensional cell cultures: from molecular mechanisms to clinical applications. , 1997, American journal of physiology. Cell physiology.

[29]  W. Rumsey,et al.  Cellular energetics and the oxygen dependence of respiration in cardiac myocytes isolated from adult rat. , 1990, The Journal of biological chemistry.

[30]  H. Kleinman,et al.  Regulation of gene expression in adult rat hepatocytes cultured on a basement membrane matrix , 1988, Journal of cellular physiology.

[31]  R. Sutherland,et al.  A move for the better. , 1994, Environmental health perspectives.

[32]  G. Michalopoulos,et al.  Liver Regeneration , 1997, Science.

[33]  I. Giaever,et al.  Substrate mechanics and cell spreading. , 1991, Experimental cell research.

[34]  G. Bellomo,et al.  Sodium-mediated cell swelling is associated with irreversible damage in isolated hepatocytes exposed to hypoxia or mitochondrial toxins. , 1995, Biochemical and biophysical research communications.

[35]  W. Jelkmann,et al.  Microelectrode measurements of pericellular PO2 in erythropoietin-producing human hepatoma cell cultures. , 1993, The American journal of physiology.

[36]  Karl Brand,et al.  Aerobic glycolysis by proliferating cells: a protective strategy against reactive oxygen species 1 , 1997, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[37]  S. Nandi,et al.  Altered biochemical properties of mitochondria in mouse mammary epithelial cells during primary culture , 1977, Journal of cellular physiology.

[38]  R. Durand,et al.  Respiration-induced oxygen gradients in cultured mammalian cells. , 1990, International journal of radiation biology.

[39]  V. Gill,et al.  Endogenously generated active oxygen species and cellular glutathione levels in relation to BHK-21 cell proliferation. , 1994, Free radical research.

[40]  C. Rappaport An hypothesis on the role of cellular colloid osmotic pressure in determining behavior of cells in vitro including anchorage dependency and maintenance of the differentiated state. , 1984, Journal of theoretical biology.

[41]  K. S. Narayan,et al.  Three-dimensional growth patterns of various human tumor cell lines in simulated microgravity of a NASA bioreactor , 1997, In Vitro Cellular & Developmental Biology - Animal.

[42]  R. Tompkins,et al.  Optimization of hepatocyte attachment to microcarriers: Importance of oxygen , 1993, Biotechnology and bioengineering.

[43]  L. C. Clark,et al.  The solubility of oxygen in highly fluorinated liquids , 1977 .

[44]  Y. Wang,et al.  Cell locomotion and focal adhesions are regulated by substrate flexibility. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[45]  C. Boone,et al.  CONTACT INHIBITION, MACROMOLECULAR SYNTHESIS, AND POLYRIBOSOMES IN CULTURED HUMAN DIPLOID FIBROBLASTS. , 1965, Proceedings of the National Academy of Sciences of the United States of America.