Increased rate of chondrocyte aggregation in a wavy-walled bioreactor.

A novel wavy-walled bioreactor designed to enhance mixing at controlled shear stress levels was used to culture chondrocytes in suspension. Chondrocyte aggregation in suspensions mixed at 30, 50, and 80 rpm was characterized in the wavy-walled bioreactor and compared with that in conventional smooth-walled and baffled-walled spinner flask bioreactors. Aggregation was characterized in terms of the percentage of cells that aggregated over time, and aggregate size changes over time. The kinetics of chondrocyte aggregation observed in the bioreactors was composed of two phases: early aggregation between 0 and 2 h of culture, and late aggregation between 3 and 24 h of culture. At 50 rpm, the kinetics of early aggregation in the wavy-walled bioreactor was approximately 25% and 65% faster, respectively, than those in the smooth-walled and baffled-walled spinner flask bioreactors. During the late aggregation phase, the kinetics of aggregation in the wavy-walled bioreactor were approximately 45% and 65% faster, respectively, than in the smooth-walled and baffled-walled spinner flasks. The observed improved kinetics of chondrocyte aggregation was obtained at no cost to the cell survival rate. Results of computerized image analysis suggest that chondrocyte aggregation occurred initially by the formation of new aggregates via cell-cell interactions and later by the joining of small aggregates into larger cell clumps. Aggregates appeared to grow for only a couple of hours in culture before reaching a steady size, possibly determined by limitations imposed by the hydrodynamic environment. These results suggest that the novel geometry of the wavy-walled bioreactor generates a hydrodynamic environment distinct from those traditionally used to culture engineered cartilage. Such differences may be useful in studies aimed at distinguishing the effects of the hydrodynamic environment on tissue-engineered cartilage. Characterizing the wavy-walled bioreactor's hydrodynamic environment and its effects on cartilage cell/tissue culture can help establish direct relationships between hydrodynamic forces and engineered tissue properties.

[1]  J. Abbott,et al.  THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS , 1966, The Journal of cell biology.

[2]  L. Freed Tissue culture bioreactors ; chondrogenesis as a model system , 1997 .

[3]  Gordana Vunjak-Novakovic,et al.  Effects of mixing on the composition and morphology of tissue‐engineered cartilage , 1996 .

[4]  R Langer,et al.  Neocartilage formation in vitro and in vivo using cells cultured on synthetic biodegradable polymers. , 1993, Journal of biomedical materials research.

[5]  G. Vunjak‐Novakovic,et al.  Cultivation of cell–polymer tissue constructs in simulated microgravity , 1995, Biotechnology and bioengineering.

[6]  G. Vunjak‐Novakovic,et al.  Composition of cell‐polymer cartilage implants , 1994, Biotechnology and bioengineering.

[7]  Jennie P. Mather,et al.  Mammalian Cell Culture , 1984, Springer US.

[8]  T. Wick,et al.  Concentric Cylinder Bioreactor for Production of Tissue Engineered Cartilage: Effect of Seeding Density and Hydrodynamic Loading on Construct Development , 2003, Biotechnology progress.

[9]  Robert L Sah,et al.  Perfusion increases cell content and matrix synthesis in chondrocyte three-dimensional cultures. , 2002, Tissue engineering.

[10]  J. Veldhuijzen,et al.  Aggregated chondrocytes as a model system to study cartilage metabolism. , 1982, Experimental cell research.

[11]  R Langer,et al.  Kinetics of chondrocyte growth in cell‐polymer implants , 1994, Biotechnology and bioengineering.

[12]  Suh-Chin Wu,et al.  Influence of hydrodynamic shear stress on microcarrier-attached cell growth: Cell line dependency and surfactant protection , 1999 .

[13]  E. Kastenbauer,et al.  Cartilage tissue engineering with novel nonwoven structured biomaterial based on hyaluronic acid benzyl ester. , 1998, Journal of biomedical materials research.

[14]  R Langer,et al.  Dynamic Cell Seeding of Polymer Scaffolds for Cartilage Tissue Engineering , 1998, Biotechnology progress.

[15]  K. Nilsson,et al.  Mammalian cell culture. , 1987, Methods in enzymology.

[16]  B. Obradovic,et al.  Bioreactor cultivation conditions modulate the composition and mechanical properties of tissue‐engineered cartilage , 1999, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[17]  Vassilios Sikavitsas,et al.  Tissue Engineering Bioreactors , 2006 .

[18]  M S Croughan,et al.  Growth and death in overagitated microcarrier cell cultures , 1989, Biotechnology and bioengineering.

[19]  R Langer,et al.  Chondrogenesis in a cell-polymer-bioreactor system. , 1998, Experimental cell research.

[20]  B. Lavietes Cellular interaction and chondrogenesis in vitro. , 1970, Developmental biology.

[21]  C. Heath,et al.  Influence of intermittent pressure, fluid flow, and mixing on the regenerative properties of articular chondrocytes. , 1999, Biotechnology and bioengineering.

[22]  A MOSCONA,et al.  Rotation-mediated histogenetic aggregation of dissociated cells. A quantifiable approach to cell interactions in vitro. , 1961, Experimental cell research.

[23]  Ivan Martin,et al.  Recent Advances in Cartilage Tissue Engineering: From the Choice of Cell Sources to the Use of Bioreactors , 2002 .

[24]  Gordana Vunjak-Novakovic,et al.  CHAPTER 13 – TISSUE ENGINEERING BIOREACTORS , 2000 .

[25]  S. Badylak,et al.  Formation of a SIS–Cartilage Composite Graft in Vitro and Its Use in the Repair of Articular Cartilage Defects , 1998 .

[26]  K. Athanasiou,et al.  Ex vivo synthesis of articular cartilage. , 2000, Biomaterials.

[27]  R Cancedda,et al.  Computer-based technique for cell aggregation analysis and cell aggregation in in vitro chondrogenesis. , 1997, Cytometry.

[28]  E. Papoutsakis,et al.  Damage mechanisms of suspended animal cells in agitated bioreactors with and without bubble entrainment , 1990, Biotechnology and bioengineering.

[29]  O. Levenspiel Chemical Reaction Engineering , 1972 .

[30]  R Langer,et al.  Effects of mixing intensity on tissue-engineered cartilage. , 2001, Biotechnology and bioengineering.

[31]  J. Abbott,et al.  THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS , 1969, The Journal of experimental medicine.