Effects of the architecture of tissue engineering scaffolds on cell seeding and culturing.

The advance of rapid prototyping techniques has significantly improved control over the pore network architecture of tissue engineering scaffolds. In this work, we have assessed the influence of scaffold pore architecture on cell seeding and static culturing, by comparing a computer designed gyroid architecture fabricated by stereolithography with a random pore architecture resulting from salt leaching. The scaffold types showed comparable porosity and pore size values, but the gyroid type showed a more than 10-fold higher permeability due to the absence of size-limiting pore interconnections. The higher permeability significantly improved the wetting properties of the hydrophobic scaffolds and increased the settling speed of cells upon static seeding of immortalised mesenchymal stem cells. After dynamic seeding followed by 5 days of static culture gyroid scaffolds showed large cell populations in the centre of the scaffold, while salt-leached scaffolds were covered with a cell sheet on the outside and no cells were found in the scaffold centre. It was shown that interconnectivity of the pores and permeability of the scaffold prolonged the time of static culture before overgrowth of cells at the scaffold periphery occurred. Furthermore, novel scaffold designs are proposed to further improve the transport of oxygen and nutrients throughout the scaffolds and to create tissue engineering grafts with a designed, pre-fabricated vasculature.

[1]  C. V. van Blitterswijk,et al.  In vitro and in vivo bioluminescent imaging of hypoxia in tissue-engineered grafts. , 2010, Tissue engineering. Part C, Methods.

[2]  Jean-Jacques Clair Stereolithography and the biomedical engineering , 1996 .

[3]  Ivan Martin,et al.  In vitro differentiation of chick embryo bone marrow stromal cells into cartilaginous and bone‐like tissues , 1998, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[4]  J. Jukes,et al.  Critical Steps toward a tissue-engineered cartilage implant using embryonic stem cells. , 2008, Tissue engineering. Part A.

[5]  Jan Feijen,et al.  A poly(D,L-lactide) resin for the preparation of tissue engineering scaffolds by stereolithography. , 2009, Biomaterials.

[6]  A. Leusink,et al.  In vivo evaluation of highly macroporous ceramic scaffolds for bone tissue engineering. , 2009, Journal of biomedical materials research. Part A.

[7]  P. Rouxhet,et al.  Competitive adsorption of proteins: key of the relationship between substratum surface properties and adhesion of epithelial cells. , 1999, Biomaterials.

[8]  A. Schoen Infinite periodic minimal surfaces without self-intersections , 1970 .

[9]  W. Mutschler,et al.  Hypoxia in static and dynamic 3D culture systems for tissue engineering of bone. , 2008, Tissue engineering. Part A.

[10]  Lorenzo Moroni,et al.  3D Fiber‐Deposited Electrospun Integrated Scaffolds Enhance Cartilage Tissue Formation , 2008 .

[11]  G. Vunjak‐Novakovic,et al.  Culture of organized cell communities. , 1998, Advanced drug delivery reviews.

[12]  Shangtian Yang,et al.  Effects of Filtration Seeding on Cell Density, Spatial Distribution, and Proliferation in Nonwoven Fibrous Matrices , 2001, Biotechnology progress.

[13]  R. Mann,et al.  Human Physiology , 1839, Nature.

[14]  Young Ha Kim,et al.  New technique of seeding chondrocytes into microporous poly(L-lactide-co-epsilon-caprolactone) sponge by cyclic compression force-induced suction. , 2006, Tissue engineering.

[15]  J. Feijen,et al.  Physical properties of high molecular weight 1,3-trimethylene carbonate and D,L-lactide copolymers , 2003, Journal of materials science. Materials in medicine.

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

[17]  Robert Langer,et al.  Preparation and characterization of poly(l-lactic acid) foams , 1994 .

[18]  H. Schwarz Gesammelte mathematische Abhandlungen , 1970 .

[19]  J Tramper,et al.  The effect of PEGT/PBT scaffold architecture on oxygen gradients in tissue engineered cartilaginous constructs. , 2004, Biomaterials.

[20]  R. Langer,et al.  Wetting of poly(L-lactic acid) and poly(DL-lactic-co-glycolic acid) foams for tissue culture. , 1994, Biomaterials.

[21]  D. Kohane,et al.  Engineering vascularized skeletal muscle tissue , 2005, Nature Biotechnology.

[22]  D. Wendt,et al.  Uniform tissues engineered by seeding and culturing cells in 3D scaffolds under perfusion at defined oxygen tensions. , 2006, Biorheology.

[23]  E. Sachlos,et al.  ON THE APPLICATION OF SOLID FREEFORM FABRICATION TECHNOLOGY TO THE PRODUCTION OF TISSUE ENGINEERING SCAFFOLDS , 2022 .

[24]  K. Shakesheff,et al.  Seeding cells into needled felt scaffolds for tissue engineering applications. , 2003, Journal of biomedical materials research. Part A.

[25]  M J Yaszemski,et al.  Ectopic bone formation by marrow stromal osteoblast transplantation using poly(DL-lactic-co-glycolic acid) foams implanted into the rat mesentery. , 1997, Journal of biomedical materials research.

[26]  D. Wendt,et al.  Oscillating perfusion of cell suspensions through three‐dimensional scaffolds enhances cell seeding efficiency and uniformity , 2003, Biotechnology and bioengineering.

[27]  D J Mooney,et al.  Optimizing seeding and culture methods to engineer smooth muscle tissue on biodegradable polymer matrices. , 1998, Biotechnology and bioengineering.

[28]  K. Nose,et al.  HIF-1-dependent VEGF reporter gene assay by a stable transformant of CHO cells. , 2003, Biological & pharmaceutical bulletin.