Differential effects of designed scaffold permeability on chondrogenesis by chondrocytes and bone marrow stromal cells

Biomaterials

Volumn 31, Issue 2, 2010, Pages 279-287

  Kemppainen, Jessica M ^a   Hollister, Scott J ^a,b  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

Bone marrow stromal cell; Cartilage tissue engineering; Chondrocyte; Polycaprolactone; Scaffold

Indexed keywords

BONE MARROW STROMAL CELL; BONE MARROW STROMAL CELLS; CAPROLACTONE; CARTILAGE REGENERATION; CARTILAGE TISSUE ENGINEERING; CELL DIFFERENTIATION; CELLULAR DIFFERENTIATION; CHONDROCYTE; CHONDROCYTES; CHONDROGENESIS; CHONDROGENIC; CHONDROGENIC POTENTIAL; DIFFERENTIAL EFFECT; HIGH PERMEABILITY; IN-VITRO; MATERIAL DESIGNS; MATRIX; PHYSICAL DESIGN; PRIMARY CHONDROCYTES; PROGENITOR CELL;

BODY FLUIDS; BONE; CAPILLARITY; CARTILAGE; COLLAGEN; DESIGN; GENE EXPRESSION; LIGAMENTS; POLYCAPROLACTONE; TISSUE ENGINEERING;

SCAFFOLDS;

AGGRECAN; BIOMATERIAL; COLLAGEN TYPE 1; COLLAGEN TYPE 2; POLYCAPROLACTONE; TISSUE SCAFFOLD;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BONE MARROW CELL; CARTILAGE CELL; CARTILAGE MATRIX; CELL ACTIVITY; CELL DIFFERENTIATION; CELL LINEAGE; CHONDROGENESIS; CONTROLLED STUDY; GENE EXPRESSION; NONHUMAN; PERMEABILITY; PRIORITY JOURNAL; STROMA CELL;

AGGRECANS; ANIMALS; BONE MARROW CELLS; CHONDROCYTES; CHONDROGENESIS; COLLAGEN; DNA; PERMEABILITY; STAINING AND LABELING; STROMAL CELLS; SURFACE PROPERTIES; SWINE; SWINE, MINIATURE; TISSUE SCAFFOLDS;

EID: 70350728396     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2009.09.041     Document Type: Article

References (40)

1. Li S.H., de Wijn J.R., Layrolle P., and de Groot K. Accurate geometric characterization of macroporous scaffold of tissue engineering. Bioceramics 240-2 (2003) 541-545
2. Maroudas. Permeability of articular cartilage. Nature 219 (1968) 1260
3. Karande T.S., Ong J.L., and Agrawal C.M. Diffusion in musculoskeletal tissue engineering scaffolds: design issues related to porosity, permeability, architecture, and nutrient mixing. Ann Biomed Eng 32 (2004) 1728-1743
4. Clark C.C., Tolin B.S., and Brighton C.T. The effect of oxygen tension on proteoglycan synthesis and aggregation in mammalian growth plate chondrocytes. J Orthop Res 9 (1991) 477-484
5. Malda J., van den Brink P., Meeuwse P., Grojec M., Martens D.E., Tramper J., et al. Effect of oxygen tension on adult articular chondrocytes in microcarrier bioreactor culture. Tissue Eng 10 (2004) 987-994
6. Schneider N., Mouithys-Mickalad A., Lejeune J.P., Duyckaerts C., Sluse F., Deby-Dupont G., et al. Oxygen consumption of equine articular chondrocytes: influence of applied oxygen tension and glucose concentration during culture. Cell Biol Int 31 (2007) 878-886
7. Henrotin Y.E., Bruckner P., and Pujol J.P. The role of reactive oxygen species in homeostasis and degradation of cartilage. Osteoarthritis Cartilage 11 (2003) 747-755
8. Yoo J.U., Barthel T.S., Nishimura K., Solchaga L., Caplan A.I., Goldberg V.M., et al. The chondrogenic potential of human bone-marrow-derived mesenchymal progenitor cells. J Bone Joint Surg Am 80 (1998) 1745-1757
9. Bhardwaj T., Pilliar R.M., Grynpas M.D., and Kandel R.A. Effect of material geometry on cartilagenous tissue formation in vitro. J Biomed Mater Res 57 (2001) 190-199
10. Malda J., Martens D.E., Tramper J., van Blitterswijk C.A., and Riesle J. Cartilage tissue engineering: controversy in the effect of oxygen. Crit Rev Biotechnol 23 (2003) 175-194
11. Malda J., van Blitterswijk C.A., van Geffen M., Martens D.E., Tramper J., and Riesle J. Low oxygen tension stimulates the redifferentiation of dedifferentiated adult human nasal chondrocytes. Osteoarthritis Cartilage 12 (2004) 306-313
12. Kurz B., Domm C., Jin M., Sellckau R., and Schunke M. Tissue engineering of articular cartilage under the influence of collagen I/III membranes and low oxygen tension. Tissue Eng 10 (2004) 1277-1286
13. Murphy C.L., and Sambanis A. Effect of oxygen tension and alginate encapsulation on restoration of the differentiated phenotype of passaged chondrocytes. Tissue Eng 7 (2001) 791-803
14. Murphy C.L., and Sambanis A. Effect of oxygen tension on chondrocyte extracellular matrix accumulation. Connect Tissue Res 42 (2001) 87-96
15. Domm C., Schunke M., Christesen K., and Kurz B. Redifferentiation of dedifferentiated bovine articular chondrocytes in alginate culture under low oxygen tension. Osteoarthritis Cartilage 10 (2002) 13-22
16. Hansen U., Schunke M., Domm C., Ioannidis N., Hassenpflug J., Gehrke T., et al. Combination of reduced oxygen tension and intermittent hydrostatic pressure: a useful tool in articular cartilage tissue engineering. J Biomech 34 (2001) 941-949
17. Nagel-Heyer S., Goepfert C., Adamietz P., Meenen N.M., and Portner R. Cultivation of three-dimensional cartilage-carrier-constructs under reduced oxygen tension. J Biotechnol 121 (2006) 486-497
18. Saini S., and Wick T.M. Effect of low oxygen tension on tissue-engineered cartilage construct development in the concentric cylinder bioreactor. Tissue Eng 10 (2004) 825-832
19. Schneider N., Lejeune J.P., Deby C., Deby-Dupont G.P., and Serteyn D. Viability of equine articular chondrocytes in alginate beads exposed to different oxygen tensions. Vet J 168 (2004) 167-173
20. Wernike E., Li Z., Alini M., and Grad S. Effect of reduced oxygen tension and long-term mechanical stimulation on chondrocyte-polymer constructs. Cell Tissue Res 331 (2008) 473-483
21. Pawelek J.M. Effects of thyroxine and low oxygen tension on chondrogenic expression in cell culture. Dev Biol 19 (1969) 52-72
22. Grimshaw M.J., and Mason R.M. Modulation of bovine articular chondrocyte gene expression in vitro by oxygen tension. Osteoarthritis Cartilage 9 (2001) 357-364
23. Grimshaw M.J., and Mason R.M. Bovine articular chondrocyte function in vitro depends upon oxygen tension. Osteoarthritis Cartilage 8 (2000) 386-392
24. Kanichai M., Ferguson D., Prendergast P.J., and Campbell V.A. Hypoxia promotes chondrogenesis in rat mesenchymal stem cells: a role for AKT and hypoxia-inducible factor (HIF)-1alpha. J Cell Physiol 216 (2008) 708-715
25. Robins J.C., Akeno N., Mukherjee A., Dalal R.R., Aronow B.J., Koopman P., et al. Hypoxia induces chondrocyte-specific gene expression in mesenchymal cells in association with transcriptional activation of Sox9. Bone 37 (2005) 313-322
26. Hollister S.J., and Lin C.Y. Computational design of tissue engineering scaffolds. Comput Methods Appl Mech Eng 196 (2007) 2991-2998
27. Li J., and Mak A.F. Hydraulic permeability of polyglycolic acid scaffolds as a function of biomaterial degradation. J Biomater Appl 19 (2005) 253-266
28. Farndale R.W., Buttle D.J., and Barrett A.J. Improved quantitation and discrimination of sulphated glycosaminoglycans by use of dimethylmethylene blue. Biochim Biophys Acta 883 (1986) 173-177
29. Goldberg V.M., and Caplan A.I. Orthopedic tissue engineering: basic science and practice (2004), Marcel Dekker, New York
30. Barlic A., Drobnic M., Malicev E., and Kregar-Velikonja N. Quantitative analysis of gene expression in human articular chondrocytes assigned for autologous implantation. J Orthop Res (2008)
31. Schulze-Tanzil G., Muller R.D., Kohl B., Schneider N., Ertel W., Ipaktchi K., et al. Differing in vitro biology of equine, ovine, porcine and human articular chondrocytes derived from the knee joint: an immunomorphological study. Histochem Cell Biol 131 (2009) 219-229
32. Martin I., Jakob M., Schafer D., Dick W., Spagnoli G., and Heberer M. Quantitative analysis of gene expression in human articular cartilage from normal and osteoarthritic joints. Osteoarthritis Cartilage 9 (2001) 112-118
33. Hall B.K. Bones and cartilage: developmental and evolutionary skeletal biology (2005), Elsevier Academic Press, Australia; San Diego, CA
34. Lund-Olesen K. Oxygen tension in synovial fluids. Arthritis Rheum 13 (1970) 769-776
35. Falchuk K.H., Goetzl E.J., and Kulka J.P. Respiratory gases of synovial fluids. An approach to synovial tissue circulatory-metabolic imbalance in rheumatoid arthritis. Am J Med 49 (1970) 223-231
36. Woodhouse C.F. An instrument for the measurement of oxygen tension in bone - a preliminary report. J Bone Joint Surg Am 43 (1961) 819-828
37. Reddi A.H., and Huggins C.B. Influence of geometry of transplanted tooth and bone on transformation of fibroblasts. Proc Soc Exp Biol Med 143 (1973) 634-637
38. Yoon D.M., Hawkins E.C., Francke-Carroll S., and Fisher J.P. Effect of construct properties on encapsulated chondrocyte expression of insulin-like growth factor-1. Biomaterials 28 (2007) 299-306
39. Nehrer S., Breinan H.A., Ramappa A., Young G., Shortkroff S., Louie L.K., et al. Matrix collagen type and pore size influence behaviour of seeded canine chondrocytes. Biomaterials 18 (1997) 769-776
40. Kuboki Y., Jin Q., Kikuchi M., Mamood J., and Takita H. Geometry of artificial ECM: sizes of pores controlling phenotype expression in BMP-induced osteogenesis and chondrogenesis. Connect Tissue Res 43 (2002) 529-534