Effect of functionalized polycaprolactone on the behaviour of murine preosteoblasts

Biomaterials

Volumn 31, Issue 25, 2010, Pages 6468-6476

  Drevelle, Olivier ^a   Bergeron, Eric ^a   Senta, Helena ^a   Lauzon, Marc Antoine ^a   Roux, Sophie ^b   Grenier, Guillaume ^a,b   Faucheux, Nathalie ^a,b  

^a UNIVERSITÉ DE SHERBROOKE   (Canada)

^b Centre Hospitalier Universitaire de Sherbrooke   (Canada)

Author keywords

Actin; Cell signalling; RGD peptides; Vinculin

Indexed keywords

ALKALINITY; BIOMATERIALS; BODY FLUIDS; BONE; CELL SIGNALING; CELLS; CYTOLOGY; HYDROLYSIS; HYDROPHILICITY; PEPTIDES; RECOMBINANT PROTEINS; SODIUM HYDROXIDE; X RAY PHOTOELECTRON SPECTROSCOPY;

ACTIN; CARBOXYLIC ACID GROUPS; CELL SIGNALLING; CYTOSKELETAL ORGANIZATION; PEPTIDE IMMOBILIZATION; RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2 (RHBMP-2); RGD PEPTIDE; VINCULIN;

POLYCAPROLACTONE;

ARGINYLGLYCYLASPARTIC ACID; CARBOXYLIC ACID; FIBRONECTIN; FOCAL ADHESION KINASE; POLYCAPROLACTONE; RECOMBINANT BONE MORPHOGENETIC PROTEIN 2; SIALOPROTEIN; SMAD1 PROTEIN; SMAD5 PROTEIN; SMAD8 PROTEIN; SODIUM HYDROXIDE; VITRONECTIN; ARGINYL-GLYCYL-GLUTAMIC ACID; BIOMATERIAL; BONE MORPHOGENETIC PROTEIN; BONE MORPHOGENETIC PROTEIN 2; OLIGOPEPTIDE; POLYESTER; RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN-2; RECOMBINANT PROTEIN; SMAD PROTEIN; TRANSFORMING GROWTH FACTOR BETA;

ADSORPTION; ANIMAL CELL; ARTICLE; CELL ADHESION; CELL FUNCTION; CELL SPREADING; CHEMICAL COMPOSITION; CONTROLLED STUDY; CYTOSKELETON; FILM; HYDROLYSIS; HYDROPHILICITY; MOLECULAR WEIGHT; MOUSE; NONHUMAN; OSTEOBLAST; PRIORITY JOURNAL; PROTEIN IMMOBILIZATION; PROTEIN PHOSPHORYLATION; ROUGHNESS; SIGNAL TRANSDUCTION; SURFACE PROPERTY; WETTABILITY; X RAY PHOTOELECTRON SPECTROSCOPY; 3T3 CELL LINE; ANIMAL; CHEMISTRY; CYTOLOGY; HUMAN; METABOLISM; ULTRASTRUCTURE;

MURINAE;

3T3 CELLS; ADSORPTION; ANIMALS; BIOCOMPATIBLE MATERIALS; BONE MORPHOGENETIC PROTEIN 2; BONE MORPHOGENETIC PROTEINS; CYTOSKELETON; FIBRONECTINS; FOCAL ADHESION PROTEIN-TYROSINE KINASES; HUMANS; MICE; OLIGOPEPTIDES; OSTEOBLASTS; POLYESTERS; RECOMBINANT PROTEINS; SMAD PROTEINS; TRANSFORMING GROWTH FACTOR BETA; VITRONECTIN; WETTABILITY;

EID: 77953959567     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2010.05.010     Document Type: Article

References (37)

1. Puleo D.A., Nancy A. Understanding and controlling the bone-implant interface. Biomaterials 1999, 20:2311-2321.
2. Marquis M.E., Lord E., Bergeron E., Drevelle O., Park H., Cabana F., et al. Bone cells-biomaterials interactions. Front Biosci 2009, 14:1023-1067.
3. Pierschbacher M.D., Ruoslahti E. Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule. Nature 1984, 309:30-33.
4. Rezania A., Healy K.E. Biomimetic peptide surfaces that regulate adhesion, spreading, cytoskeletal organization, and mineralization of the matrix deposited by osteoblast-like cells. Biotechnol Prog 1999, 15:19-32.
5. Shin H., Zygouraskis K., Farach-Carson M.C., Yaszemski M.J., Mikos A.G. Attachment, proliferation and migration of marrow stromal osteoblasts cultured on biomimetic hydrogels modified with an osteopontin-derived peptide. Biomaterials 2004, 25:895-906.
6. Barber T.A., Gamble L.J., Castner D.G., Healy K.E. In vitro characterization of peptide-modified p(AAm-co-EG/AAc) IPN-coated titanium implants. J Orthop Res 2006, 24:1366-1376.
7. Hersel U., Dahmen C., Kessler H. RGD modified polymers: biomaterials for stimulated cell adhesion and beyond. Biomaterials 2003, 24:4385-4415.
8. Marquis M.E., Lord E., Bergeron E., Bourgoin L., Faucheux N. Short-term effects of adhesion peptides on the responses of preosteoblasts to pBMP-9. Biomaterials 2008, 29:1005-1016.
9. Ferris D.M., Moodie G.D., Dimond P.M., Giorani C.W.D., Ehrlich M.G., Valentini R.F. RGD-coated titanium implants stimulate increased bone formation in vivo. Biomaterials 1999, 20:2323-2331.
10. Hennessy K.M., Clem W.C., Phipps M.C., Sawyer A.A., Shaikh F.M., Bellis S.L. The effect of RGD peptides on osseointegration of hydroxyapatite biomaterials. Biomaterials 2008, 29:3075-3083.
11. Liao S., Chan C.K., Ramakrishna S. Stem cells and biomimetic materials strategies for tissue engineering. Mater Sci Eng C 2008, 28:1189-1202.
12. Marletta G., Ciapetti G., Satriano C., Pagani S., Baldini N. The effect of irradiation modification and RGD sequence adsorption on the response of human osteoblasts to polycaprolactone. Biomaterials 2005, 26:4793-4804.
13. Zhang H., Hollister S.J. Comparison of bone marrow stromal cell behaviors on poly (caprolactone) with or without surface modification: studies on cell adhesion, survival and proliferation. J Biomater Sci 2009, 20:1975-1993.
14. Karakecili A., Satriano C., Gumusderelioglu M., Marletta G. Relationship between the fibroblastic behaviour and surface properties of RGD-immobilized PCL membranes. J Mater Sci Mater Med 2007, 18:317-319.
15. He X., Ma J., Jabbari E. Effect of grafting RGD and BMP-2 protein derived peptides to a hydrogel substrate on osteogenic differentiation of marrow stromal cells. Langmuir 2008, 24:12508-12516.
16. Lavery K., Swain P., Falb D., Alaoui-Ismaili M.H. BMP-2/4 and BMP-6/7 differentially utilize cell surface receptors to induce osteoblastic differentiation of human bone marrow-derived mesenchymal stem cells. J Biol Chem 2008, 283:20948-20958.
17. Burkus J.K., Heim S.E., Gornet M.F., Zdeblick T.A. The effectiveness of rhBMP-2 in replacing autograft: an integrated analysis of three human spine studies. Orthopedics 2004, 27:723-728.
18. Sun H., Önneby S. Facile polyester surface functionalization via hydrolysis and cell-recognizing peptide attachment. Polym Int 2006, 55:1336-1340.
19. Ng K.W., Hutmacher D.W., Schantz J.T., Seng C., Too H.P., Lim T.C., et al. Evaluation of ultra-thin poly(e{open}-caprolactone) films for tissue-engineered skin. Tissue Eng 2001, 7:441-455.
20. Vance R.J., Miller D.C., Thapa A., Haberstroh K.M., Webster T.J. Decreased fibroblast cell density on chemically degraded poly-lactic-co-glycolic acid, polyurethane, and polycaprolactone. Biomaterials 2004, 25:2095-2103.
21. Rouxhet L., Duhoux F., Borecky O., Legras R., Schneider Y.J. Adsorption of albumin, collagen, and fibronectin on the surface of poly(hydroxybutyrate-hydroxyvalerate) (PHB/HV) and of poly(e{open}-caprolactone) (PCL) films modified by alkaline hydrolysis and of poly(ethylene terephtalate) (PET) track-etched membranes. J Biomater Sci Polym Ed 1998, 9:1279-1304.
22. Tan P.S., Teoh S.H. Effect of stiffness of polycaprolactone (PCL) membrane on cell proliferation. Mater Sci Eng C 2007, 27:304-308.
23. Khor H.L., Ng K.W., Htay A.S., Schantz J.T., Teoh S.H., Hutmacher D.W. Preliminary study of a polycaprolactone membrane utilized as epidermal substrate. J Mater Sci Mater Med 2003, 14:113-120.
24. Collier T.O., Jenney C.R., Defife K.M., Anderson J.M. Protein adsorption on chemically modified surfaces. Biomed Sci Instrum 1997, 33:178-183.
25. Schneider G., Burridge K. Formation of focal adhesions by osteoblasts adhering to different substrata. Exp Cell Res 1994, 214:264-269.
26. Hayman E.G., Pierschbacher M.D., Suzuki S., Ruoslahti E. Vitronectin-a major cell attachment-promoting protein in fetal bovine serum. Exp Cell Res 1985, 160:245-258.
27. Steele J.G., Dalton B.A., Johnson G., Underwood P.A. Adsorption of fibronectin and vitronectin onto Primaria™ and tissue culture polystyrene and relationship to the mechanism of initial attachment of human vein endothelial cells and BHK-21 fibroblasts. Biomaterials 1995, 16:1057-1067.
28. Faucheux N., Schweiss R., Lutzow K., Werner C., Groth T. Self-assembled monolayers with different terminating groups as model substrates for cell adhesion studies. Biomaterials 2004, 25:2721-2730.
29. Zhang H., Lin C.Y., Hollister S.J. The interaction between bone marrow stromal cells and RGD-modified three-dimensional porous polycaprolactone scaffolds. Biomaterials 2009, 30:4063-4069.
30. Rezania A., Thomas C.H., Branger A.B., Waters C.M., Healy K.E. The detachment strength and morphology of bone cells contacting materials modified with a peptide sequence found within bone sialoprotein. J Biomed Mater Res 1997, 37:9-19.
31. Rapuano B.E., Wu C., MacDonald D.E. Osteoblast-like cell adhesion to bone sialoprotein peptides. J Orthop Res 2004, 22:353-361.
32. Wozniak M.A., Modzelewska K., Kwong L., Keely P.J. Focal adhesion regulation of cell behavior. Biochim Biophys Acta 2004, 1692:103-119.
33. src. Mol Cell Bio 1994, 14:1680-1688.
34. Frisch S.M., Vuori K., Ruoslahti E., Chan-Hui P.Y. Control of adhesion-dependent cell survival by focal adhesion kinase. J Cell Biol 1996, 134:793-799.
35. Tamura Y., Takeuchi Y., Suzawa M., Fukumoto S., Kato M., Miyazono K., et al. Focal adhesion kinase activity is required for bone morphogenetic protein-Smad1 signaling and osteoblastic differentiation in murine MC3T3-E1 cells. J Bone Miner Res 2001, 16:1772-1779.
36. Miyazono K. Signal transduction by bone morphogenetic protein receptors: functional roles of Smad proteins. Bone 1999, 25:91-93.
37. vβ integrins play an essential role in BMP-2 induction of osteoblast differentiation. J Bone Miner Res 2005, 20:330-340.