PMID- 15264307 OWN - NLM STAT- MEDLINE DCOM- 20051207 LR - 20200930 IS - 1552-4973 (Print) IS - 1552-4973 (Linking) VI - 70 IP - 2 DP - 2004 Aug 15 TI - Osteoblast-like cell response to bioactive composites-surface-topography and composition effects. PG - 250-61 AB - Two bioactive composites, containing 40 vol % filler in high-density polyethylene (HDPE), were investigated to examine the effects of different filler compositions and different surface patterning. The first composite, known as HAPEX, consists of hydroxyapatite within HDPE, and the second composite, known as AWPEX, consists of glass-ceramic apatite-wollastonite in HDPE. Surface topography effects at 5-50 and 100-150 microm were explored, with cell morphology analyzed with the use of scanning electron microscopy and confocal laser scanning microscopy (CLSM). Biochemical assays of adenosine triphosphate and alkaline phosphatase were used to analyze osteoblast-like cell proliferation and differentiation. For both composites, cell alignment was seen along grooves, pillars, and wells, with preferential cell attachment to ceramic particles within the polymer matrices. HAPEX showed significantly increased cell proliferation over AWPEX (P < 0.005). However, greater cell differentiation occurred for AWPEX over HAPEX (P < 0.005). Polishing significantly increased osteoblast-like cell response over as-cut samples, but surface-topography changes above 50 microm had no consistent effect. Smaller-scale features also showed no significant trend in terms of cell proliferation, but did show significant differences in cell differentiation (P < 0.05). CLSM imaging of actin and vinculin localization within cells showed the greatest change in comparison to polished surface controls for cells cultured on samples with surface features below 50 microm. The fact that similar observations were made for both HAPEX and AWPEX indicated that, for these experiments, the effects of surface topography more strongly influenced cell response than chemical composition. CI - Copyright 2004 Wiley Periodicals, Inc. FAU - Rea, Susan M AU - Rea SM AD - Department of Materials Science and Metallurgy, University of Cambridge, Pembroke Street, Cambridge CB2 3QZ, England. smr31@cam.ac.uk FAU - Brooks, Roger A AU - Brooks RA FAU - Schneider, Andreas AU - Schneider A FAU - Best, Serena M AU - Best SM FAU - Bonfield, William AU - Bonfield W LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Biomed Mater Res B Appl Biomater JT - Journal of biomedical materials research. Part B, Applied biomaterials JID - 101234238 RN - 0 (Apatites) RN - 0 (Bone Substitutes) RN - 0 (Calcium Compounds) RN - 0 (Silicates) RN - 8L70Q75FXE (Adenosine Triphosphate) RN - 9002-88-4 (Polyethylene) RN - EC 3.1.3.1 (Alkaline Phosphatase) RN - S4255P4G5M (calcium silicate) SB - IM MH - Adenosine Triphosphate/metabolism MH - Alkaline Phosphatase/metabolism MH - Apatites/*pharmacology MH - Bone Substitutes/*pharmacology MH - Calcium Compounds/*pharmacology MH - Cell Differentiation/drug effects MH - Cell Proliferation/drug effects MH - Cells, Cultured MH - Humans MH - Microscopy, Confocal MH - Microscopy, Electron, Scanning MH - Osteoblasts/*cytology/drug effects MH - Polyethylene/*pharmacology MH - Silicates/*pharmacology MH - Surface Properties EDAT- 2004/07/21 05:00 MHDA- 2005/12/13 09:00 CRDT- 2004/07/21 05:00 PHST- 2004/07/21 05:00 [pubmed] PHST- 2005/12/13 09:00 [medline] PHST- 2004/07/21 05:00 [entrez] AID - 10.1002/jbm.b.30039 [doi] PST - ppublish SO - J Biomed Mater Res B Appl Biomater. 2004 Aug 15;70(2):250-61. doi: 10.1002/jbm.b.30039.