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Surface immobilization of MEPE peptide onto HA/ss-TCP ceramic particles enhances bone regeneration and remodeling
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- Title
- Surface immobilization of MEPE peptide onto HA/ss-TCP ceramic particles enhances bone regeneration and remodeling
- DGIST Authors
- Moon, C[Moon, Cheil]
- Issued Date
- 2012-04
- Citation
- Acharya, B[Acharya, Bodhraj]. (2012-04). Surface immobilization of MEPE peptide onto HA/ss-TCP ceramic particles enhances bone regeneration and remodeling. doi: 10.1002/jbm.b.32648
- Type
- Article
- Article Type
- Article
- Subject
- Acid Phosphatase Tartrate Resistant Isoenzyme ; Animal Experiment ; Animal Model ; Animals ; Bioactive Peptides ; Bone ; Bone Area ; Bone Defect ; Bone Mineralization ; Bone Regeneration ; Bone Remodeling ; Calcium Phosphate ; Calcium Phosphate Ceramic ; Calcium Phosphate Ceramics ; Calcium Phosphates ; Calvaria ; Calvarial Defects ; Carboxy Terminal Sequence ; Cell Differentiation ; Cells, Cultured ; Ceramic Particle ; Covalent Bond ; Disease Models, Animal ; Durapatite ; Extracellular ; Extracellular Matrix Proteins ; FT-IR ; Glycoproteins ; Hematopoietic Stem Cell ; Human ; Human Cell ; Humans ; Hydroxyapatite ; Immobilized Proteins ; In-Situ ; Infrared Spectroscopy ; Male ; Matrix Extracellular Phosphoglycoprotein ; MEPE and Bone Marrow Stem Cell ; Mice ; Mice, Inbred ICR ; Micro-Computed Tomography ; Micro CT ; Mouse ; Non-Human ; Osteoblast ; Osteoblast Differentiation ; Osteoblasts ; Osteoclast ; Osteoclasts ; Osteogenic Potential ; Peptide Immobilization ; Peptides ; Phosphatases ; Phosphoproteins ; Protein Immobilization ; Scaffolds (Biology) ; Skull Fractures ; Stem Cells ; Surface Immobilization ; Surface Modification ; Surface Treatment ; Tri-Calcium Phosphates ; X Ray Photoelectron Spectroscopy
- ISSN
- 1552-4973
- Abstract
-
Calcium phosphate ceramics have been widely used as scaffolds for bone regeneration. Here, to improve the osteogenic potential of hydroxyapatite/ β-tricalcium phosphate (HA/β-TCP) and to apply the bioactive peptide in situ, matrix extracellular phosphoglycoprotein (MEPE) peptide, which has been shown to stimulate osteoblast differentiation, was covalently and directionally immobilized on HA/β-TCP particles. The free-hydroxyl groups on the surface of the HA/β-TCP particles were sequentially conjugated with APTES, PEG-(SS) 2, and the synthetic MEPE peptide. Using FTIR and XPS, immobilization of the MEPE peptide on the HA/β-TCP was confirmed. Implantation of the MEPE peptide-immobilized HA/β-TCP into calvarial defect and subsequent analyses using a micro CT and histology showed significant bone regeneration and increased bone area (9.89-fold) as compared to that of unmodified HA/β-TCP. Moreover, tartrate-resistant acid phosphatase-positive osteoclasts were observed in regenerated bone by the MEPE peptide-immobilized HA/β-TCP, indicating that the bones newly formed by the MEPE peptide-immobilized HA/β-TCP are actively remodeled by osteoclasts. Therefore, our data demonstrate that MEPE peptide immobilization onto the HA/β-TCP surface stimulates bone regeneration associated with physiological bone remodeling. © 2012 WILEY PERIODICALS, INC.
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- Publisher
- Wiley Blackwell
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