Surface immobilization of MEPE peptide onto HA/β-TCP ceramic particles enhances bone regeneration and remodeling†
Bodhraj Acharya
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Search for more papers by this authorSo-Young Chun
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Joint Institute for Regenerative Medicine, Kyungpook National University Hospital, Daegu 700-412, Korea
Search for more papers by this authorShin-Yoon Kim
Department of Orthopaedic Surgery, School of Medicine, Kyungpook National University, Daegu 700-412, Korea
Search for more papers by this authorCheil Moon
Department of Brain Science, Daegu Gyeongbuk Institute of Science & Technology, Daegu 711-873, Korea
Search for more papers by this authorHong-In Shin
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Search for more papers by this authorCorresponding Author
Eui Kyun Park
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, KoreaSearch for more papers by this authorBodhraj Acharya
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Search for more papers by this authorSo-Young Chun
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Joint Institute for Regenerative Medicine, Kyungpook National University Hospital, Daegu 700-412, Korea
Search for more papers by this authorShin-Yoon Kim
Department of Orthopaedic Surgery, School of Medicine, Kyungpook National University, Daegu 700-412, Korea
Search for more papers by this authorCheil Moon
Department of Brain Science, Daegu Gyeongbuk Institute of Science & Technology, Daegu 711-873, Korea
Search for more papers by this authorHong-In Shin
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Search for more papers by this authorCorresponding Author
Eui Kyun Park
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, Korea
Department of Pathology and Regenerative Medicine, School of Dentistry, Institute for Hard Tissue and Bio-Tooth Regeneration, Kyungpook National University, Daegu 700-412, KoreaSearch for more papers by this authorHow to cite this article: Acharya B, Chun S-Y, Kim S-Y, Moon C, Shin H-I, Park EK. 2012. Surface immobilization of MEPE peptide onto HA/β-TCP ceramic particles enhances bone regeneration and remodeling. J Biomed Mater Res Part B 2012:100B:841–849.
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. J Biomed Mater Res Part B: Appl Biomater, 2012.
Supporting Information
Additional Supporting Information may be found in the online version of this article.
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JBM_32648_sm_SuppFig1.tif1.3 MB | Supporting Information Figure 1 |
JBM_32648_sm_SuppFig2.tif1.8 MB | Supporting Information Figure 2 |
JBM_32648_sm_SuppFig3.tif1.4 MB | Supporting Information Figure 3 |
JBM_32648_sm_SuppFig4.tif1.3 MB | Supporting Information Figure 4 |
JBM_32648_sm_SuppFig5.tif17.6 MB | Supporting Information Figure 5 |
JBM_32648_sm_SuppFig6.tif8 MB | Supporting Information Figure 6 |
JBM_32648_sm_SuppFig7.tif6.5 MB | Supporting Information Figure 7 |
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