論文 - 詳細
| RRC ID | 65530 |
|---|---|
| 著者 | Fujioka-Kobayashi M, Schaler B, Shirakata Y, Nakamura T, Noguchi K, Zhang Y, Miron RJ. |
| タイトル | Comparison of Two Porcine Collagen Membranes Combined with rhBMP-2 and rhBMP-9 on Osteoblast Behavior In Vitro. |
| ジャーナル | Int J Oral Maxillofac Implants |
| Abstract |
PURPOSE:To investigate the bone-inducing properties of two types of collagen membranes in combination with recombinant human bone morphogenetic protein (rhBMP)-2 and rhBMP-9 on osteoblast behavior. MATERIALS AND METHODS:Porcine pericardium collagen membranes (PPCM) and porcine dermis-derived collagen membranes (PDCM) were coated with either rhBMP-2 or rhBMP-9. The adsorption and release abilities were first investigated via enzyme-linked immunosorbent assay up to 10 days. Moreover, murine bone stromal ST2 cell adhesion, proliferation, and osteoblast differentiation were assessed by MTS assay; real-time polymerase chain reaction for genes encoding runt-related transcription factor 2 (Runx2); alkaline phosphatase (ALP); and osteocalcin, ALP assay, and alizarin red staining. RESULTS:Both rhBMP-2 and rhBMP-9 adsorbed to collagen membranes and were gradually released over time up to 10 days. PPCM showed significantly less cell attachment, whereas PDCM demonstrated comparable cell attachment with the control tissue culture plastic at 8 hours. While both rhBMPs were shown not to affect cell proliferation, collagen membranes combined with rhBMP-9 significantly increased ALP activity at 7 days and ALP mRNA levels at either 3 or 14 days compared with the control tissue culture plastic. Furthermore, rhBMP-9 increased osteocalcin mRNA levels and alizarin red staining at 14 days compared with the control tissue culture plastic. CONCLUSION:The results from this study suggest that both porcine-derived collagen membranes combined with rhBMP-9 accelerated the osteopromotive potential of ST2 cells. Interestingly, rhBMP-9 demonstrated additional osteogenic differentiation compared with rhBMP-2 and may serve as a suitable growth factor for future clinical use. |
| 巻・号 | 32(4) |
| ページ | e221-e230 |
| 公開日 | 2017-1-1 |
| DOI | 10.11607/jomi.5652 |
| PMID | 28708926 |
| MeSH | Alkaline Phosphatase / genetics Alkaline Phosphatase / metabolism Animals Bone Morphogenetic Protein 2 / pharmacology* Cell Differentiation Cell Proliferation Collagen / metabolism* Core Binding Factor Alpha 1 Subunit / metabolism Enzyme-Linked Immunosorbent Assay Growth Differentiation Factor 2 / pharmacology* Humans Mice Osteoblasts / drug effects* Osteoblasts / metabolism Osteocalcin / metabolism Osteogenesis RNA, Messenger / genetics Real-Time Polymerase Chain Reaction Recombinant Proteins / pharmacology Stromal Cells Swine Transforming Growth Factor beta / pharmacology* |
| IF | 2.32 |
| リソース情報 | |
| ヒト・動物細胞 | ST2(RCB0224) |