PMID- 24278942 OWN - NLM STAT- MEDLINE DCOM- 20140430 LR - 20181202 IS - 1942-4434 (Electronic) IS - 0882-2786 (Linking) VI - 28 IP - 6 DP - 2013 Nov-Dec TI - In vitro and in vivo osteoinductive and osteoconductive properties of a synthetic bone substitute. PG - e432-9 LID - 10.11607/jomi.te23 [doi] AB - PURPOSE: The present study tested a recently introduced bone substitute material (BSM) with a novel structure to determine its osteoinductive and osteoconductive properties in vitro and in vivo. The specific aims were to determine the microstructure of the as-manufactured BSM, as analyzed with scanning electron microscopy, and to characterize different cellular interactions. MATERIALS AND METHODS: Human bone marrow stromal cells were cultured in the presence of the BSM. In vitro, attachment of osteoblastlike cells (SAOS-2) to the BSM was observed with the scanning electron microscope. The expression of genes related to osteogenic differentiation (alkaline phosphatase, bone sialoprotein, type I collagen, and osteocalcin) was determined by reverse-transcriptase polymerase chain reaction. In vivo, bone formation was examined with a murine model of ectopic bone formation through histology and computed tomographic scanning by using tissue-engineered constructs with the BSM and ovine bone marrow stromal cells. RESULTS: Early cellular attachment could be detected as early as 6 hours. Cellular morphology developed in the following 66 hours toward a starlike appearance. Human bone marrow stromal cells cultured in the presence of the BSM showed no reduction in their viability. Osteocalcin was up-regulated during cell culturing, demonstrating an osteoinductive effect of BSM. Histologic and computed tomographic analyses showed the formation of new bone surrounding BSM particles, and a vascular meshwork was observed in the porosity of the particles. CONCLUSION: The analyzed bone substitute of synthetic origin presented osteoinductive properties that may exert a differentiative stimulus upon osteoprogenitor cells. The tested material allowed cellular adhesion of osteoblastlike cells and, following tissue construct implantation in vivo, supported the formation of new bone. FAU - Conserva, Enrico AU - Conserva E FAU - Foschi, Federico AU - Foschi F FAU - Cancedda, Ranieri AU - Cancedda R FAU - Mastrogiacomo, Maddalena AU - Mastrogiacomo M LA - eng PT - Journal Article PL - United States TA - Int J Oral Maxillofac Implants JT - The International journal of oral & maxillofacial implants JID - 8611905 RN - 0 (Bone Substitutes) RN - 0 (Collagen Type I) RN - 0 (Integrin-Binding Sialoprotein) RN - 104982-03-8 (Osteocalcin) RN - EC 3.1.3.1 (Alkaline Phosphatase) SB - IM MH - Alkaline Phosphatase/genetics/metabolism MH - Animals MH - Bone Marrow Cells/*physiology MH - Bone Regeneration/*physiology MH - *Bone Substitutes MH - Bone and Bones/metabolism MH - Cell Adhesion/physiology MH - Cell Differentiation MH - Collagen Type I/genetics/metabolism MH - Gene Expression MH - Humans MH - Integrin-Binding Sialoprotein/genetics/metabolism MH - Mice MH - Microscopy, Electron, Scanning MH - Osteoblasts/physiology MH - Osteocalcin/genetics/metabolism MH - Porosity MH - Reverse Transcriptase Polymerase Chain Reaction MH - Sheep MH - Stromal Cells/*physiology MH - Time Factors MH - Tissue Engineering/methods EDAT- 2013/11/28 06:00 MHDA- 2014/05/03 06:00 CRDT- 2013/11/27 06:00 PHST- 2013/11/27 06:00 [entrez] PHST- 2013/11/28 06:00 [pubmed] PHST- 2014/05/03 06:00 [medline] AID - 10.11607/jomi.te23 [doi] PST - ppublish SO - Int J Oral Maxillofac Implants. 2013 Nov-Dec;28(6):e432-9. doi: 10.11607/jomi.te23.