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Isolation of Mesenchymal Stem Cells from Human Alveolar Periosteum and Effects of Vitamin D on Osteogenic Activity of Periosteum-derived Cells
Published on: May 4, 2018
The effects of growth factors on the production of osteopontin and osteocalcin
Joel Davis1, Michelle Tucci, Laura Franklin
1School of Graduate Studies in Health Sciences, Department of Orthopaedic Surgery and Rehabilitation, University of Mississippi Medical Center, Jackson, MS 39216, USA. jmdavis@orthopedics.umsmed.edu
Abstract:
Bone morphogenetic proteins (BMPs) are a group of structurally related proteins in the transforming growth factor-beta (TGF-beta) family which have been shown to stimulate bone formation in vivo. Since these proteins are concentrated in the organic matrix of bone and would be released after a fracture or during bone resorption, they are likely to have a profound effect on bone remodeling and may provide a link between bone resorption and bone formation. The hypothesis of this study was that osteoblast-like cells (OBs) treated with demineralized bone matrix (DBM) would have similar levels of secretion of osteopontin (OPN) and osteocalcin (OCN) to that of OBs treated with insulin-like growth factor-1 (IGF-1), while OBs treated with bone morphogenetic protein-7, also called osteogenic protein-1 (OP-1), would secrete levels of OPN and OCN less than the DBM group. Specifically, the aims of this study were to evaluate osteoblast-like cells (MG-63 cell line) for secretion of both OPN and OCN after treatment with DBM, OP-1, or IGF-1 compared to control, at 24, 48, and 72 hours. After each incubation period, ELISA kits were used to determine the levels of osteopontin and osteocalcin production. The results clearly demonstrated a rise of OCN at 48 hours and a fall at 72 hours for all samples, including control groups. However, there was no significant difference between groups (p > 0.05). With the OPN assay, results showed no significant difference between groups until 72 hours (p = 0.022), where the IGF-1 group was significantly higher than the Control and DBM groups (p = 0.003 and p = 0.021, respectively). This information is important for understanding the signaling pathways that may be initiated in the osteoblast following stimulation with growth factors.
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