Osteogenic Activity of the Fourteen Types of Human Bone Morphogenetic Proteins (BMPs)

• Published in: Journal of bone and joint surgery. American volume Vol. 85; no. 8; pp. 1544 - 1552
• Main Authors: Cheng, Hongwei, Jiang, Wei, Phillips, Frank M, Haydon, Rex C, Peng, Ying, Zhou, Lan, Luu, Hue H, An, Naili, Breyer, Benjamin, Vanichakarn, Pantila, Szatkowski, Jan Paul, Park, Jae Yoon, He, Tong-Chuan
• Format: Journal Article
• Language: English
• Published: United States Copyright by The Journal of Bone and Joint Surgery, Incorporated 01.08.2003; Journal of Bone and Joint Surgery AMERICAN VOLUME
• Edition: American volume
• Subjects: Adenoviridae - genetics; Alkaline Phosphatase - metabolism; Animals; Bone Density - physiology; Bone Morphogenetic Proteins - classification; Bone Morphogenetic Proteins - genetics; Bone Morphogenetic Proteins - pharmacology; Cell Line; Gene Transfer Techniques; Humans; Mesoderm - cytology; Mice; Osteoblasts - drug effects; Osteocytes - drug effects; Osteogenesis - drug effects; Osteosarcoma; Stem Cells - drug effects; Tumor Cells, Cultured
• DOI: 10.2106/00004623-200308000-00017
• ISSN: 0021-9355

BackgroundBone morphogenic proteins (BMPs) are known to promote osteogenesis, and clinical trials are currently underway to evaluate the ability of certain BMPs to promote fracture-healing and spinal fusion. The optimal BMPs to be used in different clinical applications have not been elucidated, and a comprehensive evaluation of the relative osteogenic activity of different BMPs is lacking.MethodsTo identify the BMPs that may possess the most osteoinductive activity, we analyzed the osteogenic activity of BMPs in mesenchymal progenitor and osteoblastic cells. Recombinant adenoviruses expressing fourteen human BMPs (BMP-2 to BMP-15) were constructed to infect pluripotent mesenchymal progenitor C3H10T1/2 cells, preosteoblastic C2C12 cells, and osteoblastic TE-85 cells. Osteogenic activity was determined by measuring the induction of alkaline phosphatase, osteocalcin, and matrix mineralization upon BMP stimulation.ResultsBMP-2, 6, and 9 significantly induced alkaline phosphatase activity in pluripotential C3H10T1/2 cells, while BMP-2, 4, 6, 7, and 9 significantly induced alkaline phosphatase activity in preosteoblastic C2C12 cells. In TE-85 osteoblastic cells, most BMPs (except BMP-3 and 12) were able to induce alkaline phosphatase activity. The results of alkaline phosphatase histochemical staining assays were consistent with those of alkaline phosphatase colorimetric assays. Furthermore, BMP-2, 6, and 9 (as well as BMP-4 and, to a lesser extent, BMP-7) significantly induced osteocalcin expression in C3H10T1/2 cells. In C2C12 cells, osteocalcin expression was strongly induced by BMP-2, 4, 6, 7, and 9. Mineralized nodules were readily detected in C3H10T1/2 cells infected with BMP-2, 6, and 9 (and, to a lesser extent, those infected with BMP-4 and 7).ConclusionsA comprehensive analysis of the osteogenic activity of fourteen types of BMPs in osteoblastic progenitor cells was conducted. Our results suggest an osteogenic hierarchical model in which BMP-2, 6, and 9 may play an important role in inducing osteoblast differentiation of mesenchymal stem cells. In contrast, most BMPs are able to stimulate osteogenesis in mature osteoblasts.Clinical RelevanceThese findings have implications for the development of effective formulas for bone-healing and spinal fusion. The efficacy of osteogenesis may depend not only on the type of BMP or the combination of BMPs that is used but also on the cell types that are present.