Non-surgical model for alveolar bone regeneration by bone morphogenetic protein-2/7 gene therapy

• Published in: Journal of periodontology (1970) Vol. 89; no. 1; p. 85
• Main Authors: Kawai, Mariko, Kataoka, Yo-Hei, Sonobe, Junya, Yamamoto, Hiromitsu, Inubushi, Masakazu, Ishimoto, Takuya, Nakano, Takayoshi, Maruyama, Hiroki, Miyazaki, Jun-Ichi, Yamamoto, Toshio, Bessho, Kazuhisa, Ohura, Kiyoshi
• Format: Journal Article
• Language: English
• Published: United States 01.01.2018
• Subjects: electroporation; plasmids; periodontium; regeneration; bone and bones; bone morphogenetic proteins
• ISSN: 1943-3670
• DOI: 10.1902/jop.2017.170328

Alveolar bone is a critical tissue for tooth retention; however, once alveolar bone is lost, it may not spontaneously regenerate. Currently, bone grafts or artificial bone is commonly used for alveolar bone regeneration therapy. However, these therapies require surgical procedures, which present risks, particularly in elderly patients. Therefore, development of alveolar bone regeneration techniques that do not require surgical procedures is critical. It is well known that stem cells present in the periosteal and periodontal ligament may be induced to differentiate into osteogenic cells. This study hypothesizes that transfer of the bone morphogenetic protein-2/7 (BMP-2/7) gene into periodontal tissues via in vivo electroporation induces exogenous BMP production and causes stem cells in periodontal tissues to differentiate into osteogenic cells, enabling generation of new alveolar bone. The BMP-2/7 gene expression vector was introduced via electroporation into the target site in periodontal tissues of the first molar of rat maxillae. Exogenous BMP-2 and -7 were detected in the target areas, and growth of new alveolar bone tissue was observed 5 days after gene transfer. On day 7, new alveolar bone tissues were found to connect to the original bone tissues. Moreover, mineral apposition rates of the alveolar bone after BMP-2/7 gene transfer were significantly higher than those in the control group after LacZ gene transfer. The present findings indicate that a combination of the BMP-2/7 non-viral vector and in vivo electroporation represents a promising non-surgical option for alveolar bone regeneration therapy.