TY - JOUR
T1 - Biological role of synthetic octacalcium phosphate in bone formation and mineralization
AU - Suzuki, Osamu
N1 - Funding Information:
A series of studies using synthetic OCP was supported in part by Grants-in-Aid (17076001, 19390490, and 20659304)from the Ministry of Education, Culture, Sports, Science and Technology of Japan and by the Uehara Memorial Foundation. The author thanks Masatoshi Yamada, JGC Corporation, for assistance in the TEM study. The author also thanks Dr. Hideki Imaizumi, Osaki Citizen Hospital, Professor Takenobu Katagiri, Saitama Medical University Research Center for Genomic Medicine, Professors Ryutaro Kamijo, Masanori Nakamura, and Dr. Masamichi Takami, Showa University School of Dentistry, Professors Shinji Kamakura and Eiji Itoi, and Emeritus Professors Minoru Sakurai and Manabu Kagayama, Tohoku University Graduate School, Professor Takaaki Aoba, Nippon Dental University, and Drs. Takahisa Anada and Yoshitomo Honda of Divi- sion of Craniofacial Function Engineering, Tohoku University Graduate School of Dentistry.
PY - 2010
Y1 - 2010
N2 - Bone formation, including matrix mineralization by calcium phosphate crystals, is essentially organized under the control of osteoblasts. Great efforts have been conducted to establish the linkage between bio-crystals and synthetic crystals to determine the physicochemical properties of these crystals. Octacalcium phosphate-OCP-has been proposed to be a precursor of hydroxyapatite-HA-, the prototype in bone and tooth apatite crystals, and suggested to have a role in apatite crystal development. Studies using synthetic OCP provided evidence that this mineral phase stimulates bone formation more than synthetic HA if implanted in bone defects during conversion from OCP to HA. Furthermore, the enhancement of bone formation was usually accompanied by osteoclastic resorption of OCP. In vitro studies showed that OCP is capable of stimulating mouse bone marrow stromal cells to differentiate into osteoblastic cells and osteoclast formation in co-culture by enhancing the expression of the receptor activator of NF-κB ligand -RANKL-in osteoblastic cells. Although the precise mechanism of the precursor precipitation and subsequent apatite formation has not been fully elucidated in normal bone mineralization, it is likely that the OCP precursor plays a role in the stimulation of bone-forming cells through interaction with the surrounding tissue environment if this mineral phase is involved in bone formation.
AB - Bone formation, including matrix mineralization by calcium phosphate crystals, is essentially organized under the control of osteoblasts. Great efforts have been conducted to establish the linkage between bio-crystals and synthetic crystals to determine the physicochemical properties of these crystals. Octacalcium phosphate-OCP-has been proposed to be a precursor of hydroxyapatite-HA-, the prototype in bone and tooth apatite crystals, and suggested to have a role in apatite crystal development. Studies using synthetic OCP provided evidence that this mineral phase stimulates bone formation more than synthetic HA if implanted in bone defects during conversion from OCP to HA. Furthermore, the enhancement of bone formation was usually accompanied by osteoclastic resorption of OCP. In vitro studies showed that OCP is capable of stimulating mouse bone marrow stromal cells to differentiate into osteoblastic cells and osteoclast formation in co-culture by enhancing the expression of the receptor activator of NF-κB ligand -RANKL-in osteoblastic cells. Although the precise mechanism of the precursor precipitation and subsequent apatite formation has not been fully elucidated in normal bone mineralization, it is likely that the OCP precursor plays a role in the stimulation of bone-forming cells through interaction with the surrounding tissue environment if this mineral phase is involved in bone formation.
KW - Bone
KW - Hydroxyapatite
KW - Mineralization
KW - Octacalcium phosphate
KW - Precursor
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U2 - 10.2330/joralbiosci.52.6
DO - 10.2330/joralbiosci.52.6
M3 - Review article
AN - SCOPUS:79952220559
SN - 1349-0079
VL - 52
SP - 6
EP - 14
JO - Journal of Oral Biosciences
JF - Journal of Oral Biosciences
IS - 1
ER -