TY - JOUR
T1 - Degradation of extracellular matrices propagates calcification during development and healing in bones and teeth
AU - Sasano, Yasuyuki
AU - Nakamura, Megumi
AU - Henmi, Akiko
AU - Okata, Hiroshi
AU - Suzuki, Osamu
AU - Kayaba, Atsuko
AU - Mayanagi, Miyuki
N1 - Funding Information:
We thank Mr. Yasuto Mikami for his helpful technical assistance. This work was supported by JSPS (Japan Society for the Promotion of Science) KAKENHI Grants (Grants-in-Aid for Scientific Research); Grant Numbers: JP23592694 , JP24792170 , JP15K11002 , JP15K11003 , JP17K17081 , JP18K09517 , and JP18K09760 .
Publisher Copyright:
© 2019 Japanese Association for Oral Biology
PY - 2019/9
Y1 - 2019/9
N2 - Background: Bone, dentin, and enamel are tissues formed through calcification, a process involving deposition of calcium phosphate minerals on extracellular organic matrices. Calcification, the underlying mechanism of which is unknown, is initiated with mineral deposition followed by advancing of the deposit and subsequent maturation of the mineral crystal. Highlight: We have reviewed the current knowledge of how calcification proceeds during bone development, bone healing, and enamel and dentin development, based on reported studies. Previous studies reported by us and by other authors have suggested that degradation of some extracellular matrix (ECM) proteins is involved in calcification during bone and dentin development and bone healing in a manner similar to that previously reported for enamel development. Conclusion: The ECM proteins may inhibit mineral deposition and calcification, similar to the role of amelogenin during enamel development. The candidates for the amelogenin equivalents in bone and dentin have not been identified. Further studies are required to elucidate the regulatory mechanisms of bone and dentin calcification in light of specific ECM proteins that prevent calcification and enzymes that degrade these ECM proteins.
AB - Background: Bone, dentin, and enamel are tissues formed through calcification, a process involving deposition of calcium phosphate minerals on extracellular organic matrices. Calcification, the underlying mechanism of which is unknown, is initiated with mineral deposition followed by advancing of the deposit and subsequent maturation of the mineral crystal. Highlight: We have reviewed the current knowledge of how calcification proceeds during bone development, bone healing, and enamel and dentin development, based on reported studies. Previous studies reported by us and by other authors have suggested that degradation of some extracellular matrix (ECM) proteins is involved in calcification during bone and dentin development and bone healing in a manner similar to that previously reported for enamel development. Conclusion: The ECM proteins may inhibit mineral deposition and calcification, similar to the role of amelogenin during enamel development. The candidates for the amelogenin equivalents in bone and dentin have not been identified. Further studies are required to elucidate the regulatory mechanisms of bone and dentin calcification in light of specific ECM proteins that prevent calcification and enzymes that degrade these ECM proteins.
KW - Bone
KW - Calcification
KW - Dentin
KW - Development
KW - Matrix metalloproteinase
UR - http://www.scopus.com/inward/record.url?scp=85070918644&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85070918644&partnerID=8YFLogxK
U2 - 10.1016/j.job.2019.07.004
DO - 10.1016/j.job.2019.07.004
M3 - Review article
C2 - 31400543
AN - SCOPUS:85070918644
SN - 1349-0079
VL - 61
SP - 149
EP - 156
JO - Journal of Oral Biosciences
JF - Journal of Oral Biosciences
IS - 3
ER -