TY - JOUR
T1 - Octacalcium phosphate collagen composite stimulates the expression and activity of osteogenic factors to promote bone regeneration
AU - Kouketsu, Atsumu
AU - Matsui, Keiko
AU - Kawai, Tadashi
AU - Ezoe, Yushi
AU - Yanagisawa, Toshiki
AU - Yasuda, Ayato
AU - Takahashi, Tetsu
AU - Kamakura, Shinji
N1 - Funding Information:
This study was supported in part by grants-in-aid (nos. 16H03159, 16K11741, and 18K19891) from the Ministry of Education, Science, Sports and Culture of Japan. One of the authors (SK) has obtained a patent onOCP/Col in Japan (#5046511).
Funding Information:
This study was supported in part by grants‐in‐aid (nos. 16H03159, 16K11741, and 18K19891) from the Ministry of Education, Science, Sports and Culture of Japan. One of the authors (SK) has obtained a patent onOCP/Col in Japan (#5046511).
Publisher Copyright:
© 2019 The Authors. Journal of Tissue Engineering and Regenerative Medicine published by John Wiley & Sons Ltd
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Objective: This study investigated the bone regenerative properties of an octacalcium phosphate collagen composite (OCP/Col) in a rat calvarial bone defect model. Design: An OCP/Col or β-tricalcium phosphate (β-TCP)/Col disk was implanted into the critical-sized calvarial defects and fixed 2 or 4 weeks later. The radiopacity of defects was examined after disk implantation by the radiographic examination and micro-computed tomography (μ-CT). Immunohistochemical and histochemical analyses were carried out to assess the bone matrix maturation, neovascularization, and osteoclast and osteoblast distribution in the neonatal bone. Results: Radiographic and μ-CT examination of the area of implanted OCP/Col indicated the newly formed bone and no difference from those of the original bone. Osteopontin, osteocalcin, Runt-related transcription factor 2, type 1 collagen, vascular endothelial growth factor, and alkaline phosphatase or tartrate-resistant acid phosphatase in the newly formed calvarial bone and the surrounding connective tissue were detected by immunohistochemistry and histochemistry. Biomarker expression was not significantly elevated at the defect site; the area of which was calculated by dividing the distance from the healthy bone margin or calvarium and dura mater surface. There was no difference in the expression of these biomarkers in the OCP/Col group at 2 and 4 weeks after surgery. In addition, the expression levels of all markers were higher in the OCP/Col group than in the β-TCP/Col group at 2 and 4 weeks after surgery. Conclusions: The OCP/Col as a bone regeneration material not only exhibits osteoconductive activity that is dependent on residual healthy bone tissue, but also has osteoinductive capacity, which promotes angiogenesis and osteogenic cell invasion from host tissue into the bone defect.
AB - Objective: This study investigated the bone regenerative properties of an octacalcium phosphate collagen composite (OCP/Col) in a rat calvarial bone defect model. Design: An OCP/Col or β-tricalcium phosphate (β-TCP)/Col disk was implanted into the critical-sized calvarial defects and fixed 2 or 4 weeks later. The radiopacity of defects was examined after disk implantation by the radiographic examination and micro-computed tomography (μ-CT). Immunohistochemical and histochemical analyses were carried out to assess the bone matrix maturation, neovascularization, and osteoclast and osteoblast distribution in the neonatal bone. Results: Radiographic and μ-CT examination of the area of implanted OCP/Col indicated the newly formed bone and no difference from those of the original bone. Osteopontin, osteocalcin, Runt-related transcription factor 2, type 1 collagen, vascular endothelial growth factor, and alkaline phosphatase or tartrate-resistant acid phosphatase in the newly formed calvarial bone and the surrounding connective tissue were detected by immunohistochemistry and histochemistry. Biomarker expression was not significantly elevated at the defect site; the area of which was calculated by dividing the distance from the healthy bone margin or calvarium and dura mater surface. There was no difference in the expression of these biomarkers in the OCP/Col group at 2 and 4 weeks after surgery. In addition, the expression levels of all markers were higher in the OCP/Col group than in the β-TCP/Col group at 2 and 4 weeks after surgery. Conclusions: The OCP/Col as a bone regeneration material not only exhibits osteoconductive activity that is dependent on residual healthy bone tissue, but also has osteoinductive capacity, which promotes angiogenesis and osteogenic cell invasion from host tissue into the bone defect.
KW - bone regeneration
KW - bone tissue engineering
KW - octacalcium phosphate collagen composite
KW - osteogenic factors
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U2 - 10.1002/term.2969
DO - 10.1002/term.2969
M3 - Article
C2 - 31721475
AN - SCOPUS:85075013285
SN - 1932-6254
VL - 14
SP - 99
EP - 107
JO - Journal of Tissue Engineering and Regenerative Medicine
JF - Journal of Tissue Engineering and Regenerative Medicine
IS - 1
ER -