BONE MORPHOGENETIC PROTEIN-2 AND COLLAGEN TYPE 1 FROM DIFFERENT SOURCES OF DEMINERALIZED DENTINE MATRIX: RELEASE KINETIC AND CHEMOTAXIS POTENTIAL FOR OSTEOPROGENITOR CELLS

Authors

  • JIBO BAO Department of Oral Biology, Faculty of Dentistry, Mahidol University, Rajthevi, Bangkok, Thailand.
  • JUN H. E. Qianxing Road Dental Clinic, The Affiliated Stomatology Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
  • ZILIANG L. I. Qianxing Road Dental Clinic, The Affiliated Stomatology Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
  • RONGQIANG YANG The Affiliated Stomatology Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
  • JINYANG ZOU Department of Prosthodontics, School of Stomatology, Kunming Medical University, Kunming, Yunnan Province, China.
  • YIXIN DING Department of Prosthodontics, School of Stomatology, Kunming Medical University, Kunming, Yunnan Province, China.
  • TAO NIU Department of Prosthodontics, School of Stomatology, Kunming Medical University, Kunming, Yunnan Province, China.
  • ZHIGANG XIE Department of Implantology and Prosthodontics, The Affiliated Stomatology Hospital of Kunming Medical University, Kunming, Yunnan Province, China.
  • DUTMANEE SERIWATANACHAI Department of Oral Biology, Faculty of Dentistry, Mahidol University, Rajthevi, Bangkok, Thailand.

DOI:

https://doi.org/10.22159/ijap.2019.v11s1.18475

Keywords:

Demineralized dentine matrix, Chemotaxis, Cell migration, Osteoinduction, bone grafting

Abstract

Objective: To investigate the release of bone morphogenetic protein-2 (BMP-2) and collagen type I proteins (COL1) from different sources of
demineralized dentine matrix (DDM) and their chemotaxis to mouse osteoprogenitor cells.
Methods: The release kinetic of BMP-2 and COL1 was measured from custom-made DDM (CMDDM) and commercially available DDM (CADDM).
Using Urist physicochemical method, CMDDM was collected from the extracted teeth in a certified dental clinic. Levels of BMP-2 and COL1 released
were measured at days 1, 2, 3, 5, 7, 9, 11, and 13. Next, mouse osteoprogenitor cells, MC3T3-E1, were cultured with a variety of materials as follows:
CMDDM, CADDM, Bio-Oss®, and blank control in transwell system. The number of cell migration was determined by crystal violet staining to explore
chemotaxis of different DDMs to mouse osteoprogenitor cells.
Results: BMP-2 was detected at 588.32 ± 14.53 pg/ml from 5 g of CMDDM. In the release kinetic assay, the concentration of BMP-2 in the CMDDM
group increased rapidly and peaked at 113.9 pg/ml on day 5, almost four times higher than that of CADDM. The release of COL1 showed similar
pattern in both CMDDM and CADDM; however, the amount was significantly higher in the CMDDM group. In cell culture experiment, the number of
migrated MC3T3-E1 was ranked as the highest in CMDDM, followed by CADDM and Bio-Oss® (p<0.05).
Conclusion: CMDDM released BMP-2 and COL1 greater than CADDM, which can induce more osteoblast-like cell migration. These results demonstrated
a release kinetic of proteins and osteoinductivity of CMDDM, which supports a benefit of using autogenous bone graft.

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Published

05-04-2019

How to Cite

BAO, J., H. E., J., L. I., Z., YANG, R., ZOU, J., DING, Y., NIU, T., XIE, Z. ., & SERIWATANACHAI, D. (2019). BONE MORPHOGENETIC PROTEIN-2 AND COLLAGEN TYPE 1 FROM DIFFERENT SOURCES OF DEMINERALIZED DENTINE MATRIX: RELEASE KINETIC AND CHEMOTAXIS POTENTIAL FOR OSTEOPROGENITOR CELLS. International Journal of Applied Pharmaceutics, 11(1), 223–229. https://doi.org/10.22159/ijap.2019.v11s1.18475

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