Combined effects of melatonin and FGF-2 on mouse preosteoblast behavior within interconnected porous hydroxyapatite ceramics - in vitro analysis

Authors

  • Mohammad Zeshaan RAHMAN Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Surgery
  • Hideo SHIGEISHI Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Surgery
  • Kazuki SASAKI Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Surgery
  • Akira OTA Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Surgery
  • Kouji OHTA Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Surgery
  • Masaaki TAKECHI Hiroshima University; Institute of Biomedical and Health Sciences; Department of Oral and Maxillofacial Surgery

DOI:

https://doi.org/10.1590/1678-775720150606

Abstract

Objective Biocompatible materials such as interconnected porous hydroxyapatite ceramics (IP-CHA) loaded with osteogenic cells and bioactive agents are part of an evolving concept for overcoming craniofacial defects by use of artificial bone tissue regeneration. Amongst the bioactive agents, melatonin (MEL) and basic fibroblast growth factor (FGF-2) have been independently reported to induce osteoblastic activity. The present in vitro study was undertaken to examine the relationship between these two bioactive agents and their combinatory effects on osteoblastic activity and mineralization in vitro. Material and Methods Mouse preosteoblast cells (MC3T3-E1) were seeded and cultured within cylindrical type of IP-CHA block (ø 4x7 mm) by vacuum-assisted method. The IP-CHA/MC3T3 composites were subjected to FGF-2 and/or MEL. The proliferation assay, alkaline phosphatase enzyme activity (ALP), mRNA expressions of late bone markers, namely Osteocalcin (OCN) and Osteopontin (OPN), and Alizarin Red staining were examined over a period of 7 days. Results FGF-2 mainly enhanced the proliferation of MC3T3-E1 cells within the IP-CHA constructs. MEL mainly induced the mRNA expression of late bone markers (OCN and OPN) and showed increased ALP activity of MC3T3 cells cultured within IP-CHA construct. Moreover, the combination of FGF-2 and MEL showed increased osteogenic activity within the IP-CHA construct in terms of cell proliferation, upregulated expressions of OCN and OPN, increased ALP activity and mineralization with Alizarin Red. The synergy of the proliferative potential of FGF-2 and the differentiation potential of MEL showed increased osteogenic activity in MC3T3-E1 cells cultured within IP-CHA constructs. Conclusion These findings indicate that the combination of FGF-2 and MEL may be utilized with biocompatible materials to attain augmented osteogenic activity and mineralization.

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Published

2016-04-01

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Section

Original Articles