J Appl Biomed 17:125-135, 2019 | DOI: 10.32725/jab.2019.004
Cross talk between redox signalling and metabolic activity of osteoblasts and fibroblasts in the presence of hydroxyapatite-based biomaterials influences bone regeneration
- 1 Medical University of Bialystok, Faculty of Pharmacy, Department of Analytical Chemistry, Bialystok, Poland
- 2 Medical University of Bialystok, Faculty of Medicine, Department of Integratet Dentistry, Bialystok, Poland
- 3 Medical University of Bialystok, Faculty of Pharmacy, Department of Medicinal Chemistry, Bialystok, Poland
Regeneration of bone tissue defects that result from metabolic disorders, including periodontal diseases, can be supported by biomaterials based on hydroxyapatite. Despite of good biocompatibility of biomaterials they can cause oxidative stress and inflammatory processes as a result of mechanical interaction with surrounding tissues. Because osteoblasts are responsible for bone regeneration process in which gingival fibroblasts may also participate, the aim of the work was to investigate the influence of hydroxyapatite-based biomaterials (allogeneic and xenogeneic) and biomaterials combined with enamel matrix derivative (Emdogain) on osteoblast and fibroblast redox balance in the context of osteoblast proliferation and differentiation. The results showed that examined substitutes were not cytotoxic in vitro, but affected redox balance of osteoblasts and fibroblasts (ROS level increase and GSH level decrease) which led to oxidative stress (MDA and protein carbonyl groups level increase) resulting in an increase of the Nrf2 and NFκB expression. The consequence of these changes was partial inhibition of proliferation and osteoblast differentiation. Emdogain alone and combined with biomaterials decreased ROS generation and increased GSH level in both osteoblasts and fibroblasts leading to reduction of transcription factors expression especially proinflammatory NFκB, which promoted osteoblast differentiation and mineralization process.
Keywords: Biomaterials; Bone regeneration; Fibroblasts; Osteoblasts; Oxidative stress
Conflicts of interest:
The authors have no conflict of interests to declare.
Received: November 6, 2018; Accepted: January 23, 2019; Prepublished online: April 15, 2019; Published: June 28, 2019 Show citation
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