Harnessing the Regenerative Potential of Purified Bovine Dental Pulp and Dentin Extracellular Matrices in a Chitosan/Alginate Hydrogel

Author:

Gould Maree L.1ORCID,Downes Nerida J.1,Woolley Adele G.2ORCID,Hussaini Haizal M.13ORCID,Ratnayake Jithendra T.1ORCID,Ali Mohammad Azam1ORCID,Friedlander Lara T.1ORCID,Cooper Paul R.1ORCID

Affiliation:

1. Faculty of Dentistry Sir John Walsh Research Institute University of Otago P.O. Box 56 Dunedin 9054 New Zealand

2. Maurice Wilkins Centre for Biodiscovery University of Otago P.O. Box 56 Dunedin 9054 New Zealand

3. Faculty of Dental Medicine University of Airlangga Surabaya 60132 Indonesia

Abstract

AbstractWhen a tooth is diseased or damaged through caries, bioactive molecules are liberated from the pulp and dentin as part of the natural response to injury and these are key molecules for stimulating stem cell responses for tissue repair. Incorporation of these extracellular‐matrix (ECM)‐derived molecules into a hydrogel model can mimic in vivo conditions to enable dentin–pulp complex regeneration. Here, a chitosan/alginate (C/A) hydrogel is developed to sequester bovine ECM extracts. Human dental pulp cells (hDPCs) are cultured with these constructs and proliferation and cytotoxicity assays confirm that these C/A hydrogels are bioactive. Sequential z‐axis fluorescent imaging visualizes hDPCs protruding into the hydrogel as it degraded. Alizarin red S staining shows that hDPCs cultured with the hydrogels display increased calcium‐ion deposition, with dentin ECM stimulating the highest levels. Alkaline phosphatase activity is increased, as is expression of transforming growth factor‐beta as demonstrated using immunocytochemistry. Directional analysis following phase contrast kinetic image capture demonstrates that both dentin and pulp ECM molecules act as chemoattractants for hDPCs. Data from this study demonstrate that purified ECM from dental pulp and dentin when delivered in a C/A hydrogel stimulates dental tissue repair processes in vitro.

Publisher

Wiley

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