Ex-vivo recellularisation and stem cell differentiation of a decellularised rat dental pulp matrix

• Published in: Scientific reports 2020-12, Vol.10 (1), p.21553-21553, Article 21553
• Main Authors: Matoug-Elwerfelli, Manal, Nazzal, Hani, Raif, El Mostafa, Wilshaw, Stacy-Paul, Esteves, Filomena, Duggal, Monty
• Format: Article
• Language: English
• Subjects: 631/1647; 631/532; 639/301; 692/700; Animals; Biocompatibility; Cell culture; Cell differentiation; Cell Differentiation - physiology; Cell survival; Cell viability; Cytoskeleton; Cytotoxicity; Dental pulp; Dental Pulp - cytology; Feasibility studies; Growth factors; Humanities and Social Sciences; Immunohistochemistry; multidisciplinary; Rats; Repopulation; Scanning electron microscopy; Science; Science (multidisciplinary); Stem cell transplantation; Stem cells; Stem Cells - cytology; Teeth; Tissue Engineering; Tissue Scaffolds
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-78477-x

Implementing the principles of tissue engineering within the clinical management of non-vital immature permanent teeth is of clinical interest. However, the ideal scaffold remains elusive. The aim of this work was to assess the feasibility of decellularising rat dental pulp tissue and evaluate the ability of such scaffold to support stem cell repopulation. Rat dental pulps were retrieved and divided into control and decellularised groups. The decellularisation protocol incorporated a low detergent concentration and hypotonic buffers. After decellularisation, the scaffolds were characterised histologically, immunohistochemistry and the residual DNA content quantified. Surface topography was also viewed under scanning electron microscopy. Biocompatibility was evaluated using cytotoxicity assays utilising L-929 cell line. Decellularised scaffolds were recellularised with human dental pulp stem cells up to 14 days in vitro. Cellular viability was assessed using LIVE/DEAD stain kit and the recellularised scaffolds were further assessed histologically and immunolabelled using makers for odontoblastic differentiation, cytoskeleton components and growth factors. Analysis of the decellularised scaffolds revealed an acellular matrix with histological preservation of structural components. Decellularised scaffolds were biocompatible and able to support stem cell survival following recellularisation. Immunolabelling of the recellularised scaffolds demonstrated positive cellular expression against the tested markers in culture. This study has demonstrated the feasibility of developing a biocompatible decellularised dental pulp scaffold, which is able to support dental pulp stem cell repopulation. Clinically, decellularised pulp tissue could possibly be a suitable scaffold for use within regenerative (reparative) endodontic techniques.