Human amniotic membrane extracellular matrix scaffold for dental pulp regeneration in vitro and in vivo

• DOI: 10.1111/iej.13675
• Publication Date: 2021-12-19T06:24:49Z
• Authors: Hengameh Bakhtiar; Azin Ashoori; Sarah Rajabi; Mohamad Pezeshki‐...; Alireza Ayati; Mohammad Reza Mou...; Mohammad Reza Ellini; Amir Kamali; Amir Azarpazhooh; Anil Kishen
• Keywords: 0301 basic medicine; 03 medical and health sciences; Tissue Engineering; Tissue Scaffolds; Humans; Regeneration; Cell Differentiation; Amnion; Dental Pulp; Extracellular Matrix

AbstractAimIn order to obtain a 3‐dimentional scaffold with predictable clinical results for pulp regeneration, this study aims to fabricate and characterize a porous decellularized human amniotic membrane (HAM) extracellular matrix (ECM) scaffold, and evaluate its potential to promote pulp regeneration in vitro and in vivo.MethodologyThe HAM was decellularized, and its histology and DNA content were analysed to confirm decellularization. The scaffolds were synthesized with 15, 22.5 and 30 mg/ml concentrations. The porosity, pore size, phosphate‐buffered saline (PBS) absorption and degradation rate of the scaffolds were assessed. In vitro experiments were performed on human dental pulp stem cells (hDPSCs) to assess their viability, proliferation, adhesion and migration on the scaffolds. The optimal group was selected for in vivo immunogenicity assessment and was also used as the cell‐free or cell‐loaded scaffold in root segment models to evaluate pulp regeneration. All nonparametric data were analysed with the Kruskal–Wallis test followed by Dunn's post hoc test, whilst quantitative data were analysed with one‐way anova.ResultsDecellularization of HAM was confirmed (p < .05). The porosity of all scaffolds was more than 95%, and the pore size decreased with an increase in ECM concentration (p < .01). PBS absorption was not significantly different amongst the groups, whilst 30 mg/ml ECM scaffold had the highest degradation rate (p < .01). The hDPSCs adhered to the scaffold, whilst their proliferation rate increased over time in all groups (p < .001). Cell migration was higher in 30 mg/ml ECM scaffold (p < .05). In vivo investigation with 30 mg/ml ECM scaffold revealed mild to moderate inflammatory response. In root segments, both cell‐free and cell‐loaded 30 mg/ml scaffolds were replaced with newly formed, pulp‐like tissue with no significant difference between groups. Immunohistochemical assessments revealed high revascularization and collagen content with no significant difference amongst the groups.ConclusionThe 30 mg/ml HAM ECM scaffold had optimal physical properties and better supported hDPSC migration. The HAM ECM scaffold did not interfere with formation of pulp‐like tissue and revascularization within the root canal when employed as both cell‐free and cell‐loaded scaffold. These results highlight the potential of HAM ECM membrane for further investigations in regenerative endodontics.