Clinical Potential of Long‐Term Cryopreserved Stem Cells From Impacted Third Molar Pulps for Regenerative Endodontic Procedures: An Ex Vivo Evaluation

This study aimed to establish a standardised protocol for isolating dental pulp stem cells (DPSCs) from fully impacted third molar teeth and to assess the effect of long-term cryopreservation on their viability for future clinical applications in regenerative endodontics. DPSCs were isolated from 21 impacted third molars. The clinical relevance of these cells was characterised via flow cytometry, confirming that 96% expressed mesenchymal stem cell markers. Seventeen samples were cryopreserved at -86°C for up to 12 months to evaluate biological stability for autologous transplantation. The standardised surgical extraction and isolation protocol yielded a high concentration of therapeutic-grade cells (3.43 × 10<sup>6</sup> cells/mL). Post-thaw viability remained stable (74% to 99%) over 12 months. Importantly, the cells maintained consistent morphology, suggesting they retained the biological potential necessary for dentine-pulp complex regeneration. The results validate a reliable long-term DPSC preservation protocol, supporting feasible dental stem cell banking and a source of viable cells for regenerative endodontic procedures.

Authors

Institutions

Publication Details

Journal
Australian Endodontic Journal
Published
2026-03-13
DOI
https://doi.org/10.1111/aej.70071
Primary Topic
Mesenchymal stem cell research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Clinical Potential of Long‐Term Cryopreserved Stem Cells From Impacted Third Molar Pulps for Regenerative Endodontic Procedures: An Ex Vivo Evaluation

Yiğit Uyanıkgil, Gözde Kandemir Demirci, Birant Şimşek, Mehmet Emin Kaval et al.
Australian Endodontic Journal
Mesenchymal stem cell research
article

Clinical Potential of Long‐Term Cryopreserved Stem Cells From Impacted Third Molar Pulps for Regenerative Endodontic Procedures: An Ex Vivo Evaluation

Yiğit Uyanıkgil, Gözde Kandemir Demirci, Birant Şimşek, Mehmet Emin Kaval, Özgün Selim Germiyan, Timur Köse, Pelin Güneri, Uğur Tekin
article en

Abstract

This study aimed to establish a standardised protocol for isolating dental pulp stem cells (DPSCs) from fully impacted third molar teeth and to assess the effect of long-term cryopreservation on their viability for future clinical applications in regenerative endodontics. DPSCs were isolated from 21 impacted third molars. The clinical relevance of these cells was characterised via flow cytometry, confirming that 96% expressed mesenchymal stem cell markers. Seventeen samples were cryopreserved at -86°C for up to 12 months to evaluate biological stability for autologous transplantation. The standardised surgical extraction and isolation protocol yielded a high concentration of therapeutic-grade cells (3.43 × 10<sup>6</sup> cells/mL). Post-thaw viability remained stable (74% to 99%) over 12 months. Importantly, the cells maintained consistent morphology, suggesting they retained the biological potential necessary for dentine-pulp complex regeneration. The results validate a reliable long-term DPSC preservation protocol, supporting feasible dental stem cell banking and a source of viable cells for regenerative endodontic procedures.

Australian Endodontic Journal
Ege University (TR)
Openalex Percentile: Top 24%
Mesenchymal stem cell research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.