Evaluating regenerative potentialdental pulp stem cells (DPSC) and Osteobiol Gen-Os® scaffold for enhanced bone repair in rat mandibular defects

  1. Hamad A Alrashid, Haifa
Supervised by:
  1. María Begoña García Cenador Director

Defence university: Universidad de Salamanca

Defense date: 30 September 2024

Committee:
  1. Leticia Blanco Antona Chair
  2. Rita Meguerdithch Khounganian Committee member
Department: Cirugía
University: Universidad de Salamanca

Type: Dissertation

GREDOS. Repositorio Institucional de la Universidad de Salamanca: lock_openOpen access Externo

Sustainable development goals

Abstract

The therapeutic approach to bone mass loss and bone¿s limited self-regeneration is a major focus of research, emphasizing new biomaterials and cell therapy. Tissue bioengineering emerges as a potential alternative to conventional treatments. In this study, an experimental model of a critical bone lesion in rats was used to investigate bone regeneration by treating the defect with biomaterials Evolution® and Gen-Os® (OsteoBiol®, Turín, Italy), with or without mesenchymal stromal cells from dental pulp (DP-MSCs). Methods: Forty-six adult male Wistar rats were subjected to a 5-mm critical bone defect in the right mandible, which does not regenerate without intervention. The rats were randomly assigned to a Simulated Group, Control Group, or two Study Groups (using Evolution®, Gen-Os®, and DP-MSCs). The specimens were euthanized at three or six months, and radiological, histological, and ELISA tests were conducted to assess bone regeneration. Results: The radiological results showed that the DP-MSC group achieved uniform radiopacity and continuity in the bone edge, with near-complete structural defect restitution. Histologically, full bone regeneration was observed, with well-organized, vascularized lamellar bone and no lesion edges. These findings were supported by increases in endoglin, transforming growth factor-beta 1 (TGF-ß1), protocollagen, parathormone, and calcitonin, indicating a conducive environment for bone regeneration. Conclusions: The use of DP-MSCs combined with biomaterials with appropriate three-dimensional matrices is a promising therapeutic option for further exploration.