Fiche publication


Date publication

février 2025

Journal

Scientific reports

Auteurs

Membres identifiés du Cancéropôle Est :
Dr GINDRAUX Florelle


Tous les auteurs :
Galvez P, Ahmed Omar N, Siadous R, Durand M, Comperat L, Lafarge X, Gindraux F, Sentilhes L, Fricain JC, L'Heureux N, Fenelon M

Résumé

Thanks to its unique biological properties, the human amniotic membrane (AM) has shown promising results for guided bone regeneration (GBR), but displays some limitations such as poor space-maintaining ability. This study thus aimed to develop a new amnion/chorion membrane (ACM), with better mechanical properties as well as comparable or improved biological properties for GBR. We first developed a new decellularization method of ACM (DL-ACM) which was validated by DNA staining and quantification, and its cytocompatibility was established in vitro. The thickness of DL-ACM was significantly increased over thirty-fivefold, and its tearing strength and compression strength significantly increased more than tenfold compared to the decellularized AM (DL-AM). In vivo, DL-ACM demonstrated its biocompatibility subcutaneously, and its osteogenic properties were compared to DL-AM and a gold standard membrane in a GBR defect model in rats. Micro-CT and histomorphometric analysis showed that DL-ACM significantly promoted early bone regeneration after 1 week and significantly increased bone regeneration compared to the empty defect and the gold standard membrane over time. In this study, we developed a simple and reproducible method to produce an acellular, non-cytotoxic, and biocompatible DL-ACM. This new membrane is as effective as AM to promote early bone regeneration while demonstrating better biomechanical properties.

Mots clés

Acellular scaffold, Amniochorionic membrane, Amnion-chorion, Decellularization, Guided bone regeneration, In vivo, Placental membranes

Référence

Sci Rep. 2025 02 14;15(1):5483