Periapical lesion-derived decellularized extracellular matrix as a potential solution for regenerative endodontics

Abstract Pulp regeneration remains a crucial target in the preservation of natural dentition. Using decellularized extracellular matrix is an appropriate approach to mimic natural microenvironment and facilitate tissue regeneration. In this study, we attempted to obtain decellularized extracellular...

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Published inRegenerative biomaterials Vol. 11; p. rbae050
Main Authors Hu, Nan, Jiang, Ruixue, Deng, Yuwei, Li, Weiping, Jiang, Wentao, Xu, Ningwei, Wang, Jia, Wen, Jin, Gu, Shensheng
Format Journal Article
LanguageEnglish
Published England Oxford University Press 07.05.2024
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Summary:Abstract Pulp regeneration remains a crucial target in the preservation of natural dentition. Using decellularized extracellular matrix is an appropriate approach to mimic natural microenvironment and facilitate tissue regeneration. In this study, we attempted to obtain decellularized extracellular matrix from periapical lesion (PL-dECM) and evaluate its bioactive effects. The decellularization process yielded translucent and viscous PL-dECM, meeting the standard requirements for decellularization efficiency. Proteomic sequencing revealed that the PL-dECM retained essential extracellular matrix components and numerous bioactive factors. The PL-dECM conditioned medium could enhance the proliferation and migration ability of periapical lesion-derived stem cells (PLDSCs) in a dose-dependent manner. Culturing PLDSCs on PL-dECM slices improved odontogenic/angiogenic ability compared to the type I collagen group. In vivo, the PL-dECM demonstrated a sustained supportive effect on PLDSCs and promoted odontogenic/angiogenic differentiation. Both in vitro and in vivo studies illustrated that PL-dECM served as an effective scaffold for pulp tissue engineering, providing valuable insights into PLDSCs differentiation. These findings pave avenues for the clinical application of dECM’s in situ transplantation for regenerative endodontics. Graphical abstract
Bibliography:Nan Hu and Ruixue Jiang authors contributed equally to this work.
ISSN:2056-3418
2056-3426
2056-3426
DOI:10.1093/rb/rbae050