Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration

Scaffolds that are used for bone repair should provide an adequate environment for biomineralization by mesenchymal stem cells (MSCs). Recently, decellularized pulp matrices (DPM) have been utilized in endodontics for their high regenerative potential. Inspired by the dystrophic calcification on the...

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Main Authors: Dong Joon Lee, Patricia Miguez, Jane Kwon, Renie Daniel, Ricardo Padilla, Samuel Min, Rahim Zalal, Ching-Chang Ko, Hae Won Shin
Format: Article
Language:English
Published: SAGE Publishing 2020-12-01
Series:Journal of Tissue Engineering
Online Access:https://doi.org/10.1177/2041731420981672
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author Dong Joon Lee
Patricia Miguez
Jane Kwon
Renie Daniel
Ricardo Padilla
Samuel Min
Rahim Zalal
Ching-Chang Ko
Hae Won Shin
author_facet Dong Joon Lee
Patricia Miguez
Jane Kwon
Renie Daniel
Ricardo Padilla
Samuel Min
Rahim Zalal
Ching-Chang Ko
Hae Won Shin
author_sort Dong Joon Lee
collection DOAJ
description Scaffolds that are used for bone repair should provide an adequate environment for biomineralization by mesenchymal stem cells (MSCs). Recently, decellularized pulp matrices (DPM) have been utilized in endodontics for their high regenerative potential. Inspired by the dystrophic calcification on the pulp matrix known as pulp stone, we developed acellular pulp bioscaffolds and examined their potential in facilitating MSCs mineralization for bone defect repair. Pulp was decellularized, then retention of its structural integrity was confirmed by histological, mechanical, and biochemical evaluations. MSCs were seeded and proliferation, osteogenic gene expression, and biomineralization were assessed to verify DPM’s osteogenic effects in vitro. MicroCT, energy-dispersive X-ray (EDX), and histological analyses were used to confirm that DPM seeded with MSCs result in greater mineralization on rat critical-sized defects than that without MSCs. Overall, our study proves DPM’s potential to serve as a scaffolding material for MSC-mediated bone regeneration for future craniofacial bone tissue engineering.
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spelling doaj.art-ad2c38ec863d4754af7851c002aa07752022-12-21T21:30:54ZengSAGE PublishingJournal of Tissue Engineering2041-73142020-12-011110.1177/2041731420981672Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regenerationDong Joon Lee0Patricia Miguez1Jane Kwon2Renie Daniel3Ricardo Padilla4Samuel Min5Rahim Zalal6Ching-Chang Ko7Hae Won Shin8Oral and Craniofacial Health Science Institute, School of Dentistry, University of North Carolina, Chapel Hill, NC, USADepartment of Periodontics, School of Dentistry, University of North Carolina, Chapel Hill, NC, USADepartment of Neurology and Neurosurgery, School of Medicine, University of North Carolina, Chapel Hill, NC, USADepartment of Oral and Maxillofacial Surgery, School of Dentistry, University of North Carolina, Chapel Hill, NC, USADepartment of Diagnostic Sciences, School of Dentistry, University of North Carolina, Chapel Hill, NC, USAOral and Craniofacial Health Science Institute, School of Dentistry, University of North Carolina, Chapel Hill, NC, USAOral and Craniofacial Health Science Institute, School of Dentistry, University of North Carolina, Chapel Hill, NC, USADepartment of Orthodontics, School of Dentistry, University of North Carolina, Chapel Hill, NC, USADepartment of Neurology and Neurosurgery, School of Medicine, University of North Carolina, Chapel Hill, NC, USAScaffolds that are used for bone repair should provide an adequate environment for biomineralization by mesenchymal stem cells (MSCs). Recently, decellularized pulp matrices (DPM) have been utilized in endodontics for their high regenerative potential. Inspired by the dystrophic calcification on the pulp matrix known as pulp stone, we developed acellular pulp bioscaffolds and examined their potential in facilitating MSCs mineralization for bone defect repair. Pulp was decellularized, then retention of its structural integrity was confirmed by histological, mechanical, and biochemical evaluations. MSCs were seeded and proliferation, osteogenic gene expression, and biomineralization were assessed to verify DPM’s osteogenic effects in vitro. MicroCT, energy-dispersive X-ray (EDX), and histological analyses were used to confirm that DPM seeded with MSCs result in greater mineralization on rat critical-sized defects than that without MSCs. Overall, our study proves DPM’s potential to serve as a scaffolding material for MSC-mediated bone regeneration for future craniofacial bone tissue engineering.https://doi.org/10.1177/2041731420981672
spellingShingle Dong Joon Lee
Patricia Miguez
Jane Kwon
Renie Daniel
Ricardo Padilla
Samuel Min
Rahim Zalal
Ching-Chang Ko
Hae Won Shin
Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
Journal of Tissue Engineering
title Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
title_full Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
title_fullStr Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
title_full_unstemmed Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
title_short Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
title_sort decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration
url https://doi.org/10.1177/2041731420981672
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