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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750895/ https://www.ncbi.nlm.nih.gov/pubmed/33414903 http://dx.doi.org/10.1177/2041731420981672 |
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author | Lee, Dong Joon Miguez, Patricia Kwon, Jane Daniel, Renie Padilla, Ricardo Min, Samuel Zalal, Rahim Ko, Ching-Chang Shin, Hae Won |
author_facet | Lee, Dong Joon Miguez, Patricia Kwon, Jane Daniel, Renie Padilla, Ricardo Min, Samuel Zalal, Rahim Ko, Ching-Chang Shin, Hae Won |
author_sort | Lee, Dong Joon |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-7750895 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77508952021-01-06 Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration Lee, Dong Joon Miguez, Patricia Kwon, Jane Daniel, Renie Padilla, Ricardo Min, Samuel Zalal, Rahim Ko, Ching-Chang Shin, Hae Won J Tissue Eng Original Article 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. SAGE Publications 2020-12-17 /pmc/articles/PMC7750895/ /pubmed/33414903 http://dx.doi.org/10.1177/2041731420981672 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Lee, Dong Joon Miguez, Patricia Kwon, Jane Daniel, Renie Padilla, Ricardo Min, Samuel Zalal, Rahim Ko, Ching-Chang Shin, Hae Won Decellularized pulp matrix as scaffold for mesenchymal stem cell mediated bone regeneration |
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 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7750895/ https://www.ncbi.nlm.nih.gov/pubmed/33414903 http://dx.doi.org/10.1177/2041731420981672 |
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