Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair

Bioactive growth factors identified within the extracellular matrix of dentine have been proposed roles in regulating the naturally inherent regenerative dentine formation seen in teeth in response to trauma and infection, which may also be harnessed for novel clinical treatments in augmenting miner...

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Main Authors: Chi P Lee, John S Colombo, Wayne Nishio Ayre, Alastair J Sloan, Rachel J Waddington
Format: Article
Language:English
Published: SAGE Publishing 2015-05-01
Series:Journal of Tissue Engineering
Online Access:https://doi.org/10.1177/2041731415586318
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spelling doaj-eec066d616634bf796a0336390ba111d2020-11-25T03:33:15ZengSAGE PublishingJournal of Tissue Engineering2041-73142015-05-01610.1177/204173141558631810.1177_2041731415586318Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repairChi P Lee0John S Colombo1Wayne Nishio Ayre2Alastair J Sloan3Rachel J Waddington4Department of Medicine, Imperial College London, London, UKSchool of Dentistry, The University of Utah, Salt Lake City, UT, USACardiff Institute of Tissue Engineering and Repair, Cardiff University, Cardiff, UKCardiff Institute of Tissue Engineering and Repair, Cardiff University, Cardiff, UKCardiff Institute of Tissue Engineering and Repair, Cardiff University, Cardiff, UKBioactive growth factors identified within the extracellular matrix of dentine have been proposed roles in regulating the naturally inherent regenerative dentine formation seen in teeth in response to trauma and infection, which may also be harnessed for novel clinical treatments in augmenting mineralised tissue repair. This study examined the specific biological action of demineralised dentine matrix extract on a clonal population of dental pulp stem cells in stimulating the prerequisite stages of wound healing associated with mineralised tissue repair. A clonal dental pulp stem cell population with sustained proliferative capacity and multi-potentiality towards osteogenic, adipogenic and chondrogenic lineages was isolated from the pulp of human third molars. Dentine was collected from human healthy teeth, powdered and treated with ethylenediaminetetraacetic acid to obtain a solubilised DDM protein extract. The influence of DDM on the DPSC clonal population was assessed in vitro. Exposure of cells to proteolytically degraded DDM or unsupplemented media served as controls. Compared to controls, DDM stimulated cell expansion, reduced apoptotic marker caspase 3, increased cell survival marker Akt1 and enhanced mineralised matrix deposition as determined by mineral deposition and increased expression of bone-related markers, alkaline phosphatase and osteopontin. Dental pulp stem cells successfully migrated into collagen gels supplemented with demineralised dentine matrix, with cells remaining viable and expanding in numbers over a 3-day period. Collectively, the results provide evidence that soluble proteins extracted from dentine matrix are able to exert a direct biological effect on dental pulp stem cells in promoting mineralised tissue repair mechanisms.https://doi.org/10.1177/2041731415586318
collection DOAJ
language English
format Article
sources DOAJ
author Chi P Lee
John S Colombo
Wayne Nishio Ayre
Alastair J Sloan
Rachel J Waddington
spellingShingle Chi P Lee
John S Colombo
Wayne Nishio Ayre
Alastair J Sloan
Rachel J Waddington
Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
Journal of Tissue Engineering
author_facet Chi P Lee
John S Colombo
Wayne Nishio Ayre
Alastair J Sloan
Rachel J Waddington
author_sort Chi P Lee
title Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
title_short Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
title_full Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
title_fullStr Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
title_full_unstemmed Elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
title_sort elucidating the cellular actions of demineralised dentine matrix extract on a clonal dental pulp stem cell population in orchestrating dental tissue repair
publisher SAGE Publishing
series Journal of Tissue Engineering
issn 2041-7314
publishDate 2015-05-01
description Bioactive growth factors identified within the extracellular matrix of dentine have been proposed roles in regulating the naturally inherent regenerative dentine formation seen in teeth in response to trauma and infection, which may also be harnessed for novel clinical treatments in augmenting mineralised tissue repair. This study examined the specific biological action of demineralised dentine matrix extract on a clonal population of dental pulp stem cells in stimulating the prerequisite stages of wound healing associated with mineralised tissue repair. A clonal dental pulp stem cell population with sustained proliferative capacity and multi-potentiality towards osteogenic, adipogenic and chondrogenic lineages was isolated from the pulp of human third molars. Dentine was collected from human healthy teeth, powdered and treated with ethylenediaminetetraacetic acid to obtain a solubilised DDM protein extract. The influence of DDM on the DPSC clonal population was assessed in vitro. Exposure of cells to proteolytically degraded DDM or unsupplemented media served as controls. Compared to controls, DDM stimulated cell expansion, reduced apoptotic marker caspase 3, increased cell survival marker Akt1 and enhanced mineralised matrix deposition as determined by mineral deposition and increased expression of bone-related markers, alkaline phosphatase and osteopontin. Dental pulp stem cells successfully migrated into collagen gels supplemented with demineralised dentine matrix, with cells remaining viable and expanding in numbers over a 3-day period. Collectively, the results provide evidence that soluble proteins extracted from dentine matrix are able to exert a direct biological effect on dental pulp stem cells in promoting mineralised tissue repair mechanisms.
url https://doi.org/10.1177/2041731415586318
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