The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration

Adequate vascularization, a restricting factor for the survival of engineered tissues, is often promoted by the addition of stem cells or the appropriate angiogenic growth factors. In this study, human dental pulp stem cells (DPSCs) and stem cells from the apical papilla (SCAPs) were applied in an i...

Full description

Saved in:
Bibliographic Details
Main Authors: Petra Hilkens, Annelies Bronckaers, Jessica Ratajczak, Pascal Gervois, Esther Wolfs, Ivo Lambrichts
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2017/2582080
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832549995837915136
author Petra Hilkens
Annelies Bronckaers
Jessica Ratajczak
Pascal Gervois
Esther Wolfs
Ivo Lambrichts
author_facet Petra Hilkens
Annelies Bronckaers
Jessica Ratajczak
Pascal Gervois
Esther Wolfs
Ivo Lambrichts
author_sort Petra Hilkens
collection DOAJ
description Adequate vascularization, a restricting factor for the survival of engineered tissues, is often promoted by the addition of stem cells or the appropriate angiogenic growth factors. In this study, human dental pulp stem cells (DPSCs) and stem cells from the apical papilla (SCAPs) were applied in an in vivo model of dental pulp regeneration in order to compare their regenerative potential and confirm their previously demonstrated paracrine angiogenic properties. 3D-printed hydroxyapatite scaffolds containing DPSCs and/or SCAPs were subcutaneously transplanted into immunocompromised mice. After twelve weeks, histological and ultrastructural analysis demonstrated the regeneration of vascularized pulp-like tissue as well as mineralized tissue formation in all stem cell constructs. Despite the secretion of vascular endothelial growth factor in vitro, the stem cell constructs did not display a higher vascularization rate in comparison to control conditions. Similar results were found after eight weeks, which suggests both osteogenic/odontogenic differentiation of the transplanted stem cells and the promotion of angiogenesis in this particular setting. In conclusion, this is the first study to demonstrate the successful formation of vascularized pulp-like tissue in 3D-printed scaffolds containing dental stem cells, emphasizing the promising role of this approach in dental tissue engineering.
format Article
id doaj-art-4f409c210b274ca2919a49f2f6a64d33
institution Kabale University
issn 1687-966X
1687-9678
language English
publishDate 2017-01-01
publisher Wiley
record_format Article
series Stem Cells International
spelling doaj-art-4f409c210b274ca2919a49f2f6a64d332025-02-03T06:07:54ZengWileyStem Cells International1687-966X1687-96782017-01-01201710.1155/2017/25820802582080The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp RegenerationPetra Hilkens0Annelies Bronckaers1Jessica Ratajczak2Pascal Gervois3Esther Wolfs4Ivo Lambrichts5Laboratory of Morphology, Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, BelgiumLaboratory of Morphology, Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, BelgiumLaboratory of Morphology, Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, BelgiumLaboratory of Morphology, Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, BelgiumLaboratory of Morphology, Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, BelgiumLaboratory of Morphology, Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, BelgiumAdequate vascularization, a restricting factor for the survival of engineered tissues, is often promoted by the addition of stem cells or the appropriate angiogenic growth factors. In this study, human dental pulp stem cells (DPSCs) and stem cells from the apical papilla (SCAPs) were applied in an in vivo model of dental pulp regeneration in order to compare their regenerative potential and confirm their previously demonstrated paracrine angiogenic properties. 3D-printed hydroxyapatite scaffolds containing DPSCs and/or SCAPs were subcutaneously transplanted into immunocompromised mice. After twelve weeks, histological and ultrastructural analysis demonstrated the regeneration of vascularized pulp-like tissue as well as mineralized tissue formation in all stem cell constructs. Despite the secretion of vascular endothelial growth factor in vitro, the stem cell constructs did not display a higher vascularization rate in comparison to control conditions. Similar results were found after eight weeks, which suggests both osteogenic/odontogenic differentiation of the transplanted stem cells and the promotion of angiogenesis in this particular setting. In conclusion, this is the first study to demonstrate the successful formation of vascularized pulp-like tissue in 3D-printed scaffolds containing dental stem cells, emphasizing the promising role of this approach in dental tissue engineering.http://dx.doi.org/10.1155/2017/2582080
spellingShingle Petra Hilkens
Annelies Bronckaers
Jessica Ratajczak
Pascal Gervois
Esther Wolfs
Ivo Lambrichts
The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration
Stem Cells International
title The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration
title_full The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration
title_fullStr The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration
title_full_unstemmed The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration
title_short The Angiogenic Potential of DPSCs and SCAPs in an In Vivo Model of Dental Pulp Regeneration
title_sort angiogenic potential of dpscs and scaps in an in vivo model of dental pulp regeneration
url http://dx.doi.org/10.1155/2017/2582080
work_keys_str_mv AT petrahilkens theangiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT anneliesbronckaers theangiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT jessicaratajczak theangiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT pascalgervois theangiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT estherwolfs theangiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT ivolambrichts theangiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT petrahilkens angiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT anneliesbronckaers angiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT jessicaratajczak angiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT pascalgervois angiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT estherwolfs angiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration
AT ivolambrichts angiogenicpotentialofdpscsandscapsinaninvivomodelofdentalpulpregeneration