Cargando…

Injectable cartilaginous template transformed BMSCs into vascularized bone

Regeneration of alveolar bone for dental implant remains a major issue, partifcularly for patients suffering from severe bone adsorption and irregular socket trauma. Recapitulating embryological development is becoming an attractive approach for engineer organ or three-dimensional tissues from stem...

Descripción completa

Detalles Bibliográficos
Autores principales: Feng, Xiaoke, Li, Zhiye, Wei, Jianhua, Feng, Zhihong, Wu, Wei, Zhao, Yimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973938/
https://www.ncbi.nlm.nih.gov/pubmed/29844536
http://dx.doi.org/10.1038/s41598-018-26472-8
_version_ 1783326711433134080
author Feng, Xiaoke
Li, Zhiye
Wei, Jianhua
Feng, Zhihong
Wu, Wei
Zhao, Yimin
author_facet Feng, Xiaoke
Li, Zhiye
Wei, Jianhua
Feng, Zhihong
Wu, Wei
Zhao, Yimin
author_sort Feng, Xiaoke
collection PubMed
description Regeneration of alveolar bone for dental implant remains a major issue, partifcularly for patients suffering from severe bone adsorption and irregular socket trauma. Recapitulating embryological development is becoming an attractive approach for engineer organ or three-dimensional tissues from stem cells. In this study, we aimed to develop an injectable “cartilaginous” graft with adequate mechanical resistance and ideal bone remodelling potential. The cartilaginous graft was composed of a particulate decellularised cartilage matrix (PDCM), chondrogenically primed bone mesenchymal stem cell (BMSC) bricks (CB), and enriched platelet-rich plasma (P) gel. In immunodeficient mice, we found that angiogenesis occurred quickly inside PDCM-CB-P constructs after implantation, thereby improving tissue survival and bone formation. In rabbit tibia bone defects around implants, we confirmed that CBs not only transformed into bone tissue rapidly, but also significantly promoted bone remodelling and replacement of PDCM, thus realising osseointegration of dental implants within 3 months. In conclusion, CBs exhibited the potential for endochondral ossification in vivo, and application of a cartilaginous template composed of PDCM, CB, and P provided a minimally-invasive, “free material residual” approach to regenerate alveolar bone tissues in vivo. This method could have applications in peri-implant bone regeneration.
format Online
Article
Text
id pubmed-5973938
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-59739382018-05-31 Injectable cartilaginous template transformed BMSCs into vascularized bone Feng, Xiaoke Li, Zhiye Wei, Jianhua Feng, Zhihong Wu, Wei Zhao, Yimin Sci Rep Article Regeneration of alveolar bone for dental implant remains a major issue, partifcularly for patients suffering from severe bone adsorption and irregular socket trauma. Recapitulating embryological development is becoming an attractive approach for engineer organ or three-dimensional tissues from stem cells. In this study, we aimed to develop an injectable “cartilaginous” graft with adequate mechanical resistance and ideal bone remodelling potential. The cartilaginous graft was composed of a particulate decellularised cartilage matrix (PDCM), chondrogenically primed bone mesenchymal stem cell (BMSC) bricks (CB), and enriched platelet-rich plasma (P) gel. In immunodeficient mice, we found that angiogenesis occurred quickly inside PDCM-CB-P constructs after implantation, thereby improving tissue survival and bone formation. In rabbit tibia bone defects around implants, we confirmed that CBs not only transformed into bone tissue rapidly, but also significantly promoted bone remodelling and replacement of PDCM, thus realising osseointegration of dental implants within 3 months. In conclusion, CBs exhibited the potential for endochondral ossification in vivo, and application of a cartilaginous template composed of PDCM, CB, and P provided a minimally-invasive, “free material residual” approach to regenerate alveolar bone tissues in vivo. This method could have applications in peri-implant bone regeneration. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5973938/ /pubmed/29844536 http://dx.doi.org/10.1038/s41598-018-26472-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Feng, Xiaoke
Li, Zhiye
Wei, Jianhua
Feng, Zhihong
Wu, Wei
Zhao, Yimin
Injectable cartilaginous template transformed BMSCs into vascularized bone
title Injectable cartilaginous template transformed BMSCs into vascularized bone
title_full Injectable cartilaginous template transformed BMSCs into vascularized bone
title_fullStr Injectable cartilaginous template transformed BMSCs into vascularized bone
title_full_unstemmed Injectable cartilaginous template transformed BMSCs into vascularized bone
title_short Injectable cartilaginous template transformed BMSCs into vascularized bone
title_sort injectable cartilaginous template transformed bmscs into vascularized bone
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5973938/
https://www.ncbi.nlm.nih.gov/pubmed/29844536
http://dx.doi.org/10.1038/s41598-018-26472-8
work_keys_str_mv AT fengxiaoke injectablecartilaginoustemplatetransformedbmscsintovascularizedbone
AT lizhiye injectablecartilaginoustemplatetransformedbmscsintovascularizedbone
AT weijianhua injectablecartilaginoustemplatetransformedbmscsintovascularizedbone
AT fengzhihong injectablecartilaginoustemplatetransformedbmscsintovascularizedbone
AT wuwei injectablecartilaginoustemplatetransformedbmscsintovascularizedbone
AT zhaoyimin injectablecartilaginoustemplatetransformedbmscsintovascularizedbone