Potential dental pulp revascularization and odonto-/osteogenic capacity of a novel transplant combined with dental pulp stem cells and platelet-rich fibrin

被引:70
作者
Chen, Yong-Jin [1 ]
Zhao, Yin-Hua [1 ]
Zhao, Ya-Juan [1 ]
Liu, Nan-Xia [1 ]
Lv, Xin [1 ]
Li, Qiang [1 ]
Chen, Fa-Ming [2 ]
Zhang, Min [1 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Dept Gen Dent & Emergency, State Key Lab Mil Stomatol, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Sch Stomatol, Dept Periodontol & Oral Med, State Key Lab Mil Stomatol, Xian 710032, Peoples R China
基金
中国国家自然科学基金;
关键词
Pulp revascularization; Dental pulp stem cells; Platelet-rich fibrin; Cell sheets; Regenerative dentistry; CHRONIC APICAL ABSCESS; MATRIX PROTEIN-1; BONE-MARROW; IN-VITRO; ALKALINE-PHOSPHATASE; PERMANENT TOOTH; REGENERATION; TISSUE; DIFFERENTIATION; PROLIFERATION;
D O I
10.1007/s00441-015-2125-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Our aim is to investigate the cytobiological effects of autologous platelet-rich fibrin (PRF) on dental pulp stem cells (DPSCs) and to explore the ectopic and orthotopic possibilities of dental pulp revascularization and pulp-dentin complex regeneration along the root canal cavities of the tooth by using a novel tissue-engineered transplant composed of cell-sheet fragments of DPSCs and PRF granules. Canine DPSCs were isolated and characterized by assaying their colony-forming ability and by determining their cell surface markers and osteogenic/adipogenic differentiation potential. The biological effects of autologous PRF on DPSCs, including cell proliferation, alkaline phosphatase (ALP) activity and odonto-/osteogenic gene expression, were then investigated and quantified. A novel transplant consisting of cell-sheet fragments of DPSCs and PRF granules was adopted to regenerate pulp-dentin-like tissues in the root canal, both subcutaneously in nude mice and in the roots of canines. PRF promoted the proliferation of DPSCs in a dose-and time-dependent manner and induced the differentiation of DPSCs to odonto-/osteoblastic fates by increasing the expression of the Alp, Dspp, Dmp1 and Bsp genes. Transplantation of the DPSC/PRF construct led both to a favorable regeneration of homogeneous and compact pulp-like tissues with abundantly distributed blood capillaries and to the deposition of regenerated dentin along the intracanal walls at 8 weeks post-operation. Thus, the application of DPSC/PRF tissue constructs might serve as a potential therapy in regenerative endodontics for pulp revitalization or revascularization.
引用
收藏
页码:439 / 455
页数:17
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