Contribution of Bone Marrow-derived Cells to Reparative Dentinogenesis Using Bone Marrow Transplantation Model

被引:8
|
作者
Frozoni, Marcos [1 ]
Marques, Marcelo Rocha [2 ]
Hamasaki, Silvia Kaoru [1 ]
Mohara, Nelson Tsutomu [1 ]
Soares, Adriana de Jesus [3 ]
Zaia, Alexandre Augusto [3 ]
机构
[1] Inst Pesquisa Sao Leopoldo Mandic, Fac Sao Leopoldo Mandic, Area Endodontia, Campinas, SP, Brazil
[2] Univ Estadual Campinas, Piracicaba Dent Sch, Dept Morphol, Div Histol & Embryol, Piracicaba, SP, Brazil
[3] Univ Estadual Campinas, Piracicaba Dent Sch, Dept Restorat Dent, Div Endodont, Piracicaba, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bone marrow cells; bone marrow transplantation; dental pulp regeneration; dentin sialo-protein; green fluorescent protein; reparative dentin; MESENCHYMAL STEM-CELLS; MINERAL TRIOXIDE AGGREGATE; DENTAL-PULP; SIALOPROTEIN GENE; PROGENITOR CELLS; EXPRESSION; REGENERATION; OSTEOPONTIN; BIODENTINE; MTA;
D O I
10.1016/j.joen.2019.12.003
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: The aim of this study was to analyze the contribution of bone marrow-derived cells (BMDCs) to reparative dentinogenesis using bone marrow transplantation (BMT) and pulp capping as an in vivo model. Methods: A chimeric mouse model was created through the injection of BMDCs expressing green fluorescent protein (GFP+ BMDCs) from C57BU6 GFP+ transgenic donor mice into irradiated C57BL/6 wild-type recipient mice (GFP- mice). These GFP-chimeric mice (containing transplanted GFP+ BMDCs) were subjected to microscopic pulp exposure and capping with white mineral trioxide aggregate (n = 18) or Biodentine (Septodont, St Maur-des-Fosses, France) (n = 18) in the maxillary first molar. Maxillary arches from GFP- chimeric mice (with the capped tooth) were isolated and histologically processed 5 (n = 9) and 7 (n = 9) weeks after BMT. Confocal laser microscopy and immunohistochemical analysis were performed to assess the presence of GFP+ BMDCs and the expression of dentin sialoprotein, an odontoblast marker, for those cells contributing to reparative dentinogenesis in the dental pulp. Results: Confocal laser microscopic analyses evidenced the presence of GFP+ BMDCs in close association with reparative dentin synthesized at the site of pulp exposure in GFP- mice 5 and 7 weeks after BMT. Immunohistochemical analysis revealed that GFP+ BMDCs in close association with reparative dentin expressed DSP, suggesting the contribution of nonresident GFP+ BMDCs to reparative dentinogenesis. Conclusions: These data suggest the presence of nonresident BMDCs in reparative dentinogenesis and its contribution to dental pulp regeneration in the pulp healing process.
引用
收藏
页码:404 / 412
页数:9
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