Regenerative Endodontic Procedures: A Perspective from Stem Cell Niche Biology

被引:22
|
作者
Mari-Beffa, Manuel [1 ,2 ]
Jose Segura-Egea, Juan [3 ]
Diaz-Cuenca, Aranzazu [2 ,4 ]
机构
[1] Univ Malaga, Fac Sci, Dept Cell Biol Genet & Physiol, Malaga, Spain
[2] Univ Malaga, CIBER BBN, Networking Res Ctr Bioengn Biomat & Nanomed, Malaga, Spain
[3] Joint CSIC Univ Seville Ctr, Fac Dent, Dept Stomatol, Seville, Spain
[4] Joint CSIC Univ Seville Ctr, ICMS, Mat Sci Inst Seville, Seville, Spain
关键词
Biomaterial; endodontics; equivalence; regenerative endodontic procedures; stem cell niche; translational research; HUMAN DENTAL-PULP; PLATELET-RICH PLASMA; ROOT-CANAL SPACE; PHOSPHATE COMPOSITE SCAFFOLDS; COLONY-STIMULATING FACTOR; GROWTH-FACTOR-I; APICAL PERIODONTITIS; GENE-EXPRESSION; IMMATURE TEETH; BONE-MARROW;
D O I
10.1016/j.joen.2016.09.011
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: Endodontics uses cell therapy strategies to treat pulpal and periapical diseases. During these therapies, surgeons aim to reconstruct the natural microenvironments that regulate the activity of dental stem cells. Methods: We searched for more than 400 articles in PubMed using key words from regenerative endodontics and dental stem cell biology. In 268 articles, we reviewed what factors may influence histologic results after preclinical dental treatments that use regenerative endodontic procedures after pulpectomy. Results: Several factors, such as the origin of stem cells, the biomimicry of scaffolds used, and the size of lesions, are considered to influence the histologic appearance of the regenerated pulp-dentin complex after treatments. Information is accumulating on transcription factors that generate the pulp-dentin complex and survival/trophic factors that would benefit niche recovery and histologic results. Conclusions: In this article, we discuss the noninterchangeability of stem cells, the influence of dentin-entrapped molecule release on pulp regeneration and survival of stem cells, and the need of positional markers to assess treatments histologically. The ex vivo amplification of appropriate dental stem cells, the search for scaffolds storing the molecular diversity entrapped in the dentin, and the use of positional transcription factors as histologic markers are necessary to improve future preclinical experiments.
引用
收藏
页码:52 / 62
页数:11
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