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本文引用的文献

1
Dentonin, a MEPE fragment, initiates pulp-healing response to injury.牙本质涎磷蛋白片段丹通宁引发牙髓对损伤的愈合反应。
J Dent Res. 2007 Aug;86(8):780-5. doi: 10.1177/154405910708600818.
2
Amelogenin, a major structural protein in mineralizing enamel, is also expressed in soft tissues: brain and cells of the hematopoietic system.釉原蛋白是矿化牙釉质中的一种主要结构蛋白,在软组织(大脑和造血系统细胞)中也有表达。
Eur J Oral Sci. 2006 May;114 Suppl 1:183-9; discussion 201-2, 381. doi: 10.1111/j.1600-0722.2006.00301.x.
3
The impact of bioactive molecules to stimulate tooth repair and regeneration as part of restorative dentistry.生物活性分子作为修复牙科的一部分对刺激牙齿修复和再生的影响。
Dent Clin North Am. 2006 Apr;50(2):277-98, x. doi: 10.1016/j.cden.2005.11.008.
4
New cellular models for tracking the odontoblast phenotype.用于追踪成牙本质细胞表型的新型细胞模型。
Arch Oral Biol. 2005 Feb;50(2):271-7. doi: 10.1016/j.archoralbio.2004.10.007. Epub 2004 Dec 15.
5
Osteogenic proteins (bone sialoprotein and bone morphogenetic protein-7) and dental pulp mineralization.成骨蛋白(骨涎蛋白和骨形态发生蛋白-7)与牙髓矿化
J Mater Sci Mater Med. 2002 Feb;13(2):225-32. doi: 10.1023/a:1013846516693.
6
CELLS AND EXTRACELLULAR MATRICES OF DENTIN AND PULP: A BIOLOGICAL BASIS FOR REPAIR AND TISSUE ENGINEERING.牙本质和牙髓的细胞与细胞外基质:修复与组织工程的生物学基础
Crit Rev Oral Biol Med. 2004 Jan 1;15(1):13-27. doi: 10.1177/154411130401500103.
7
Bioactive molecules and the future of pulp therapy.生物活性分子与牙髓治疗的未来。
Am J Dent. 2003 Feb;16(1):66-76.
8
Application of bioactive molecules in pulp-capping situations.生物活性分子在盖髓术中的应用。
Adv Dent Res. 2001 Aug;15:91-5. doi: 10.1177/08959374010150012401.
9
Differential repair responses in the coronal and radicular areas of the exposed rat molar pulp induced by recombinant human bone morphogenetic protein 7 (osteogenic protein 1).重组人骨形态发生蛋白7(成骨蛋白1)诱导的暴露大鼠磨牙牙髓冠部和根部区域的差异修复反应
Arch Oral Biol. 2002 Mar;47(3):177-87. doi: 10.1016/s0003-9969(01)00100-5.
10
Bone sialoprotein-induced reparative dentinogenesis in the pulp of rat's molar.骨涎蛋白诱导大鼠磨牙牙髓中修复性牙本质形成
Clin Oral Investig. 2000 Jun;4(2):110-9. doi: 10.1007/s007840050126.

基质细胞分子和成牙本质细胞祖细胞作为牙本质修复和再生的工具。

Matricellular molecules and odontoblast progenitors as tools for dentin repair and regeneration.

作者信息

Goldberg M, Lacerda-Pinheiro S, Priam F, Jegat N, Six N, Bonnefoix M, Septier D, Chaussain-Miller C, Veis A, Denbesten P, Poliard A

机构信息

Laboratoire de Réparation et de Remodelages Oro-Faciaux (EA 2496), Université Paris Descartes, Montrouge, France.

出版信息

Clin Oral Investig. 2008 Jun;12(2):109-12. doi: 10.1007/s00784-007-0172-6. Epub 2007 Dec 22.

DOI:10.1007/s00784-007-0172-6
PMID:18157557
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2834229/
Abstract

This review summarizes the in vivo experiments carried out by our group after implantation of bioactive molecules (matricellular molecules) into the exposed pulp of the first maxillary molar of the rat or the mandibular incisor of rats and mice. We describe the cascade of recruitment, proliferation and terminal differentiation of cells involved in the formation of reparative dentin. Cloned immortalized odontoblast progenitors were also implanted in the incisors and in vitro studies aimed at revealing the signaling pathways leading from undifferentiated progenitors to fully differentiated polarized cells. Together, these experimental approaches pave the way for controlled dentin regenerative processes and repair.

摘要

本综述总结了我们小组进行的体内实验,这些实验是将生物活性分子(基质细胞分子)植入大鼠上颌第一磨牙或大鼠和小鼠下颌切牙的暴露牙髓后开展的。我们描述了参与修复性牙本质形成的细胞的募集、增殖和终末分化级联反应。克隆的永生化成牙本质细胞祖细胞也被植入切牙,并进行了体外研究,旨在揭示从未分化祖细胞到完全分化的极化细胞的信号通路。这些实验方法共同为可控的牙本质再生过程和修复铺平了道路。