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Epidermal growth factor in clinical practice - a review of its biological actions, clinical indications and safety implications.表皮生长因子在临床实践中的应用——综述其生物学作用、临床适应证和安全性影响。
Int Wound J. 2009 Oct;6(5):331-46. doi: 10.1111/j.1742-481X.2009.00622.x.
2
The effect of mineral trioxide aggregate on the mineralization ability of rat dental pulp cells: an in vitro study.三氧化矿物凝聚体对大鼠牙髓细胞矿化能力的影响:一项体外研究。
J Endod. 2008 Sep;34(9):1057-60. doi: 10.1016/j.joen.2008.06.007. Epub 2008 Jul 26.
3
Mineral trioxide aggregate material use in endodontic treatment: a review of the literature.矿物三氧化物凝聚体材料在牙髓病治疗中的应用:文献综述
Dent Mater. 2008 Feb;24(2):149-64. doi: 10.1016/j.dental.2007.04.007. Epub 2007 Jun 21.
4
Effects of growth factors on dental pulp cell sensitivity to amalgam toxicity.生长因子对牙髓细胞对汞合金毒性敏感性的影响。
Dent Mater. 2007 Oct;23(10):1205-10. doi: 10.1016/j.dental.2006.11.003. Epub 2006 Dec 27.
5
Induction of transforming growth factor-beta 1 on dentine pulp cells in different culture patterns.不同培养模式下牙本质牙髓细胞中转化生长因子-β1的诱导作用
Cell Biol Int. 2006 Apr;30(4):295-300. doi: 10.1016/j.cellbi.2005.12.001. Epub 2006 Feb 7.
6
Tissue engineering in endodontics.牙髓病学中的组织工程
Aust Endod J. 2005 Dec;31(3):111-3. doi: 10.1111/j.1747-4477.2005.tb00317.x.
7
FGF-2 potently induces both proliferation and DSP expression in collagen type I gel cultures of adult incisor immature pulp cells.成纤维细胞生长因子-2(FGF-2)能有效诱导成年切牙未成熟牙髓细胞在I型胶原凝胶培养物中的增殖和牙本质涎磷蛋白(DSP)表达。
Biochem Biophys Res Commun. 2004 Dec 17;325(3):1052-9. doi: 10.1016/j.bbrc.2004.10.136.
8
The use of recombinant human bone morphogenetic protein-2 (rhBMP-2) in orthopaedic applications.重组人骨形态发生蛋白-2(rhBMP-2)在骨科应用中的使用。
Expert Opin Biol Ther. 2004 May;4(5):741-8. doi: 10.1517/14712598.4.5.741.
9
The future role of a molecular approach to pulp-dentinal regeneration.分子方法在牙髓牙本质再生中的未来作用。
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10
Acceleration effect of human recombinant bone morphogenetic protein-2 on differentiation of human pulp cells into odontoblasts.人重组骨形态发生蛋白-2对人牙髓细胞向成牙本质细胞分化的促进作用。
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流动线、Durafill VS 和 Dycal 对牙髓细胞的毒性:生长因子的影响。

Toxicity of Flow Line, Durafill VS, and Dycal to dental pulp cells: effects of growth factors.

机构信息

Department of Biomedical Sciences, Marquette University, Milwaukee, WI 53233, USA.

出版信息

J Endod. 2010 Jul;36(7):1149-53. doi: 10.1016/j.joen.2010.03.013. Epub 2010 Apr 9.

DOI:10.1016/j.joen.2010.03.013
PMID:20630288
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2907173/
Abstract

INTRODUCTION

The objective was to determine the effects of growth factor treatment on dental pulp cell sensitivity to toxicity of 2 composite restoration materials, Flow Line and Durafill VS, and a calcium hydroxide pulp capping material, Dycal.

METHODS

Toxicity of the dental materials to cultures of primary dental pulp cells was determined by the MTT metabolism assay. The ability of 6 different growth factors to influence the toxicity was tested.

RESULTS

A 24-hour exposure to either Flow Line or Durafill VS caused approximately 40% cell death, whereas Dycal exposure caused approximately 80% cell death. The toxicity of Flow Line and Durafill VS was mediated by oxidative stress. Four of the growth factors tested (bone morphogenetic protein [BMP]-2, BMP-7, epidermal growth factor [EGF], and transforming growth factor [TGF]-beta) decreased the basal MTT values while making the cells resistant to Flow Line and Durafill VS toxicity except BMP-2, which made the cells more sensitive to Flow Line. Treatment with fibroblast growth factor-2 caused no change in basal MTT metabolism, prevented the toxicity of Durafill VS, but increased the toxicity of Flow Line. Treatment with insulin-like growth factor-I (IGF-I) increased basal MTT metabolism and made the cells resistant to Flow Line and Durafill VS toxicity. None of the growth factors made the cells resistant to Dycal toxicity.

CONCLUSIONS

The results indicated that growth factors can be used to alter the sensitivity of dental pulp cells to commonly used restoration materials. The growth factors BMP-7, EGF, TGF-beta, and IGF-I provided the best profile of effects, making the cells resistant to both Flow Line and Durafill VS toxicity.

摘要

简介

本研究旨在探讨生长因子处理对牙髓细胞敏感性的影响,研究对象为两种复合修复材料(Flow Line 和 Durafill VS)和一种氢氧化钙盖髓材料(Dycal)。

方法

通过 MTT 代谢测定法,检测牙髓细胞对牙科材料的毒性。测试了 6 种不同生长因子对毒性的影响。

结果

Flow Line 或 Durafill VS 暴露 24 小时后,细胞死亡率约为 40%,而 Dycal 暴露后细胞死亡率约为 80%。Flow Line 和 Durafill VS 的毒性是由氧化应激介导的。在测试的 4 种生长因子(骨形态发生蛋白[BMP]-2、BMP-7、表皮生长因子[EGF]和转化生长因子[TGF]-β)中,有 4 种生长因子(BMP-2、BMP-7、EGF 和 TGF-β)降低了基础 MTT 值,同时使细胞对 Flow Line 和 Durafill VS 的毒性具有抗性,而 BMP-2 则使细胞对 Flow Line 更敏感。碱性成纤维细胞生长因子-2(fibroblast growth factor-2)处理对基础 MTT 代谢没有影响,可防止 Durafill VS 的毒性,但增加了 Flow Line 的毒性。胰岛素样生长因子-I(IGF-I)处理增加了基础 MTT 代谢,使细胞对 Flow Line 和 Durafill VS 的毒性具有抗性。没有一种生长因子能使细胞对 Dycal 的毒性产生抗性。

结论

结果表明,生长因子可用于改变牙髓细胞对常用修复材料的敏感性。生长因子 BMP-7、EGF、TGF-β和 IGF-I 的效果最佳,使细胞对 Flow Line 和 Durafill VS 的毒性均具有抗性。