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人牙细胞损伤后释放的血管生成生长因子的定量分析。

Quantification of angiogenic growth factors released by human dental cells after injury.

作者信息

Tran-Hung L, Laurent P, Camps J, About I

机构信息

Laboratoire IMEB-ERT 30, Faculté d'Odontologie, Université de la Méditerranée, 27 Boulevard Jean Moulin, 13355 Marseille Cedex 05, France.

出版信息

Arch Oral Biol. 2008 Jan;53(1):9-13. doi: 10.1016/j.archoralbio.2007.07.001. Epub 2007 Aug 30.

Abstract

OBJECTIVE

Angiogenesis is a key step in the dental pulp healing sequence which involves the dentine bridge formation. In a previous work, we showed that dental pulp cells secrete soluble factors which interact with endothelial cells and affect the process of angiogenesis. The objective of this work was to quantify the angiogenic growth factors released by mechanically injured human dental pulp cells and the effect of 2-hydroxyethyl methacrylate (HEMA) on this secretion.

DESIGN

Pulp cells were prepared from immature third molars explants by the outgrowth method. Cell monolayers were either subjected to mechanical injuries or treated with increasing concentrations of HEMA. ELISA was used to quantify the secreted angiogenic growth factors in the culture media after different time periods of injury and after incubation with different concentrations of HEMA.

RESULTS

Pulp cells secreted significant levels of PDGF-AB, VEGF and FGF-2. The concentration of these factors increased shortly (5h) after injury and returned to initial values after 1 day. HEMA treatment increased VEGF secretion but decreased that of FGF-2 in a dose-dependent manner while it did not affect PDGF-AB level.

CONCLUSIONS

Dental pulp cells secrete angiogenic growth factors which play a pivotal role in angiogenesis which precedes the reparative dentine formation. PDGF-AB seems to play a major role because its level showed the highest increase in mechanically injured cells. The presence of HEMA affects both FGF-2 and VEGF levels and may partially explain the lack of dentine bridging after direct pulp capping with an adhesive system.

摘要

目的

血管生成是牙髓愈合过程中的关键步骤,涉及牙本质桥的形成。在先前的研究中,我们发现牙髓细胞分泌可与内皮细胞相互作用并影响血管生成过程的可溶性因子。本研究的目的是量化机械损伤的人牙髓细胞释放的血管生成生长因子,以及甲基丙烯酸羟乙酯(HEMA)对这种分泌的影响。

设计

采用组织块生长法从未成熟的第三磨牙外植体中制备牙髓细胞。细胞单层要么受到机械损伤,要么用浓度递增的HEMA处理。采用酶联免疫吸附测定法(ELISA)来量化损伤后不同时间段以及与不同浓度的HEMA孵育后培养基中分泌的血管生成生长因子。

结果

牙髓细胞分泌大量的血小板衍生生长因子AB(PDGF-AB)、血管内皮生长因子(VEGF)和成纤维细胞生长因子2(FGF-2)。这些因子的浓度在损伤后不久(5小时)升高,并在1天后恢复到初始值。HEMA处理以剂量依赖的方式增加VEGF的分泌,但降低FGF-2的分泌,而对PDGF-AB水平没有影响。

结论

牙髓细胞分泌血管生成生长因子,这些因子在修复性牙本质形成之前的血管生成中起关键作用。PDGF-AB似乎起主要作用,因为其水平在机械损伤的细胞中升高幅度最大。HEMA的存在影响FGF-2和VEGF水平,这可能部分解释了用粘结系统直接盖髓后牙本质桥形成失败的原因。

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