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环孢素A对牙龈成纤维细胞白细胞介素-6分泌的调节作用

Regulation of gingival fibroblast interleukin-6 secretion by cyclosporine A.

作者信息

Morton R S, Dongari-Bagtzoglou A I

机构信息

Division of Periodontics, Columbia University, School of Dental and Oral Surgery, New York, NY 10032, USA.

出版信息

J Periodontol. 1999 Dec;70(12):1464-71. doi: 10.1902/jop.1999.70.12.1464.

Abstract

BACKGROUND

Cyclosporine A (CsA) is a widely used immunosuppressant, with clinical applications ranging from organ transplants to chronic inflammatory diseases. One of the side effects associated with CsA treatment is the development of gingival overgrowth. Exuberant growth of connective tissue within the periodontium can result from hyperactivity of resident fibroblasts. Fibroblasts are capable of secreting interleukin-6 (IL-6), which has been shown to enhance proliferation as well as collagen and glycosaminoglycan synthesis by these cells. We tested the hypothesis that one of the pathogenetic mechanisms underlying CsA-induced fibrosis is an enhanced IL-6 secretion by gingival fibroblasts (GF) in response to this drug.

METHODS

The ability of CsA to upregulate GF IL-6 secretion alone or in combination with bacterial challenge or other inflammatory cytokines was tested in an in vitro system. Fibroblast cultures were established from systemically healthy gingival tissue donors and were challenged with CsA in the absence or presence of bacteria, IL-1beta, or tumor necrosis factor (TNF) alpha as co-stimulants. Nifedipine and phenytoin were also tested to further support findings with CsA. After 72 hours of incubation, culture supernatants were collected and analyzed for IL-6 content by ELISA.

RESULTS

We have shown that GF respond to CsA with an increase in IL-6 secretion. The magnitude of this response varies among cultures derived from different tissue donors. We have also demonstrated that GF IL-6 responses to bacterial challenge or TNFalpha are downregulated by CsA. However, CsA synergizes with IL-1beta to further upregulate IL-6 secretion, and this effect is shared by phenytoin and nifedipine.

CONCLUSIONS

We conclude that one of the pathogenetic mechanisms underlying drug-induced gingival overgrowth may be enhanced secretion of IL-6 by GF in response to these medications. This is the first report on direct and indirect effects of gingival overgrowth-related medications on GF IL-6 metabolism. This work will lay the foundation for future studies directed towards the development of prevention or treatment modalities for gingival overgrowth based on blocking the fibrogenic activities of IL-6 at the cellular level.

摘要

背景

环孢素A(CsA)是一种广泛应用的免疫抑制剂,临床应用范围从器官移植到慢性炎症性疾病。与CsA治疗相关的副作用之一是牙龈过度生长。牙周组织内结缔组织的过度生长可能源于驻留成纤维细胞的过度活跃。成纤维细胞能够分泌白细胞介素-6(IL-6),研究表明IL-6可增强这些细胞的增殖以及胶原蛋白和糖胺聚糖的合成。我们检验了这样一个假设,即CsA诱导纤维化的发病机制之一是牙龈成纤维细胞(GF)对这种药物的反应导致IL-6分泌增加。

方法

在体外系统中测试了CsA单独或与细菌攻击或其他炎性细胞因子联合上调GF IL-6分泌的能力。从全身健康的牙龈组织供体建立成纤维细胞培养物,并在不存在或存在细菌、IL-1β或肿瘤坏死因子(TNF)α作为共刺激剂的情况下用CsA进行刺激。还测试了硝苯地平和苯妥英以进一步支持CsA的研究结果。孵育72小时后,收集培养上清液并通过酶联免疫吸附测定(ELISA)分析IL-6含量。

结果

我们已经表明,GF对CsA的反应是IL-6分泌增加。这种反应的程度在来自不同组织供体的培养物中有所不同。我们还证明,CsA可下调GF对细菌攻击或TNFα的IL-6反应。然而,CsA与IL-1β协同作用以进一步上调IL-6分泌,并且苯妥英和硝苯地平也具有这种作用。

结论

我们得出结论,药物性牙龈过度生长的发病机制之一可能是GF对这些药物的反应导致IL-6分泌增加。这是关于牙龈过度生长相关药物对GF IL-6代谢的直接和间接影响的首次报道。这项工作将为未来基于在细胞水平阻断IL-6的纤维化活性来开发牙龈过度生长的预防或治疗方法的研究奠定基础。

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