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PPARγ激活剂对人支气管上皮细胞中MMP - 9表达的抑制作用。

Inhibition of MMP-9 expression by PPARgamma activators in human bronchial epithelial cells.

作者信息

Hetzel M, Walcher D, Grüb M, Bach H, Hombach V, Marx N

机构信息

Department of Internal Medicine II, University of Ulm, Robert-Koch-Strasse 8, D-89081 Ulm, Germany.

出版信息

Thorax. 2003 Sep;58(9):778-83. doi: 10.1136/thorax.58.9.778.

Abstract

BACKGROUND

The release of matrix degrading enzymes such as matrix metalloproteinase 9 (MMP-9) from bronchial epithelial cells is critically involved in airway wall remodelling in chronic inflammatory processes of the respiratory system. MMP-9 expression is induced by inflammatory mediators such as tumour necrosis factor (TNF)-alpha, but to date nothing is known about the mechanisms of inhibition of MMP-9 expression in these cells.

METHODS

A study was undertaken to examine whether activators of the nuclear transcription factor peroxisome proliferator activated receptor gamma (PPARgamma) might modulate MMP-9 expression in two different bronchial epithelial cell lines.

RESULTS

PPARgamma was expressed and was functionally active in NL20 and BEAS cells. Activation of PPARgamma by rosiglitazone or pioglitazone significantly reduced TNF-alpha and PMA induced MMP-9 gelatinolytic activity in a concentration dependent manner in both cell lines, but did not alter the expression of tissue inhibitor of MMPs type 1 (TIMP-1), the local inhibitor of MMP-9. Northern blot analysis revealed a decrease in MMP-9 mRNA expression following treatment with PPARgamma which resulted from the inhibition of NF-kappaB activation in these cells, as determined by transient transfection assays and electromobility shift assays.

CONCLUSION

Activation of PPARgamma in human bronchial epithelial cells limits the expression of matrix degrading MMP-9. This might have therapeutic applications in chronic inflammatory processes of the respiratory system.

摘要

背景

支气管上皮细胞释放基质降解酶,如基质金属蛋白酶9(MMP - 9),在呼吸系统慢性炎症过程中的气道壁重塑中起关键作用。MMP - 9的表达由炎症介质如肿瘤坏死因子(TNF)-α诱导,但迄今为止,关于这些细胞中MMP - 9表达的抑制机制尚不清楚。

方法

进行了一项研究,以检查核转录因子过氧化物酶体增殖物激活受体γ(PPARγ)的激活剂是否可能调节两种不同支气管上皮细胞系中的MMP - 9表达。

结果

PPARγ在NL20和BEAS细胞中表达且具有功能活性。罗格列酮或吡格列酮激活PPARγ以浓度依赖性方式显著降低了两种细胞系中TNF -α和佛波酯(PMA)诱导的MMP - 9明胶酶活性,但未改变MMP - 9的局部抑制剂基质金属蛋白酶组织抑制剂1(TIMP - 1)的表达。Northern印迹分析显示,用PPARγ处理后MMP - 9 mRNA表达降低,这是由于这些细胞中核因子κB(NF -κB)激活受到抑制,这通过瞬时转染试验和电泳迁移率变动分析确定。

结论

人支气管上皮细胞中PPARγ的激活限制了基质降解酶MMP - 9的表达。这可能在呼吸系统慢性炎症过程中具有治疗应用。

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