Hetzel M, Walcher D, Grüb M, Bach H, Hombach V, Marx N
Department of Internal Medicine II, University of Ulm, Robert-Koch-Strasse 8, D-89081 Ulm, Germany.
Thorax. 2003 Sep;58(9):778-83. doi: 10.1136/thorax.58.9.778.
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.
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.
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.
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.
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。
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。
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。
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。