Gavrila Adelina, Chachi Latifa, Tliba Omar, Brightling Christopher, Amrani Yassine
1 Department of Infection, Immunity and Inflammation, University of Leicester, Leicester, United Kingdom; and.
2 Department of Pharmaceutical Sciences, Thomas Jefferson University, Jefferson School of Pharmacy, Philadelphia, Pennsylvania.
Am J Respir Cell Mol Biol. 2015 Nov;53(5):728-37. doi: 10.1165/rcmb.2014-0477OC.
Preclinical models of human conditions including asthma showed the therapeutic potential of Compound A (CpdA), a dissociated glucocorticoid (GC) receptor (GRα) ligand. Whether CpdA inhibits GC resistance, a central feature of severe asthma, has not been addressed. We investigated whether CpdA modulates cytokine-induced GC resistance in human airway smooth muscle (ASM) cells. Healthy and asthmatic ASM cells were treated with TNF-α/IFN-γ for 24 hours in the presence or absence of CpdA. ELISA and quantitative PCR assays were used to assess the effect of CpdA on chemokine expression. Activation of GRα by CpdA was assessed by quantitative PCR, immunostaining, and receptor antagonism using RU486. An effect of CpdA on the transcription factor interferon regulatory factor 1 (IRF-1) was investigated using immunoblot, immunostaining, and small interfering RNA (siRNA) knockdown. CpdA inhibited production of fluticasone-resistant chemokines CCL5, CX3CL1, and CXCL10 at protein and mRNA levels in both asthmatic and healthy cells. CpdA failed to induce expression of GC-induced Leucine Zipper while transiently inducing mitogen-activated protein kinase phosphatase 1 (MKP-1) at both mRNA and protein levels. CpdA inhibitory action was not associated with GRα nuclear translocation, nor was it prevented by RU486 antagonism. Activation of IRF-1 by TNF-α/IFN-γ was inhibited by CpdA. IRF-1 siRNA knockdown reduced cytokine-induced CCL5 and CX3CL1 production. siRNA MKP-1 prevented the inhibitory effect of CpdA on cytokine-induced CXCL10 production. For the first time, we show that CpdA inhibits the production of GC-resistant chemokines via GRα-independent mechanisms involving the inhibition of IRF-1 and up-regulation of MKP-1. Thus, targeting CpdA-sensitive pathways in ASM cells represents an alternative therapeutic approach to treat GC resistance in asthma.
包括哮喘在内的人类疾病的临床前模型显示了化合物A(CpdA)的治疗潜力,CpdA是一种解离的糖皮质激素(GC)受体(GRα)配体。CpdA是否能抑制GC抵抗(重度哮喘的一个主要特征)尚未得到研究。我们研究了CpdA是否能调节人气道平滑肌(ASM)细胞中细胞因子诱导的GC抵抗。在有或没有CpdA的情况下,用TNF-α/IFN-γ处理健康和哮喘ASM细胞24小时。采用ELISA和定量PCR分析评估CpdA对趋化因子表达的影响。通过定量PCR、免疫染色以及使用RU486进行受体拮抗来评估CpdA对GRα的激活作用。使用免疫印迹、免疫染色和小干扰RNA(siRNA)敲低技术研究了CpdA对转录因子干扰素调节因子1(IRF-1)的影响。CpdA在蛋白质和mRNA水平上抑制了哮喘和健康细胞中对氟替卡松耐药的趋化因子CCL5、CX3CL1和CXCL10的产生。CpdA未能诱导GC诱导的亮氨酸拉链的表达,同时在mRNA和蛋白质水平上短暂诱导丝裂原活化蛋白激酶磷酸酶1(MKP-1)。CpdA的抑制作用与GRα核转位无关,也不能被RU486拮抗所阻止。CpdA抑制了TNF-α/IFN-γ对IRF-1的激活。IRF-1 siRNA敲低减少了细胞因子诱导的CCL5和CX3CL1的产生。siRNA MKP-1阻止了CpdA对细胞因子诱导的CXCL10产生的抑制作用。我们首次表明,CpdA通过不依赖GRα的机制抑制GC耐药趋化因子的产生,该机制涉及对IRF-1的抑制和MKP-1的上调。因此,针对ASM细胞中对CpdA敏感的途径代表了一种治疗哮喘中GC抵抗的替代治疗方法。