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Bronchial epithelial cells are rendered insensitive to glucocorticoid transactivation by transforming growth factor-β1.支气管上皮细胞对转化生长因子-β1介导的糖皮质激素转导作用不敏感。
Respir Res. 2014 May 1;15(1):55. doi: 10.1186/1465-9921-15-55.
2
Transcriptional and epigenetic modulation of human rhinovirus-induced CXCL10 production by cigarette smoke.香烟烟雾对人鼻病毒诱导的 CXCL10 产生的转录和表观遗传调节。
Am J Respir Cell Mol Biol. 2014 Mar;50(3):571-82. doi: 10.1165/rcmb.2013-0129OC.
3
Functional KCa3.1 channels regulate steroid insensitivity in bronchial smooth muscle cells.功能性 KCa3.1 通道调节支气管平滑肌细胞中的类固醇不敏感性。
J Immunol. 2013 Sep 1;191(5):2624-2636. doi: 10.4049/jimmunol.1300104. Epub 2013 Jul 31.
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Selective modulation of the glucocorticoid receptor can distinguish between transrepression of NF-κB and AP-1.选择性调节糖皮质激素受体可以区分 NF-κB 和 AP-1 的反式阻遏作用。
Cell Mol Life Sci. 2014 Jan;71(1):143-63. doi: 10.1007/s00018-013-1367-4. Epub 2013 Jun 20.
5
Long-acting β2-agonists increase fluticasone propionate-induced mitogen-activated protein kinase phosphatase 1 (MKP-1) in airway smooth muscle cells.长效β2-激动剂增加了气道平滑肌细胞中丙酸氟替卡松诱导的丝裂原活化蛋白激酶磷酸酶 1(MKP-1)。
PLoS One. 2013;8(3):e59635. doi: 10.1371/journal.pone.0059635. Epub 2013 Mar 22.
6
Corticosteroid resistance in patients with asthma and chronic obstructive pulmonary disease.哮喘和慢性阻塞性肺疾病患者的皮质类固醇抵抗。
J Allergy Clin Immunol. 2013 Mar;131(3):636-45. doi: 10.1016/j.jaci.2012.12.1564. Epub 2013 Jan 26.
7
Combination of a selective activator of the glucocorticoid receptor Compound A with a proteasome inhibitor as a novel strategy for chemotherapy of hematologic malignancies.选择性糖皮质激素受体激活剂化合物 A 与蛋白酶体抑制剂联合用于血液系统恶性肿瘤的化疗新策略。
Cell Cycle. 2013 Jan 1;12(1):133-44. doi: 10.4161/cc.23048. Epub 2012 Dec 19.
8
Sphingosine 1-phosphate induces MKP-1 expression via p38 MAPK- and CREB-mediated pathways in airway smooth muscle cells.鞘氨醇-1-磷酸通过p38丝裂原活化蛋白激酶和环磷腺苷效应元件结合蛋白介导的途径诱导气道平滑肌细胞中双特异性磷酸酶-1的表达。
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9
Cytokines alter glucocorticoid receptor phosphorylation in airway cells: role of phosphatases.细胞因子改变气道细胞中糖皮质激素受体的磷酸化:磷酸酶的作用。
Am J Respir Cell Mol Biol. 2012 Oct;47(4):464-73. doi: 10.1165/rcmb.2011-0364OC. Epub 2012 May 16.
10
Pathogenesis of severe asthma.严重哮喘的发病机制。
Clin Exp Allergy. 2012 May;42(5):625-37. doi: 10.1111/j.1365-2222.2012.03983.x.

植物衍生物化合物A对气道平滑肌细胞中皮质类固醇抗性趋化因子产生的影响。

Effect of the plant derivative Compound A on the production of corticosteroid-resistant chemokines in airway smooth muscle cells.

作者信息

Gavrila Adelina, Chachi Latifa, Tliba Omar, Brightling Christopher, Amrani Yassine

机构信息

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.

出版信息

Am J Respir Cell Mol Biol. 2015 Nov;53(5):728-37. doi: 10.1165/rcmb.2014-0477OC.

DOI:10.1165/rcmb.2014-0477OC
PMID:25897650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4742953/
Abstract

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.

摘要

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。