Airway Disease Section, NHLI Imperial College, London, United Kingdom.
Am J Respir Crit Care Med. 2010 Oct 1;182(7):897-904. doi: 10.1164/rccm.200906-0937OC. Epub 2010 Mar 11.
Patients with chronic obstructive pulmonary disease (COPD) show a poor response to corticosteroids. This has been linked to a reduction of histone deacetylase-2 as a result of oxidative stress and is reversed by theophylline.
To determine the role of phosphoinositide-3-kinase-delta (PI3K-δ) on the development of corticosteroid insensitivity in COPD and under oxidative stress, and as a target for theophylline.
Corticosteroid sensitivity was determined as the 50% inhibitory concentration of dexamethasone on tumor necrosis factor-α-induced interleukin-8 release in peripheral blood mononuclear cells from patients with COPD (n = 17) and compared with that of nonsmoking (n = 8) and smoking (n = 7) control subjects. The effect of theophylline and a selective PI3K-δ inhibitor (IC87114) on restoration of corticosteroid sensitivity was confirmed in cigarette smoke-exposed mice.
Peripheral blood mononuclear cells of COPD (50% inhibitory concentration of dexamethasone: 156.8 ± 32.6 nM) were less corticosteroid sensitive than those of nonsmoking (41.2 ± 10.5 nM; P = 0.018) and smoking control subjects (47.5 ± 19.6 nM; P = 0.031). Corticosteroid insensitivity and reduced histone deacetylase-2 activity after oxidative stress were reversed by a non-selective PI3K inhibitor (LY294002) and low concentrations of theophylline. Theophylline was a potent selective inhibitor of oxidant-activated PI3K-δ, which was up-regulated in peripheral lung tissue of patients with COPD. Furthermore, cells with knock-down of PI3K-δ failed to develop corticosteroid insensitivity with oxidative stress. Both theophylline and IC87114, combined with dexamethasone, inhibited corticosteroid-insensitive lung inflammation in cigarette-smoke-exposed mice in vivo.
Inhibition of oxidative stress dependent PI3K-δ activation by a selective inhibitor or theophylline provides a novel approach to reversing corticosteroid insensitivity in COPD.
慢性阻塞性肺疾病(COPD)患者对皮质类固醇的反应较差。这与氧化应激导致的组蛋白去乙酰化酶-2 减少有关,而茶碱可逆转这种情况。
确定磷酸肌醇-3-激酶-δ(PI3K-δ)在 COPD 患者和氧化应激下皮质类固醇不敏感的发展中的作用,以及作为茶碱的作用靶点。
通过测定肿瘤坏死因子-α诱导的白细胞介素-8 释放在 COPD 患者外周血单个核细胞中的 50%抑制浓度(IC50),来确定皮质类固醇的敏感性,然后与不吸烟(n=8)和吸烟(n=7)的对照组进行比较。在香烟烟雾暴露的小鼠中,通过测定茶碱和选择性 PI3K-δ 抑制剂(IC87114)对恢复皮质类固醇敏感性的影响,来证实这一作用。
COPD 患者的外周血单个核细胞(地塞米松的 50%抑制浓度:156.8±32.6 nM)比不吸烟(41.2±10.5 nM;P=0.018)和吸烟对照组(47.5±19.6 nM;P=0.031)的皮质类固醇敏感性更低。非选择性 PI3K 抑制剂(LY294002)和低浓度茶碱可逆转氧化应激后的皮质类固醇不敏感性和组蛋白去乙酰化酶-2 活性降低。茶碱是一种有效的氧化应激激活的 PI3K-δ 选择性抑制剂,在 COPD 患者的肺组织中上调。此外,敲低 PI3K-δ 的细胞在氧化应激下无法产生皮质类固醇不敏感。茶碱和 IC87114 与地塞米松联合使用,可抑制香烟烟雾暴露的小鼠体内皮质类固醇不敏感的肺部炎症。
通过选择性抑制剂或茶碱抑制依赖氧化应激的 PI3K-δ 激活,为逆转 COPD 中的皮质类固醇不敏感提供了一种新方法。