首页> 外文期刊>The Journal of Allergy and Clinical Immunology >Disease-specific expression and regulation of CCAAT/enhancer-binding proteins in asthma and chronic obstructive pulmonary disease.
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Disease-specific expression and regulation of CCAAT/enhancer-binding proteins in asthma and chronic obstructive pulmonary disease.

机译:哮喘和慢性阻塞性肺疾病中CCAAT /增强子结合蛋白的疾病特异性表达和调控。

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BACKGROUND: CCAAT/enhancer-binding proteins (C/EBPs) control cell proliferation; lack of C/EBPalpha correlates with increased proliferation of bronchial smooth muscle cells (BSMCs) of asthmatic patients. OBJECTIVE: We sought to assess disease-specific expression of C/EBPalpha, beta, delta, and epsilon and the effects of budesonide (10(-8) mol/L) and formoterol (10(-8) mol/L). METHODS: Expression and function of C/EBPalpha, beta, delta, and epsilon BSMCs of control subjects (n = 9), asthmatic patients (n = 12), and patients with chronic obstructive pulmonary disease (COPD; n = 10) were determined. RESULTS: The control group expressed C/EBPalpha, beta, delta, and epsilon, which were upregulated by serum (5%). Budesonide completely inhibited C/EBPalpha and beta expression; formoterol increased C/EBPalpha expression (2-fold). C/EBPdelta and epsilon expression were not affected by the drugs. The asthmatic group did not appropriately express C/EBPalpha. Basal levels of C/EBPbeta, delta, and epsilon were upregulated by serum (5%). Budesonide and formoterol increased C/EBPbeta levels (3.4-fold and 2.5-fold, respectively), leaving C/EBPalpha, delta, and epsilon levels unaffected. The COPD group normally expressed C/EBPalpha, beta, and epsilon, which were upregulated by serum treatment (5%). Basal levels of C/EBPdelta were downregulated by serum in 7 of 10 BSMC lines. Budesonide inhibited C/EBPalpha and beta expression, upregulated C/EBPdelta (3.2-fold), and had no effect on C/EBPepsilon. Formoterol upregulated C/EBPalpha expression (3-fold) but not the other C/EBPs. Protein analysis and electrophoretic mobility shift assay confirmed the disease-specific expression pattern of C/EBPalpha in asthmatic patients and C/EBPdelta in patients with COPD. CONCLUSIONS: The expression and regulation of C/EBPs in BSMCs of asthmatic patients and patients with COPD seems disease specific. Budesonide and formoterol modulate C/EBP expression in a drug- and disease-specific pattern. CLINICAL IMPLICATIONS: The data could provide amethod to discriminate between asthma and COPD at an early disease stage.
机译:背景:CCAAT /增强子结合蛋白(C / EBPs)控制细胞增殖。 C / EBPalpha的缺乏与哮喘患者的支气管平滑肌细胞(BSMC)增殖增加有关。目的:我们试图评估C / EBPalpha,β,δ和ε的疾病​​特异性表达以及布地奈德(10(-8)mol / L)和福莫特罗(10(-8)mol / L)的作用。方法:确定对照组(n = 9),哮喘患者(n = 12)和慢性阻塞性肺疾病(COPD; n = 10)患者的C / EBPalpha,β,δ和εBSMC的表达和功能。 。结果:对照组表达了C /EBPα,β,δ和ε,它们被血清(5%)上调。布地奈德完全抑制C / EBPalpha和beta表达;福莫特罗增加了C / EBPalpha表达(2倍)。 C / EBPdelta和ε表达不受药物影响。哮喘组未适当表达C / EBPalpha。血清(5%)上调了C / EBPbeta,δ和ε的基础水平。布地奈德和福莫特罗提高了C / EBPbeta水平(分别为3.4倍和2.5倍),而C / EBPalpha,δ和ε水平未受影响。 COPD组通常表达C / EBPalpha,β和epsilon,这些均通过血清治疗上调(5%)。在10个BSMC系中有7个的血清C / EBPdelta基础水平下调。布地奈德抑制C / EBPalpha和beta表达,上调C / EBPdelta(3.2倍),并且对C / EBPepsilon没有影响。福莫特罗上调C / EBPalpha表达(3倍),但不上调其他C / EBP。蛋白质分析和电泳迁移率变动分析证实了哮喘患者中C / EBPalpha的疾病特异性表达模式和COPD患者中C / EBPdelta的疾病特异性表达模式。结论:C / EBP在哮喘患者和COPD患者的BSMC中的表达和调节似乎是疾病特异性的。布地奈德和福莫特罗以药物和疾病特异性模式调节C / EBP表达。临床意义:数据可以提供一种在疾病早期区分哮喘和COPD的方法。

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