Peripheral blood IRF1 expression as a marker for glucocorticoid sensitivity

被引:10
|
作者
Chapin, William J. [1 ]
Lenkala, Divya [2 ]
Mai, Yifeng [3 ]
Mao, Yushan [3 ]
White, Steven R. [2 ]
Huang, Rong S. [2 ,3 ]
机构
[1] Univ Chicago, Pritzker Sch Med, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[3] Ningbo Univ, Affiliated Hosp, Ningbo 315211, Zhejiang, Peoples R China
来源
PHARMACOGENETICS AND GENOMICS | 2015年 / 25卷 / 03期
关键词
airway; blood; gene expression; glucocorticoid; REGULATORY FACTOR-1 POLYMORPHISMS; OBSTRUCTIVE PULMONARY-DISEASE; NF-KAPPA-B; EPITHELIAL-CELLS; CORTICOSTEROID RESISTANCE; GENE-EXPRESSION; STEROID RESISTANCE; ASTHMATIC-PATIENTS; IFN-GAMMA; ASSOCIATION;
D O I
10.1097/FPC.0000000000000116
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objective Despite of the common usage of glucocorticoids (GCs), a significant portion of asthma patients exhibit GC insensitivity. This could be mediated by diverse mechanisms, including genomics. Recent work has suggested that measuring changes in gene expression may provide more predictive information about GC insensitivity than baseline gene expression alone, and that expression changes in peripheral blood may be reflective of those in the airway. Methods We performed in silico discovery using gene expression omnibus (GEO) data that evaluated GC effect on gene expression in multiple tissue types. Subsequently, candidate genes whose expression levels are affected by GC were examined in cell lines and in primary cells derived from human airway and blood. Results Through gene expression omnibus analysis, we identified interferon regulator factor 1 (IRF1), whose expression is affected by GC treatment in airway smooth muscle cells, normal human bronchial epithelial (NHBE) cells, and lymphoblastoid cell lines (LCLs). Significant IRF1 downregulation post GC exposure was confirmed in two cultured airway epithelial cell lines and primary NHBE cells (P<0.05). We observed large interindividual variation in GC-induced IRF1 expression changes among primary NHBE cells tested. Significant downregulation of IRF1 was also observed in six randomly selected LCLs (P<0.05), with variable degrees of downregulation among different samples. In peripheral blood mononuclear cells obtained from healthy volunteers, variable downregulation of IRF1 by GC was also shown. NFKB1, a gene whose expression is known to be downregulated by GC and the degree of downregulation of which is reflective of GC response, was used as a control in our study. IRF1 shows more consistent downregulation across tissue types when compared with NFKB1. Conclusion Our results suggest that GC-induced IRF1 gene expression changes in peripheral blood could be used as a marker to reflect GC response in the airway. Copyright (C) 2015 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:126 / 133
页数:8
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