Smoking-Induced Expression of the GPR15 Gene Indicates Its Potential Role in Chronic Inflammatory Pathologies

被引:63
作者
Koks, Gea [1 ]
Uudelepp, Mari-Liis [1 ,2 ]
Limbach, Maia [1 ]
Peterson, Peart [1 ]
Reimann, Ene [1 ,3 ]
Koks, Sulev [1 ,3 ]
机构
[1] Univ Tartu, Inst Biomed & Translat Med, EE-50411 Tartu, Estonia
[2] Tartu Univ Hosp, Dept Genet, Tartu, Estonia
[3] Estonian Univ Life Sci, Dept Reprod Biol, Tartu, Estonia
关键词
DIFFERENTIAL DNA METHYLATION; BLOOD MONONUCLEAR-CELLS; RECEPTOR GPR15; TOBACCO-SMOKING; CROHNS-DISEASE; BOWEL-DISEASE; UNITED-STATES; LIFE-STYLE; PSORIASIS; HYPOMETHYATION;
D O I
10.1016/j.ajpath.2015.07.006
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Despite the described clear epigenetic effects of smoking, the effect of smoking on genome-wide gene expression in the blood is obscure. We therefore studied the smoking-induced changes in the gene-expression profile of the peripheral blood. RNA was extracted from the whole blood of 48 individuals with a detailed smoking history (24 never-smokers, 16 smokers, and 8 ex-smokers). Gene-expression profiles were evaluated with RNA sequencing, and results were analyzed separately in 24 men and 24 women. In the male smokers, 13 genes were statistically significantly (false-discovery rate <0.1) differentially expressed; in female smokers, 5 genes. Although most of the differentially expressed genes were different between the male and female smokers, the G-protein coupled receptor 15 gene (GPR15) was differentially expressed in both male and female smokers compared with never-smokers. Analysis of GPR15 methylation identified significantly greater hypomethylation in smokers compared with that in never-smokers. GPR15 is the chemoattractant receptor that regulates T-cell migration and immunity. Up-regulation of GPR15 could explain to some extent the health hazards of smoking with regard to chronic inflammatory diseases.
引用
收藏
页码:2898 / 2906
页数:9
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