Nitric oxide and peroxynitrite induce gene expression of interleukin receptors increasing IL-21, IL-7, IL-1 and oncostatin M in cardiomyocytes

被引:4
|
作者
Rabkin, Simon W. [1 ]
机构
[1] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
关键词
Nitric oxide; Peroxynitrite; IL-1; R; IL-2; IL-21-R; IL-9 R oncostatin M; ACTIVATED PROTEIN-KINASE; MESSENGER-RNA EXPRESSION; ADULT CARDIAC MYOCYTES; TUMOR-NECROSIS-FACTOR; HUMAN T-CELLS; GAMMA-CHAIN; AUTOIMMUNE-DISEASE; ENDOTHELIAL-CELLS; HYDROGEN-PEROXIDE; DOWN-REGULATION;
D O I
10.1016/j.lfs.2009.11.002
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Aim: The objective of this investigation was to determine whether nitric oxide (NO) and peroxynitrite alter the gene expression of interleukin receptors (IL-R) in cardiomyocytes. Main methods: Cardiomyocytes, from neonatal mouse heart, in culture were treated with the NO donor 3-morpholinosydnonimine hydrochloride (SIN-1), which releases NO and peroxynitrite. IL-R gene expression was assessed by microarray analysis. Key findings: Gene expression data show that the IL-2 receptor family showed a highly significant and 1.7-fold increase in the gamma chain component which is common to all members of the IL-2 family receptors. There was a significant and 2-fold increase in IL-21 R and an increase of 1.8-fold in IL-7 R alpha gene expression. In contrast there was a significant 0.7-fold decrease in IL-9 R alpha. The IL-1 receptor family showed a significant and 1.4-fold increase in IL-1 RI compared to control but no change in IL-18 RI gene expression which was similar to control. The IL-6 family showed a significant increase in oncostatin M receptor gene expression of 1.3-fold but no change in IL-6 R alpha or IL-11 R alpha. Significance: These data suggest that NO/peroxynitrite by increasing gene expression of certain IL-Rs may magnify the effects of specific interleukins in conditions of excess interleukin production. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:45 / 51
页数:7
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