Role of protein kinase R in double-stranded RNA-induced expression of nitric oxide synthase in human astroglia

被引:46
作者
Auch, CJ
Saha, RN
Sheikh, FG
Liu, XJ
Jacobs, BL
Pahan, K
机构
[1] Univ Nebraska, Med Ctr, Dept Oral Biol, Lincoln, NE 68583 USA
[2] US FDA, Div Therapeut Prot, Bethesda, MD 20892 USA
[3] Arizona State Univ, Dept Microbiol, Tempe, AZ 85287 USA
关键词
double-stranded RNA; human astroglia; inducible nitric oxide synthase; nuclear factor-kappa B; CCAAT/enhancer-binding protein beta;
D O I
10.1016/S0014-5793(04)00302-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Environmental factor(s), such as viral infection, has been implicated as one of the triggering events leading to neuro-inflammation in multiple sclerosis. This study underlines the importance of double-stranded RNA (dsRNA), the active component of a viral infection, in inducing the expression of inducible nitric oxide synthase (iNOS) in human astroglia. DsRNA in the form of synthetic polyinosinic-polycytidylic acid (poly IC) induced expression of iNOS and iNOS promoter-driven luciferase activity through activation of nuclear factor (NF)-kappaB and CCAAT/enhancer-binding proteinbeta (C/EBPbeta). In addition, we show that inhibitors of protein kinase R attenuated iNOS by suppressing the activation of NF-kappaB but not C/EBPbeta. In contrast, knock down of p38 mitogen-activated protein kinase (MAPK) attenuated iNOS by suppressing the activation of C/EBPbeta but not NF-kappaB. This study delineates a novel role of dsRNA in inducing the expression of iNOS through dsRNA-activated protein kinase (PKR)-mediated activation of NF-kappaB and p38-mediated activation of C/EBPbeta in human astroglia that may participate in virus-induced neurological abnormalities. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:223 / 228
页数:6
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