No induction of anti-viral responses in human cell lines HeLa and MCF-7 when transfecting with siRNA or siLNA

被引:23
作者
Dahlgren, C
Wahlestedt, C
Thonberg, H
机构
[1] Karolinska Inst, Programme Genom & Bioinformat, Dept Cell & Microbiol, S-17177 Stockholm, Sweden
[2] Scripps Florida, Neurosci Discovery, Jupiter, FL 33458 USA
关键词
siRNA; siLNA; RNAi; off-target; interferon; RNA interference; cell cultures;
D O I
10.1016/j.bbrc.2006.01.085
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene silencing by RNAi and siRNAs has become a well-used tool for researchers. Because of its relatively small size, siRNA was originally thought to avoid activation of anti-viral responses. Recent reports demonstrating so-called "off-target effects" are therefore alarming. One issue raised is that siRNA induces interferon-regulated genes at the transcriptional level. We characterize the anti-viral responses of synthetic siRNA and in vitro-transcribed siRNA by measuring the mRNA. levels of IFN-beta and OAS2 in HeLa cells. Transfections with both traditional and LNA-modified synthetic siRNA cause no anti-viral responses, whereas transfection with either long dsRNA or in vitro-transcribed siRNA leads to greater than 1000-fold induction of these genes. The lack of response was also demonstrated at the level of phosphorylated eIF2 alpha, and measuring of IFN-beta by ELISA in cell culture media from the human cell line MCF-7. Altogether, transfection with synthetic siRNA does not induce anti-viral responses in these two cell lines. Our results reinforce the role of siRNA as an effective tool for reverse genetics and strengthen siLNA as a tool for future therapeutic applications. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1211 / 1217
页数:7
相关论文
共 31 条
[1]   Lentiviral-mediated RNA interference [J].
Abbas-Terki, T ;
Blanco-Bose, W ;
Déglon, N ;
Pralong, W ;
Aebischer, P .
HUMAN GENE THERAPY, 2002, 13 (18) :2197-2201
[2]   RNA-dependent RNA polymerases, viruses, and RNA silencing [J].
Ahlquist, P .
SCIENCE, 2002, 296 (5571) :1270-1273
[3]   RNAi-induced gene silencing by local electroporation in targeting brain region [J].
Akaneya, Y ;
Jiang, B ;
Tsumoto, T .
JOURNAL OF NEUROPHYSIOLOGY, 2005, 93 (01) :594-602
[4]   Inhibition of respiratory viruses by nasally administered siRNA [J].
Bitko, V ;
Musiyenko, A ;
Shulyayeva, O ;
Barik, S .
NATURE MEDICINE, 2005, 11 (01) :50-55
[5]  
BOMMER UA, 1981, ACTA BIOL MED GER, V40, P1105
[6]   RNA interference in mammalian cells by chemically-modified RNA [J].
Braasch, DA ;
Jensen, S ;
Liu, YH ;
Kaur, K ;
Arar, K ;
White, MA ;
Corey, DR .
BIOCHEMISTRY, 2003, 42 (26) :7967-7975
[7]   Induction of an interferon response by RNAi vectors in mammalian cells [J].
Bridge, AJ ;
Pebernard, S ;
Ducraux, A ;
Nicoulaz, AL ;
Iggo, R .
NATURE GENETICS, 2003, 34 (03) :263-264
[8]   Apoptosis and interferons: Role of interferon-stimulated genes as mediators of apoptosis [J].
Chawla-Sarkar, M ;
Lindner, DJ ;
Liu, YF ;
Williams, B ;
Sen, GC ;
Silverman, RH ;
Borden, EC .
APOPTOSIS, 2003, 8 (03) :237-249
[9]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[10]   Locked nucleic acid (LNA) mediated improvements in siRNA stability and functionality [J].
Elmén, J ;
Thonberg, H ;
Ljungberg, K ;
Frieden, M ;
Westergaard, M ;
Xu, YH ;
Wahren, B ;
Liang, ZC ;
Urum, H ;
Koch, T ;
Wahlestedt, C .
NUCLEIC ACIDS RESEARCH, 2005, 33 (01) :439-447