Effects of Ubiquinol-10 on MicroRNA-146a Expression In Vitro and In Vivo

被引:28
作者
Schmelzer, Constance [1 ]
Kitano, Mitsuaki [3 ]
Rimbach, Gerald [2 ]
Niklowitz, Petra [4 ]
Menke, Thomas [4 ]
Hosoe, Kazunori [5 ]
Doering, Frank [1 ]
机构
[1] Univ Kiel, Inst Human Nutr & Food Sci, D-24118 Kiel, Germany
[2] Univ Kiel, Inst Human Nutr & Food Sci, D-24098 Kiel, Germany
[3] Kaneka Corp, Frontier Biochem & Med Res Labs, Takasago, Hyogo, Japan
[4] Univ Written Herdecke, Vest Kinder & Jugendklin Datteln, D-45711 Datteln, Germany
[5] Kaneka Corp, Funct Food Ingredients Div, Osaka, Japan
关键词
COENZYME Q(10); TNF-ALPHA; SUPPLEMENTATION; PLASMA; METABOLISM; ENRICHMENT; CHEMOKINES; SECRETION; DAMAGE; GENES;
D O I
10.1155/2009/415437
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
MicroRNAs (miRs) are involved in key biological processes via suppression of gene expression at posttranscriptional levels. According to their superior functions, subtle modulation of miR expression by certain compounds or nutrients is desirable under particular conditions. Bacterial lipopolysaccharide (LPS) induces a reactive oxygen species-/NF-kappa B-dependent pathway which increases the expression of the anti-inflammatory miR-146a. We hypothesized that this induction could be modulated by the antioxidant ubiquinol-10. Preincubation of human monocytic THP-1 cells with ubiquinol-10 reduced the LPS-induced expression level of miR-146a to 78.9 +/- 13.22%. In liver samples of mice injected with LPS, supplementation with ubiquinol-10 leads to a reduction of LPS-induced miR-146a expression to 78.12 +/- 21.25%. From these consistent in vitro and in vivo data, we conclude that ubiquinol-10 may fine-tune the inflammatory response via moderate reduction of miR-146a expression. Copyright (C) 2009 Constance Schmelzer et al.
引用
收藏
页数:7
相关论文
共 29 条
[1]   CoQ10 supplementation elevates the epidermal CoQ10 level in adult hairless mice [J].
Ashida, Yutaka ;
Yamanishi, Haruyo ;
Terada, Takatomo ;
Oota, Norihito ;
Sekine, Kyoichi ;
Watabe, Kazuo .
BIOFACTORS, 2005, 25 (1-4) :175-178
[2]   Relief of microRNA-mediated translational repression in human cells subjected to stress [J].
Bhattacharyya, Suvendra N. ;
Habermacher, Regula ;
Martine, Ursula ;
Closs, Ellen I. ;
Filipowicz, Witold .
CELL, 2006, 125 (06) :1111-1124
[3]   bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila [J].
Brennecke, J ;
Hipfner, DR ;
Stark, A ;
Russell, RB ;
Cohen, SM .
CELL, 2003, 113 (01) :25-36
[4]   The evolution of gene regulation by transcription factors and microRNAs [J].
Chen, Kevin ;
Rajewsky, Nikolaus .
NATURE REVIEWS GENETICS, 2007, 8 (02) :93-103
[5]   The role of microRNAs in sensing nutrient stress [J].
Chiou, Tzyy-Jen .
PLANT CELL AND ENVIRONMENT, 2007, 30 (03) :323-332
[6]   Principles of microRNA regulation of a human cellular signaling network [J].
Cui, Qinghua ;
Yu, Zhenbao ;
Purisima, Enrico O. ;
Wang, Edwin .
MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1)
[7]   Regulation of ubiquinone metabolism [J].
Dallner, G ;
Sindelar, PJ .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (3-4) :285-294
[8]   Functional connections and pathways of coenzyme Q10-inducible genes:: an In-silico study [J].
Doering, Frank ;
Schmelzer, Constance ;
Lindner, Inka ;
Vock, Christina ;
Fujii, Kenji .
IUBMB LIFE, 2007, 59 (10) :628-633
[9]   miR-122 regulation of lipid metabolism revealed by in vivo antisense targeting [J].
Esau, C ;
Davis, S ;
Murray, SF ;
Yu, XX ;
Pandey, SK ;
Pear, M ;
Watts, L ;
Booten, SL ;
Graham, M ;
McKay, R ;
Subramaniam, A ;
Propp, S ;
Lollo, BA ;
Freier, S ;
Bennett, CF ;
Bhanot, S ;
Monia, BP .
CELL METABOLISM, 2006, 3 (02) :87-98
[10]   Biological validation of coenzyme Q redox state by HPLC-EC measurement:: relationship between coenzyme Q redox state and coenzyme Q content in rat tissues [J].
Galinier, A ;
Carrière, A ;
Fernandez, Y ;
Bessac, AM ;
Caspar-Bauguil, S ;
Periquet, B ;
Comtat, M ;
Thouvenot, JP ;
Casteilla, L .
FEBS LETTERS, 2004, 578 (1-2) :53-57