Role of miR-122 Targeting AldoA in The Metabolism of ob/ob Mice

被引:0
|
作者
Fang Zhi-Juan [1 ]
Li Peng [1 ]
Duo Wen-Li [1 ]
Jiang Ting [1 ]
Zhang Chen-Yu [1 ]
Xiang Yang [1 ]
机构
[1] Nanjing Univ, Sch Life Sci, State Key Lab Pharmaceut Biotechnol, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-122; ob/ob mice; AldoA; type; 2; diabete; MESSENGER-RNAS; MICRORNAS; EXPRESSION; EXOSOMES; PATHOPHYSIOLOGY; MICROVESICLES; BIOGENESIS; CANCER; SERUM;
D O I
10.3724/SP.J.1206.2013.00097
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
In previous study, our group have found that there is a significant increased level of miR-122 in the serum of ob/ob mice, an animal model of type 2 diabetes. Here, we further investigated the role of miR-122 targeting AldoA in the liver of ob/ob mice. First, a significant decrease of miR-122 level and a notable increase of AldoA expression was found in the liver of the ob/ob mice. Second, mature miR-122 was transfected into 293T cells and then MVs isolated from 293T cells were collected; qRT-PCR was applied to confirm that miR-122 was rich in MVs. Third, specific fluorescent dye DiI-C-18-labeled MVs were injected intravenously into BALB/c mice; the frozen section of liver was observed through fluorescent microscopy. Finally, miR-122 targeting AldoA in the metabolism of ob/ob mice was confirmed by qRT-PCR and Western blotting. AldoA mainly catalysed the transformation between dihydroxyacetone phosphate, glyceraldehyde-3- phosphate and fructose 1, 6 - bisphosphate in glycolytic pathway. MiR-122 may play an important role in the pathologenesis of ob/ob mice through AldoA pathway.
引用
收藏
页码:185 / 191
页数:7
相关论文
共 29 条
  • [1] The functions of animal microRNAs
    Ambros, V
    [J]. NATURE, 2004, 431 (7006) : 350 - 355
  • [2] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [3] Chang Jinhong, 2004, RNA Biol, V1, P106, DOI 10.4161/rna.1.2.1066
  • [4] Chen X, 2011, INT J CANCER, V130, P1002
  • [5] Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases
    Chen, Xi
    Ba, Yi
    Ma, Lijia
    Cai, Xing
    Yin, Yuan
    Wang, Kehui
    Guo, Jigang
    Zhang, Yujing
    Chen, Jiangning
    Guo, Xing
    Li, Qibin
    Li, Xiaoying
    Wang, Wenjing
    Zhang, Yan
    Wang, Jin
    Jiang, Xueyuan
    Xiang, Yang
    Xu, Chen
    Zheng, Pingping
    Zhang, Juanbin
    Li, Ruiqiang
    Zhang, Hongjie
    Shang, Xiaobin
    Gong, Ting
    Ning, Guang
    Wang, Jun
    Zen, Ke
    Zhang, Junfeng
    Zhang, Chen-Yu
    [J]. CELL RESEARCH, 2008, 18 (10) : 997 - 1006
  • [6] Shedding microvesicles: artefacts no more
    Cocucci, Emanuele
    Racchetti, Gabriella
    Meldolesi, Jacopo
    [J]. TRENDS IN CELL BIOLOGY, 2009, 19 (02) : 43 - 51
  • [7] Antagonism of microRNA-122 in mice by systemically administered LNA-antimiR leads to up-regulation of a large set of predicted target mRNAs in the liver
    Elmen, Joacim
    Lindow, Morten
    Silahtaroglu, Asli
    Bak, Mads
    Christensen, Mette
    Lind-Thomsen, Allan
    Hedtjarn, Maj
    Hansen, Jens Bo
    Hansen, Henrik Frydenlund
    Straarup, Ellen Marie
    McCullagh, Keith
    Kearney, Phil
    Kauppinen, Sakari
    [J]. NUCLEIC ACIDS RESEARCH, 2008, 36 (04) : 1153 - 1162
  • [8] The evolving diabetes burden in the United States
    Engelgau, MM
    Geiss, LS
    Saaddine, JB
    Boyle, JP
    Benjamin, SM
    Gregg, EW
    Tierney, EF
    Rios-Burrows, N
    Mokdad, AH
    Ford, ES
    Imperatore, G
    Narayan, KMV
    [J]. ANNALS OF INTERNAL MEDICINE, 2004, 140 (11) : 945 - 950
  • [9] miR-122 regulation of lipid metabolism revealed by in vivo antisense targeting
    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
    [J]. CELL METABOLISM, 2006, 3 (02) : 87 - 98
  • [10] miR-122 targeting with LNA/2′-O-methyl oligonucleotide mixmers, peptide nucleic acids (PNA), and PNA-peptide conjugates
    Fabani, Martin M.
    Gait, Michael J.
    [J]. RNA, 2008, 14 (02) : 336 - 346