Expression of Clu and Tgfb1 during murine tooth development: effects of in-vivo transfection with anti-miR-214

被引:28
作者
Khan, Qalb-E-Saleem [1 ]
Sehic, Amer [1 ]
Khuu, Cuong [1 ]
Risnes, Steinar [1 ]
Osmundsen, Harald [1 ]
机构
[1] Univ Oslo, Dept Oral Biol, N-0316 Oslo, Norway
关键词
clusterin; eruption; miR-214; mouse molar; transforming growth factor beta-1; GROWTH-FACTOR-BETA; MESSENGER-RNA; PRION PROTEIN; CLUSTERIN EXPRESSION; GENE-EXPRESSION; CELL-DEATH; LOCALIZATION; ERUPTION; DIFFERENTIATION; MECHANISMS;
D O I
10.1111/eos.12056
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Expression of clusterin (Clu) in the murine first molar tooth germ was markedly increased at postnatal developmental stages. The time-course of expression of this gene paralleled those of other genes encoding proteins involved during the secretory phase of odontogenesis, as described previously. Immunohistochemical studies of clusterin in murine molar tooth germs suggested this protein to be located in outer enamel epithelium, regressing enamel organ, secretory ameloblasts, and the dental epithelium connecting the tooth to the oral epithelium at an early eruptive stage. Immunolabelling of transforming growth factor beta-1 (TGF-1) revealed it to be located close to clusterin. The levels of expression of Clu and Tgfb1 were markedly decreased following in-vivo transfection with anti-miR-214. In contrast, the expression of several genes associated with regulation of growth and development were increased by this treatment. We suggest that clusterin has functions during secretory odontogenesis and the early eruptive phase. Bioinformatic analysis after treatment with anti-miR-214 suggested that, whilst cellular activities associated with tooth mineralization and eruption were inhibited, activities associated with an alternative developmental activity (i.e. biosynthesis of contractile proteins) appeared to be stimulated. These changes probably occur through regulation mediated by a common cluster of transcription factors and support suggestions that microRNAs (miRNAs) are highly significant as regulators of differentiation during odontogenesis.
引用
收藏
页码:303 / 312
页数:10
相关论文
共 56 条
[1]   Clusterin expression in cholestasis, hepatocellular carcinoma and liver fibrosis [J].
Aigelsreiter, Ariane ;
Janig, Elke ;
Sostaric, Julia ;
Pichler, Martin ;
Unterthor, Daniela ;
Halasz, Judith ;
Lackner, Carolin ;
Zatloukal, Kurt ;
Denk, Helmut .
HISTOPATHOLOGY, 2009, 54 (05) :561-570
[2]   Extending the loop design for two-channel microarray experiments [J].
Altman, Naomi S. ;
Hua, Jun .
GENETICAL RESEARCH, 2006, 88 (03) :153-163
[3]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[4]   MicroRNAs in Organogenesis and Disease [J].
Asli, Naisana S. ;
Pitulescu, Mara E. ;
Kessel, Michael .
CURRENT MOLECULAR MEDICINE, 2008, 8 (08) :698-710
[5]   Heat shock-initiated apoptosis is accelerated and removal of damaged cells is delayed in the testis of clusterin/Apoj knock-out mice [J].
Bailey, RW ;
Aronow, B ;
Harmony, JAK ;
Griswold, MD .
BIOLOGY OF REPRODUCTION, 2002, 66 (04) :1042-1053
[6]   H19 mRNA-like noncoding RNA promotes breast cancer cell proliferation through positive control by E2F1 [J].
Berteaux, N ;
Lottin, V ;
Monté, D ;
Pinte, S ;
Quatannens, B ;
Coll, J ;
Hondermarck, H ;
Curgy, JJ ;
Dugimont, T ;
Adriaenssens, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (33) :29625-29636
[7]   Loss of TGF-β1 leads to increased neuronal cell death and microgliosis in mouse brain [J].
Brionne, TC ;
Tesseur, I ;
Masliah, E ;
Wyss-Coray, T .
NEURON, 2003, 40 (06) :1133-1145
[8]  
CHINDIA ML, 1991, E AFR MED J, V68, P276
[9]   Rosmarinic acid ameliorates acute liver damage and fibrogenesis in carbon tetrachloride-intoxicated mice [J].
Domitrovic, Robert ;
Skoda, Marko ;
Marchesi, Vanja Vasiljev ;
Cvijanovic, Olga ;
Pugel, Ester Pernjak ;
Stefan, Maja Bival .
FOOD AND CHEMICAL TOXICOLOGY, 2013, 51 :370-378
[10]   TEMPORAL AND SPATIAL PATTERNS OF TRANSFORMING GROWTH FACTOR-BETA-1 EXPRESSION IN DEVELOPING RAT MOLARS [J].
DSOUZA, RN ;
HAPPONEN, RP ;
RITTER, NM ;
BUTLER, WT .
ARCHIVES OF ORAL BIOLOGY, 1990, 35 (12) :957-965