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Fibroblast growth factor 2-induced cytoplasmic asparaginyl-tRNA synthetase promotes survival of osteoblasts by regulating anti-apoptotic PI3K/Akt signaling.

 Su Jin Park  ;  Seong Hwan Kim  ;  Han Seok Choi  ;  Yumie Rhee  ;  Sung-Kil Lim 
 BONE, Vol.45(5) : 994-1003, 2009 
Journal Title
Issue Date
Animals ; Apoptosis/drug effects* ; Aspartate-tRNA Ligase/biosynthesis* ; Aspartate-tRNA Ligase/genetics ; Cell Proliferation/drug effects ; Cell Survival/drug effects ; Cells, Cultured ; Cytoplasm/drug effects ; Cytoplasm/enzymology ; Electrophoresis, Gel, Two-Dimensional ; Enzyme Induction/drug effects ; Fibroblast Growth Factor 2/pharmacology* ; Gene Expression Regulation, Enzymologic/drug effects ; Humans ; Mice ; Osteoblasts/cytology* ; Osteoblasts/drug effects ; Osteoblasts/enzymology* ; Phosphatidylinositol 3-Kinases/metabolism* ; Protein Kinase Inhibitors/pharmacology ; Proto-Oncogene Proteins c-akt/metabolism* ; RNA, Messenger/genetics ; RNA, Messenger/metabolism ; RNA, Small Interfering/metabolism ; RNA, Transfer, Amino Acyl/biosynthesis* ; RNA, Transfer, Amino Acyl/genetics ; Signal Transduction/drug effects ; Skull/cytology ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
FGF2 ; NARS ; Osteoblasts ; Survival ; PI3K/Akt pathway
Fibroblast growth factor 2 (FGF2), the potent bone anabolic agent, regulates the bone development, as well as the growth, remodeling and healing of the fracture. The intracellular signaling of FGF2 leads to activation of genes involved in cell proliferation, migration, differentiation and survival. However, little is known about FGF2-regulated proteins in the osteoblasts. Therefore, in this study, protein profiling in FGF2-treated MC3T3-E1 preosteoblast cells was evaluated using proteomic technologies. Six proteins including asparaginyl-tRNA synthetase (NARS), eukaryotic translation termination factor 1 (ETF1), GDP-forming succinyl-CoA synthetase (SUCLG2), heat shock protein 84 (HSP 84), sorting nexin 9 (SNX9) and alpha glucosidase 2alpha neutral subunit (GANAB) were increased more than 3-fold after the FGF2 treatment. Also, two proteins including beta-tropomyosin and tropomyosin 2 were decreased to 2-folds. Among these proteins, asparaginyl-tRNA synthetase (NARS), a member of aminoacyl-tRNA synthetases (AARS), was strikingly up-regulated more than 900-fold. The overexpression of NARS significantly increased the proliferation of both the MC3T3-E1 and the primary mouse calvarial cells. In contrast, significant reduction of the basal expression of NARS by siNARS remarkably suppressed the proliferation and induced the death of cell. After the siNARS treatment, the resistance to apoptosis induced by serum deprivation was also significantly reduced. The level of p-Akt was also reduced and the activity of caspase 3 significantly enhanced. In addition, NARS-induced protection against apoptosis was abolished by the treatment of PI3K inhibitors, wortmannin and LY294002. In conclusion, we suggest that NARS is one of the important mediators of FGF2 induced survival signaling in osteoblasts through the activation of PI3K/Akt survival pathway.
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1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Park, Su Jin(박수진)
Rhee, Yumie(이유미) ORCID logo https://orcid.org/0000-0003-4227-5638
Lim, Sung Kil(임승길)
Choi, Han Seok(최한석)
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