AQP9 protein phosphorylation decreases arsenic influx in mammal cells / 中国药学杂志
Chinese Pharmaceutical Journal
; (24): 679-683, 2012.
Article
in Zh
| WPRIM
| ID: wpr-860739
Responsible library:
WPRO
ABSTRACT
OBJECTIVE: To detect the levels of aquaglyceroporin 9 (AQP9) mRNA expression, AQP9 and p38 proteins and their phosphorylation in HepG2 and L-02 cells treated with NaAsO2, and to investigate the association of these expression levels with arsenic intake and the AQP9 phosphorylation mechanism. METHODS: The intracellular arsenic content was determined by inductively coupled plasma mass spectrometry (ICP-MS). Real-time quantitative PCR, Western blotting and immunoprecipitation techniques were used to detect AQP9 mRNA, AQP9 and p38 protein levels and their phosphorylation levels in HepG2 and L-02 cells. SPSS statistical software was used to analyze experimental data. RESULTS: Intracellular arsenic content and intake rate in HepG2 cells were faster than those in L-02 cells. AQP9 mRNA levels in L-02 cells was increased with time within 6 h after NaAsO2 treatment (P<0.05), while no significant change was observed in L-02 cells. Two hours after treatment, AQP9 gene levels in HepG2 cells were all significantly increased at different concentrations of NaAs02. The phosphorylation levels of AQP9 in HepG2 cells were increased with treating time and concentration of NaAsO2. While the phosphorylation levels of AQP9 in L-02 cells significantly increased compared to control at each time point and concentration, but no significant difference was shown between the treatments. p38 phosphorylation levels in both cells were increased with time. Inhibition of p38 activity by SB203580 completely abolished AQP9 protein phosphorylation in L-02 cells, while it had no significant effect on HepG2 cells. CONCLUSION: AQP9 expression and phosphorylation levels may play an important role in regulating arsenic influx; regulation mechanism of AQP9 phosphorylation may be different in different cells. Copyright 2012 by the Chinese Pharmaceutical Association.
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WPRIM
Language:
Zh
Journal:
Chinese Pharmaceutical Journal
Year:
2012
Type:
Article