Cigarette smoke extract regulating the expression of γ-glutamylcysteine synthetase through the pathway of PI3K/Akt-Nrf2 in the bronchial epithelial cells of rats
10.3760/cma.j.issn.1008-1372.2010.01.003
- VernacularTitle:PI3K/Akt-Nrf2信号通路调节大鼠气道上皮细胞γ-谷氨酰半胱氨酸合成酶表达的研究
- Author:
Gang JIANG
;
Aiguo DAI
;
Ruicheng HU
- Publication Type:Journal Article
- Keywords:
1-phosphatidylinositol 3-kinase/ME;
DNA-Binding proteins/ME;
Glutamate-cysteine ligase/ME;
Smog/AE;
Signal transduction
- From:
Journal of Chinese Physician
2010;12(1):9-13
- CountryChina
- Language:Chinese
-
Abstract:
Objective To observe the effect of PDK ( phosphoinositol -3-kinase, PI3K)/Akt-Nrf2 (Nuclear factor -E2 related factor) signal pathway on γ-glutamylcysteine synthetase (γ-GCS) in the bronchial epithelial cells of rats treated with cigarette smoke extract (CSE). Methods The bronchial epithelial cells were dealt with 10% concentration of CSE for different time and pretreated with PI3k inhibitor (LY294002). The expressions of Nrf2,p-Akt and γ-GCS proteins were examined by immunocytochemistry, flow cytometry, immunofluorescence and western blot. The expressions of γ-GCS mRNA were detected by reverse transcription-polymerase chain reaction (RT-PCR). Reduced glutathione(GSH) content and the lev-el of γ-CCS activi-ty were examined. Results GSH content in CSElh group was significantly decreased, but still higher in CSE3 and 6 groups compared to the control. Nrf2 protein mainly located in the cytoplasm. Nrf2 plasmosin mainly increased in the nucleus in control group, and Nrf2 nucleic protein significantly enhanced in CSE1, 3 and 6 groups. P-Akt protein was up-regulated at lh, reached its peak at 3h, declined slightly at 6h after exposure to CSE. The tendency of the percentage of p-Akt positive cells was as same as p-Akt protein. γ-GCS mRNA, protein and activity, gradually increased in CSE lh, CSE 3h,CSE 6h groups. Pretreated with LY294002, the expression of p-Akt protein was markedly decreases, while Nrf2 plasmosin expressed strongly, and γ-GCS mRNA, protein, activity and GSH content were significantly decreased compared to CSE3h group. Linear correlation analysis demonstrated that there were a positive correlation among Nrf2 and γ-GCS,γ-GCS activity, and among p-Akt and Nrf2,GSH,γ-GCS,γ-GCS activity. Conclusion P13K/Akt signal path might participate in Nrf2 nuclear translocation via regulating the expression of γ-GCS.