The tyrosine phosphatase, SHP-1, is involved in bronchial mucin production during oxidative stress
| Autor: | Zhou Zhu, Yun Jeong Bae, Min Kyoung Jang, Hee Bom Moon, Sae Hoon Kim, You Sook Cho, Tae-Bum Kim, Keun Ae Moon, Chan Sun Park, Ki-Young Lee |
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| Rok vydání: | 2010 |
| Předmět: |
MAPK/ERK pathway
p38 mitogen-activated protein kinases Biophysics Bronchi Mice Inbred Strains Protein tyrosine phosphatase Biology Mucin 5AC medicine.disease_cause Biochemistry p38 Mitogen-Activated Protein Kinases Mice Cell Line Tumor medicine Animals Humans Molecular Biology Gene knockdown Protein Tyrosine Phosphatase Non-Receptor Type 6 Mucin Cell Biology Hydrogen Peroxide respiratory system Mucus Molecular biology Oxidative Stress Gene Expression Regulation Gene Knockdown Techniques Oxidative stress Proto-oncogene tyrosine-protein kinase Src |
| Zdroj: | Biochemical and biophysical research communications. 393(1) |
| ISSN: | 1090-2104 |
| Popis: | Mucus hypersecretion is a clinically important manifestation of chronic inflammatory airway diseases, such as asthma and Chronic obstructive pulmonary disease (COPD). Mucin production in airway epithelia is increased under conditions of oxidative stress. Src homology 2 domain-containing protein tyrosine phosphatase (SHP)-1 suppression is related to the development of airway inflammation and increased ROS levels. In this study, we investigated the role of SHP-1 in mucin secretion triggered by oxidative stress. Human lung mucoepidermoid H292 carcinoma cells were transfected with specific siRNA to eliminate SHP-1 gene expression. Cultured cells were treated with hydrogen peroxide (H(2)O(2)), and Mucin 5AC(MUC5AC) gene expression and mucin production were determined. Activation of p38 mitogen activated protein kinase (MAPK) in association with MUC5AC production was evaluated. N-acetylcysteine (NAC) was employed to determine whether antioxidants could block MUC5AC production. To establish the precise role of p38, mucin expression was observed after pre-treatment of SHP-1-depleted H292 cells with the p38 chemical blocker. We investigated the in vivo effects of oxidative stress on airway mucus production in SHP-1-deficient heterozygous (mev/+) mice. MUC5AC expression was enhanced in SHP-1 knockdown H292 cells exposed to H(2)O(2), compared to that in control cells. The ratio between phosphorylated and total p38 was significantly increased in SHP-1-deficient cells under oxidative stress. Pre-treatment with NAC suppressed both MUC5AC production and p38 activation. Blockage of p38 MAPK led to suppression of MUC5AC mRNA expression. Notably, mucin production was enhanced in the airway epithelia of mev/+ mice exposed to oxidative stress. Our results clearly indicate that SHP-1 plays an important role in airway mucin production through regulating oxidative stress. |
| Databáze: | OpenAIRE |
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