Cellular immunology · 2017
TSLP signaling blocking alleviates E-cadherin dysfunction of airway epithelium in a HDM-induced asthma model.
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Hu Yahui, Dong Hangming, Zou Mengchen, Huang Chaowen, Luo Lishan, Yu Changhui, Chen JiaLong, Xie Zhefan, Zhao Haijin, Le Yanqing, Zou Fei, Liu Laiyu, Cai Shaoxi
Аннотация
Recent studies have indicated that Thymic stromal lymphopoietin (TSLP) plays an important role in the prevention and treatment of asthma. However the role of TSLP in dysfunction of airway epithelial adherens junctions E-cadherin in house dust mite (HDM)-induced asthma has not been addressed. We hypothesized that TSLP contributed to HDM-induced E-cadherin dysfunction in asthmatic BALB/c mice and 16HBE cells. In vivo, a HDM-induced asthma mouse model was set up for 8weeks. Mice inhaled an anti-TSLP monoclonal antibody (mAb) before HDM. The mice treated with the anti-TSLP mAb ameliorated airway inflammation, the decreasing and aberrant distribution of E-cadherin and β-catenin as well as phosphorylation(p)-AKT induced by HDM. In vitro, HDM increased the expression of TSLP and E-cadherin dysfunction by PI3K/Akt signaling pathway. The exposure of 16HBE to TSLP resulted in redistribution of E-cadherin. These results indicate that TSLP may be an important contributor in E-cadherin dysfunction of HDM-induced asthma. TSLP signaling blocking shows a protective effect in mice and that the PI3K/Akt pathway may play a role in this process.
Предметные рубрики MeSH
Administration, InhalationAnimalsAntibodies, MonoclonalAsthmaBronchiBronchial HyperreactivityCadherinsCell LineChromonesCytokinesDisease Models, AnimalEpithelial CellsHumansLungMiceMice, Inbred BALB CMorpholinesOncogene Protein v-aktPhosphatidylinositol 3-KinasesPhosphorylationProtein Processing, Post-TranslationalPyroglyphidaeRandom AllocationSignal TransductionSpecific Pathogen-Free Organismsbeta CateninThymic Stromal Lymphopoietin