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SPDEF regulates goblet cell hyperplasia in the airway epithelium

机译:SPDEF调节气道上皮中的杯状细胞增生

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摘要

Goblet cell hyperplasia and mucous hypersecretion contribute to the pathogenesis of chronic pulmonary diseases including cystic fibrosis, asthma, and chronic obstructive pulmonary disease. In the present work, mouse SAM pointed domain-containing ETS transcription factor (SPDEF) mRNA and protein were detected in subsets of epithelial cells lining the trachea, bronchi, and tracheal glands. SPDEF interacted with the C-terminal domain of thyroid transcription factor 1, activating transcription of genes expressed selectively in airway epithelial cells, including Sftpa, Scgb1a1, Foxj1, and Sox17. Expression of Spdef in the respiratory epithelium of adult transgenic mice caused goblet cell hyperplasia, inducing both acidic and neutral mucins in vivo, and stainined for both acidic and neutral mucins in vivo. SPDEF expression was increased at sites of goblet cell hyperplasia caused by IL-13 and dust mite allergen in a process that was dependent upon STAT-6. SPDEF was induced following intratracheal allergen exposure and after Th2 cytokine stimulation and was sufficient to cause goblet cell differentiation of Clara cells in vivo.
机译:杯状细胞增生和粘液过度分泌促成慢性肺部疾病的发病机理,包括囊性纤维化,哮喘和慢性阻塞性肺部疾病。在本工作中,在气管,支气管和气管内衬的上皮细胞亚群中检测到了小鼠SAM尖域含ETS转录因子(SPDEF)mRNA和蛋白质。 SPDEF与甲状腺转录因子1的C末端域相互作用,激活气道上皮细胞(包括Sftpa,Scgb1a1,Foxj1和Sox17)中选择性表达的基因的转录。 Spdef在成年转基因小鼠的呼吸道上皮中的表达引起杯状细胞增生,在体内诱导酸性和中性粘蛋白,并在体内对酸性和中性粘蛋白染色。在由STAT-6决定的过程中,由IL-13和尘螨过敏原引起的杯状细胞增生部位SPDEF表达增加。 SPDEF是在气管内变应原暴露后和Th2细胞因子刺激后诱导的,足以在体内引起Clara细胞的杯状细胞分化。

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