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TTF-1、Gata-6 和 FoxA2 对 claudin-6 的发育肺表达和转录调控。

Developmental lung expression and transcriptional regulation of claudin-6 by TTF-1, Gata-6, and FoxA2.

机构信息

Department of Physiology and Developmental Biology, Brigham Young University, 3054 Life Sciences Building, Provo, UT 84602, USA.

出版信息

Respir Res. 2014 Jun 26;15(1):70. doi: 10.1186/1465-9921-15-70.

Abstract

BACKGROUND

Claudins are transmembrane proteins expressed in tight junctions that prevent paracellular transport of extracellular fluid and a variety of other substances. However, the expression profile of Claudin-6 (Cldn6) in the developing lung has not been characterized.

METHODS AND RESULTS

Cldn6 expression was determined during important periods of lung organogenesis by microarray analysis, qPCR and immunofluorescence. Expression patterns were confirmed to peak at E12.5 and diminish as lung development progressed. Immunofluorescence revealed that Cldn6 was detected in cells that also express TTF-1 and FoxA2, two critical transcriptional regulators of pulmonary branching morphogenesis. Cldn6 was also observed in cells that express Sox2 and Sox9, factors that influence cell differentiation in the proximal and distal lung, respectively. In order to assess transcriptional control of Cldn6, 0.5, 1.0, and 2.0-kb of the proximal murine Cldn6 promoter was ligated into a luciferase reporter and co-transfected with expression vectors for TTF-1 or two of its important transcriptional co-regulators, FoxA2 and Gata-6. In almost every instance, TTF-1, FoxA2, and Gata-6 activated gene transcription in cell lines characteristic of proximal airway epithelium (Beas2B) and distal alveolar epithelium (A-549).

CONCLUSIONS

These data revealed for the first time that Cldn6 might be an important tight junctional component expressed by pulmonary epithelium during lung organogenesis. Furthermore, Cldn6-mediated aspects of cell differentiation may describe mechanisms of lung perturbation coincident with impaired cell junctions and abnormal membrane permeability.

摘要

背景

Claudin 是紧密连接中表达的跨膜蛋白,可防止细胞外液和多种其他物质的旁细胞转运。然而,Claudin-6(Cldn6)在发育中的肺中的表达谱尚未得到描述。

方法和结果

通过微阵列分析、qPCR 和免疫荧光,在肺器官发生的重要时期确定 Cldn6 的表达。表达模式被证实在 E12.5 时达到峰值,并随着肺发育的进行而减少。免疫荧光显示,Cldn6 存在于表达 TTF-1 和 FoxA2 的细胞中,这两种因子是肺分支形态发生的关键转录调节因子。Cldn6 也存在于表达 Sox2 和 Sox9 的细胞中,这两个因子分别影响近端和远端肺的细胞分化。为了评估 Cldn6 的转录控制,将 0.5、1.0 和 2.0-kb 的近端鼠 Cldn6 启动子与荧光素酶报告基因连接,并与 TTF-1 或其两个重要转录共调节剂 FoxA2 和 Gata-6 的表达载体共转染。在几乎所有情况下,TTF-1、FoxA2 和 Gata-6 都能激活具有近端气道上皮(Beas2B)和远端肺泡上皮(A-549)特征的细胞系中的基因转录。

结论

这些数据首次表明,Cldn6 可能是肺器官发生过程中肺上皮表达的重要紧密连接成分。此外,Cldn6 介导的细胞分化方面可能描述了与细胞连接受损和膜通透性异常相关的肺干扰机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac74/4082679/77e69d789154/1465-9921-15-70-1.jpg

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