Divergent E1 and E2 epithelial differentiation and associated regulatory mechanisms of IL-20 family members
Divergent E1 and E2 epithelial differentiation and associated regulatory mechanisms of IL-20 family members
批准号:
398577603
负责人:
Professor Dr. Carsten B. Schmidt-Weber, Ph.D.
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2018
资助国家:
德国
项目状态:
已结题
起止时间:
2017-12-31 至 2021-12-31
中文摘要
过敏影响了20%的人口,并且呈上升趋势。致敏的原因,特别是机制尚不清楚。上皮细胞在这一过程中发挥着重要作用,因为它们不仅形成屏障,而且在抗原进入机体时有助于第一次上下文识别。到目前为止,还不知道上皮细胞是否会分化为促过敏E2型或可能对感染很重要的E2型。在T细胞和巨噬细胞中也观察到这种表型印迹。初步证据表明,这种分化也调节了免疫调节的上皮机制,特别是IL-20家族的机制。这组基因被怀疑与抗炎反应有关,可能与气道炎症后的康复有关。因此,探索上皮分化机制以及多能性上皮前体细胞是否受到影响是本研究的关键目标,因为这些与上皮表面的再生有关。事实上,初步数据表明E2启动发生在基底细胞水平,E2启动在尘螨致敏小鼠气管基底细胞中显著增加。这一水平的影响可能对受影响的患者产生持续影响。此外,该项目希望阐明不同的上皮表型是否会引起对细菌病原体的不同反应,细菌病原体通常在气道疾病(如哮喘)的恶化中起作用。IL-20家族的调控是该研究的重点,因为该介质被认为介导上皮恢复。由于新的治疗方法很容易接触到气道上皮,因此本研究可以为变应性气道疾病的治疗开辟新的选择。
英文摘要
Allergy affects 20% of the population with an increasing trend. The cause and in particular the mechanism of sensitization are yet unknown. Epithelial cells are playing an important role in this process as they are not only forming a barrier, but also contribute to the first context recognition when the antigen is entering the organism. So far, it was not known that epithelial cells undergo a differentiation that polarizes the cells either to a pro-allergic E2-type or an E2 type that is likely to be important for infections. This kind of phenotype imprinting was observed also for T cells or macrophages. Preliminary evidences suggest that this differentiation also modulates epithelial mechanisms of immune regulation, particularly those of the IL-20 family. This group of genes is suspected in anti-inflammatory responses and could be relevant for reconvalescense following airway inflammation. It is therefore a key objective of the research proposal to explore the epithelial differentiation mechanisms and also whether pluripotent epithelial precursor cells are affected, since these are relevant for the regeneration of the epithelial surface. In fact preliminary data suggest that E2 priming occurs on the basal cell level and that E2 priming is dramatically increased in basal cells of trachea of house dust mite sensitized mice. An impact on this level could have a sustained effect for affected patients. In addition the project wants to elucidate whether the distinct epithelial phenotypes give rise to differential responses to bacterial pathogens that are commonly playing a role in exacerbation of airways diseases such as asthma. The regulation of the IL-20 family is a focus of the study readouts as the mediators are thought to mediate epithelial recovery. Since the airway epithelium is well accessible for novel therapeutics, the proposed research can open novel therapeutic option for allergic airway diseases.
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