Wagner Christina, Isermann Kerstin, Fehrenbach Heinz, Roeder Thomas
Forschungszentrum Borstel, Department of Immunology and Cell Biology, Borstel, Germany.
BMC Genomics. 2008 Sep 29;9:446. doi: 10.1186/1471-2164-9-446.
Airway epithelial cells not only constitute a physical barrier, but also the first line of defence against airborne pathogens. At the same time, they are constantly exposed to reactive oxygen species. Therefore, airway epithelia cells have to possess a sophisticated innate immune system and a molecular armamentarium to detoxify reactive oxygen species. It has become apparent that deregulation of epithelial innate immunity is a major reason for the development of chronic inflammatory lung diseases. To elucidate the molecular architecture of the innate immune system of airway epithelial cells, we choose the fruit fly Drosophila melanogaster as a model, because it has the simplest type of airways, consisting of epithelial cells only. Elucidating the structure of the innate immune system of this "airway epithelial cell culture" might enable us to understand why deregulatory processes in innate immune signalling cascades lead to long lasting inflammatory events.
All airway epithelial cells of the fruit fly are able to launch an immune response. They contain only one functional signal transduction pathway that converges onto NF-kappaB factors, namely the IMD-pathway, which is homologous to the TNF-alpha receptor pathway. Although vital parts of the Toll-pathway are missing, dorsal and dif, the NF-kappaB factors dedicated to this signalling system, are present. Other pathways involved in immune regulation, such as the JNK- and the JAK/STAT-pathway, are completely functional in these cells. In addition, most peptidoglycan recognition proteins, representing the almost complete collection of pattern recognition receptors, are part of the epithelial cells equipment. Potential effector molecules are different antimicrobial peptides and lysozymes, but also transferrin that can inhibit bacterial growth through iron-depletion. Reactive oxygen species can be inactivated through the almost complete armamentarium of enzymatic antioxidants that has the fly to its disposal.
The innate immune system of the fly's airway epithelium has a very peculiar organization. A great variety of pattern recognition receptors as well as of potential effector molecules are conspicuous, whereas signalling presumably occurs through a single NF-kappaB activating pathway. This architecture will allow reacting if confronted with different bacterial or fungal elicitors by activation of a multitude of effectors.
气道上皮细胞不仅构成物理屏障,也是抵御空气传播病原体的第一道防线。同时,它们不断暴露于活性氧中。因此,气道上皮细胞必须拥有复杂的固有免疫系统和分子武器库来清除活性氧。很明显,上皮固有免疫失调是慢性炎症性肺病发生发展的主要原因。为阐明气道上皮细胞固有免疫系统的分子结构,我们选择果蝇作为模型,因为它具有最简单的气道类型,仅由上皮细胞组成。阐明这种“气道上皮细胞培养物”的固有免疫系统结构,可能使我们理解为什么固有免疫信号级联中的失调过程会导致持久的炎症事件。
果蝇的所有气道上皮细胞都能够启动免疫反应。它们仅包含一条汇聚到核因子κB因子上的功能性信号转导途径,即IMD途径,该途径与肿瘤坏死因子α受体途径同源。尽管Toll途径的重要部分缺失,但负责该信号系统的核因子κB因子背侧蛋白和Dif存在。参与免疫调节的其他途径,如JNK途径和JAK/STAT途径,在这些细胞中完全发挥功能。此外,代表几乎完整模式识别受体集合的大多数肽聚糖识别蛋白是上皮细胞装备的一部分。潜在的效应分子包括不同的抗菌肽和溶菌酶,还有能通过缺铁抑制细菌生长的转铁蛋白。活性氧可通过果蝇所拥有的几乎完整的酶促抗氧化剂武器库失活。
果蝇气道上皮的固有免疫系统具有非常独特的组织形式。多种模式识别受体以及潜在的效应分子很显著,而信号传导可能通过单一的核因子κB激活途径发生。这种结构将允许在面对不同的细菌或真菌激发子时通过激活多种效应分子做出反应。