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巨噬细胞激活核心信号通路的基于逻辑的示意图。

A logic-based diagram of signalling pathways central to macrophage activation.

作者信息

Raza Sobia, Robertson Kevin A, Lacaze Paul A, Page David, Enright Anton J, Ghazal Peter, Freeman Tom C

机构信息

Division of Pathway Medicine, University of Edinburgh, The Chancellor's Building, College of Medicine, 49 Little France Crescent, Edinburgh, EH16 4SB, UK.

出版信息

BMC Syst Biol. 2008 Apr 23;2:36. doi: 10.1186/1752-0509-2-36.

Abstract

BACKGROUND

The complex yet flexible cellular response to pathogens is orchestrated by the interaction of multiple signalling and metabolic pathways. The molecular regulation of this response has been studied in great detail but comprehensive and unambiguous diagrams describing these events are generally unavailable. Four key signalling cascades triggered early-on in the innate immune response are the toll-like receptor, interferon, NF-kappaB and apoptotic pathways, which co-operate to defend cells against a given pathogen. However, these pathways are commonly viewed as separate entities rather than an integrated network of molecular interactions.

RESULTS

Here we describe the construction of a logically represented pathway diagram which attempts to integrate these four pathways central to innate immunity using a modified version of the Edinburgh Pathway Notation. The pathway map is available in a number of electronic formats and editing is supported by yEd graph editor software.

CONCLUSION

The map presents a powerful visual aid for interpreting the available pathway interaction knowledge and underscores the valuable contribution well constructed pathway diagrams make to communicating large amounts of molecular interaction data. Furthermore, we discuss issues with the limitations and scalability of pathways presented in this fashion, explore options for automated layout of large pathway networks and demonstrate how such maps can aid the interpretation of functional studies.

摘要

背景

细胞对病原体的复杂而灵活的反应是由多种信号传导和代谢途径的相互作用所协调的。虽然对这种反应的分子调控已经进行了详细研究,但描述这些事件的全面且明确的图表通常并不存在。在先天免疫反应早期触发的四个关键信号级联是Toll样受体、干扰素、核因子κB和凋亡途径,它们共同协作以保护细胞抵御特定病原体。然而,这些途径通常被视为独立的实体,而非分子相互作用的整合网络。

结果

在此,我们描述了一个逻辑表示的途径图的构建,该图尝试使用爱丁堡途径表示法的修改版本来整合先天免疫核心的这四个途径。该途径图有多种电子格式可供使用,并且由yEd图形编辑器软件支持编辑。

结论

该图为解释可用的途径相互作用知识提供了强大的视觉辅助工具,并强调了构建良好的途径图在传达大量分子相互作用数据方面的宝贵贡献。此外,我们讨论了以这种方式呈现的途径的局限性和可扩展性问题,探索了大型途径网络自动布局的选项,并展示了此类图如何有助于功能研究的解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/748f/2383880/e3d513ed24ef/1752-0509-2-36-1.jpg

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