炎性小体信号传导的因果生物学网络模型用于解释各种炎症状态的转录组变化。

IF 2.6 Q3 IMMUNOLOGY
International Journal of Inflammation Pub Date : 2022-01-27 eCollection Date: 2022-01-01 DOI:10.1155/2022/4071472
Hasmik Yepiskoposyan, Manuel C Peitsch, Marja Talikka
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引用次数: 1

摘要

实际上,任何改变细胞内稳态的应激源都可能导致炎症反应。炎性小体作为先天免疫的重要组成部分,在炎症反应中发挥着重要作用。关于炎性体生物学的信息正在迅速增长,因此需要将其构建成一个模型,以帮助可视化和增强对潜在生物学过程的理解。因果生物网络(CBN)模型为新的疾病机制和治疗结果提供了预测能力。我们将炎性体激活的现有文献信息整合到CBN模型中,并使用公开可用的转录组数据集对其进行评分,这些数据集涉及肺部病毒感染、骨关节炎和类风湿关节炎、牛皮癣和衰老。评分推断通路激活导致NLRP3炎症小体在这些不同条件下激活,表明CBN模型为解释炎症小体激活背景下的转录组数据提供了一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Causal Biological Network Model for Inflammasome Signaling Applied for Interpreting Transcriptomic Changes in Various Inflammatory States.

Causal Biological Network Model for Inflammasome Signaling Applied for Interpreting Transcriptomic Changes in Various Inflammatory States.

Causal Biological Network Model for Inflammasome Signaling Applied for Interpreting Transcriptomic Changes in Various Inflammatory States.

Causal Biological Network Model for Inflammasome Signaling Applied for Interpreting Transcriptomic Changes in Various Inflammatory States.

Virtually any stressor that alters the cellular homeostatic state may result in an inflammatory response. As a critical component of innate immunity, inflammasomes play a prominent role in the inflammatory response. The information on inflammasome biology is rapidly growing, thus creating the need for structuring it into a model that can help visualize and enhance the understanding of underlying biological processes. Causal biological network (CBN) models provide predictive power for novel disease mechanisms and treatment outcomes. We assembled the available literature information on inflammasome activation into the CBN model and scored it with publicly available transcriptomic datasets that address viral infection of the lungs, osteo- and rheumatoid arthritis, psoriasis, and aging. The scoring inferred pathway activation leading to NLRP3 inflammasome activation in these diverse conditions, demonstrating that the CBN model provides a platform for interpreting transcriptomic data in the context of inflammasome activation.

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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
16
审稿时长
16 weeks
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