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缓激肽介导的炎症信号网络的模块化图谱。

A modular map of Bradykinin-mediated inflammatory signaling network.

作者信息

Rex D A B, Deepak K, Vaid Neelanchal, Dagamajalu Shobha, Kandasamy Richard Kumaran, Flo Trude Helen, Keshava Prasad T S

机构信息

Center for Systems Biology and Molecular Medicine, Yenepoya Research Centre, Yenepoya (Deemed to be University), Mangalore, 575018, India.

Centre of Molecular Inflammation Research (CEMIR), and Department of Clinical and Molecular Medicine (IKOM), Norwegian University of Science and Technology, 7491, Trondheim, Norway.

出版信息

J Cell Commun Signal. 2022 Jun;16(2):301-310. doi: 10.1007/s12079-021-00652-0. Epub 2021 Oct 29.

Abstract

Bradykinin, a member of the kallikrein-kinin system (KKS), is associated with an inflammatory response pathway with diverse vascular permeability functions, including thrombosis and blood coagulation. In majority, bradykinin signals through Bradykinin Receptor B2 (B2R). B2R is a G protein-coupled receptor (GPCR) coupled to G protein family such as Gα, Gα/Gα Gα and Gβ12 B2R stimulation leads to the activation of a signaling cascade of downstream molecules such as phospholipases, protein kinase C, Ras/Raf-1/MAPK, and PI3K/AKT and secondary messengers such as inositol-1,4,5-trisphosphate, diacylglycerol and Ca ions. These secondary messengers modulate the production of nitric oxide or prostaglandins. Bradykinin-mediated signaling is implicated in inflammation, chronic pain, vasculopathy, neuropathy, obesity, diabetes, and cancer. Despite the biomedical importance of bradykinin, a resource of bradykinin-mediated signaling pathway is currently not available. Here, we developed a pathway resource of signaling events mediated by bradykinin. By employing data mining strategies in the published literature, we describe an integrated pathway reaction map of bradykinin consisting of 233 reactions. Bradykinin signaling pathway events included 25 enzyme catalysis reactions, 12 translocations, 83 activation/inhibition reactions, 11 molecular associations, 45 protein expression and 57 gene regulation events. The pathway map is made publicly available on the WikiPathways Database with the ID URL: https://www.wikipathways.org/index.php/Pathway:WP5132 . The bradykinin-mediated signaling pathway map will facilitate the identification of novel candidates as therapeutic targets for diseases associated with dysregulated bradykinin signaling.

摘要

缓激肽是激肽释放酶 - 激肽系统(KKS)的成员,与具有多种血管通透性功能的炎症反应途径相关,包括血栓形成和血液凝固。在大多数情况下,缓激肽通过缓激肽受体B2(B2R)发出信号。B2R是一种与G蛋白家族(如Gα、Gαi/Gαo和Gβ1γ2)偶联的G蛋白偶联受体(GPCR)。B2R的刺激会导致下游分子的信号级联激活,如磷脂酶、蛋白激酶C、Ras/Raf-1/MAPK和PI3K/AKT,以及第二信使如肌醇-1,4,5-三磷酸、二酰甘油和钙离子。这些第二信使调节一氧化氮或前列腺素的产生。缓激肽介导的信号传导与炎症、慢性疼痛、血管病变、神经病变、肥胖、糖尿病和癌症有关。尽管缓激肽具有重要的生物医学意义,但目前尚无缓激肽介导的信号通路资源。在此,我们开发了一种由缓激肽介导的信号事件的通路资源。通过在已发表的文献中采用数据挖掘策略,我们描述了一个由233个反应组成的缓激肽综合通路反应图。缓激肽信号通路事件包括25个酶催化反应、12个易位、83个激活/抑制反应、11个分子缔合、45个蛋白质表达和57个基因调控事件。该通路图已在WikiPathways数据库上公开提供,ID网址为:https://www.wikipathways.org/index.php/Pathway:WP5132 。缓激肽介导的信号通路图将有助于识别新的候选物,作为与缓激肽信号失调相关疾病的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a26e/8891415/41b7ee99ba60/12079_2021_652_Fig1_HTML.jpg

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