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A modular map of Bradykinin-mediated inflammatory signaling network

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 re...

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Autores principales: Rex, D. A. B., Deepak, K., Vaid, Neelanchal, Dagamajalu, Shobha, Kandasamy, Richard Kumaran, Flo, Trude Helen, Keshava Prasad, T. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554507/
https://www.ncbi.nlm.nih.gov/pubmed/34714516
http://dx.doi.org/10.1007/s12079-021-00652-0
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author Rex, D. A. B.
Deepak, K.
Vaid, Neelanchal
Dagamajalu, Shobha
Kandasamy, Richard Kumaran
Flo, Trude Helen
Keshava Prasad, T. S.
author_facet Rex, D. A. B.
Deepak, K.
Vaid, Neelanchal
Dagamajalu, Shobha
Kandasamy, Richard Kumaran
Flo, Trude Helen
Keshava Prasad, T. S.
author_sort Rex, D. A. B.
collection PubMed
description 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(qs), Gα(q)/Gα(11,) Gα(i1,) and Gβ1(γ)2(.) 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(2+) 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12079-021-00652-0.
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spelling pubmed-85545072021-10-29 A modular map of Bradykinin-mediated inflammatory signaling network Rex, D. A. B. Deepak, K. Vaid, Neelanchal Dagamajalu, Shobha Kandasamy, Richard Kumaran Flo, Trude Helen Keshava Prasad, T. S. J Cell Commun Signal Nuts and Bolts 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(qs), Gα(q)/Gα(11,) Gα(i1,) and Gβ1(γ)2(.) 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(2+) 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12079-021-00652-0. Springer Netherlands 2021-10-29 2022-06 /pmc/articles/PMC8554507/ /pubmed/34714516 http://dx.doi.org/10.1007/s12079-021-00652-0 Text en © The International CCN Society 2021
spellingShingle Nuts and Bolts
Rex, D. A. B.
Deepak, K.
Vaid, Neelanchal
Dagamajalu, Shobha
Kandasamy, Richard Kumaran
Flo, Trude Helen
Keshava Prasad, T. S.
A modular map of Bradykinin-mediated inflammatory signaling network
title A modular map of Bradykinin-mediated inflammatory signaling network
title_full A modular map of Bradykinin-mediated inflammatory signaling network
title_fullStr A modular map of Bradykinin-mediated inflammatory signaling network
title_full_unstemmed A modular map of Bradykinin-mediated inflammatory signaling network
title_short A modular map of Bradykinin-mediated inflammatory signaling network
title_sort modular map of bradykinin-mediated inflammatory signaling network
topic Nuts and Bolts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8554507/
https://www.ncbi.nlm.nih.gov/pubmed/34714516
http://dx.doi.org/10.1007/s12079-021-00652-0
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