4.3 Article

A network map of IL-33 signaling pathway

期刊

JOURNAL OF CELL COMMUNICATION AND SIGNALING
卷 12, 期 3, 页码 615-624

出版社

SPRINGER
DOI: 10.1007/s12079-018-0464-4

关键词

Immune response; Inflammation; NetSlim; Pro-inflammatory cytokine; Post-translational modifications; Protein-protein interactions

资金

  1. Department of Biotechnology (DBT), Government of India
  2. INSPIRE Faculty Award from Department of Science and Technology (DST), Government of India
  3. SERB Young Scientist award from Department of Science and Technology (DST), Government of India
  4. Council of Scientific and Industrial Research (CSIR), Government of India
  5. INSPIRE Fellowship from the Department of Science and Technology, Government of India

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Interleukin-33 (IL-33) is a member of the IL-1 family of cytokines that play a central role in the regulation of immune responses. Its release from epithelial and endothelial cells is mediated by pro-inflammatory cytokines, cell damage and by recognition of pathogen-associated molecular patterns (PAMPs). The activity of IL-33 is mediated by binding to the IL-33 receptor complex (IL-33R) and activation of NF-kappa B signaling via the classical MyD88/IRAK/TRAF6 module. IL-33 also induces the phosphorylation and activation of ERK1/2, JNK, p38 and PI3K/AKT signaling modules resulting in the production and release of proinflammatory cytokines. Aberrant signaling by IL-33 has been implicated in the pathogenesis of several acute and chronic inflammatory diseases, including asthma, atopic dermatitis, rheumatoid arthritis and ulcerative colitis among others. Considering the biomedical importance of IL-33, we developed a pathway resource of signaling events mediated by IL-33/IL33R in this study. Using data mined from the published literature, we describe an integrated pathway reaction map of IL-33/IL33R consisting of 681 proteins and 765 reactions. These include information pertaining to 19 physical interaction events, 740 enzyme catalysis events, 6 protein translocation events, 4 activation/inhibition events, 9 transcriptional regulators and 2492 gene regulation events. The pathway map is publicly available through NetPath (http://www.netpath.org/), a resource of human signaling pathways developed previously by our group. This resource will provide a platform to the scientific community in facilitating identification of novel therapeutic targets for diseases associated with dysregulated IL-33 signaling.

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