Tumor Necrosis Factor Receptor-Associated Factor Regulation of Nuclear Factor κB and Mitogen-Activated Protein Kinase Pathways
Tumor necrosis factor receptor (TNFR)-associated factors (TRAFs) are a family of structurally related proteins that transduces signals from members of TNFR superfamily and various other immune receptors. Major downstream signaling events mediated by the TRAF molecules include activation of the trans...
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Published in | Frontiers in immunology Vol. 9; p. 1849 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
09.08.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Tumor necrosis factor receptor (TNFR)-associated factors (TRAFs) are a family of structurally related proteins that transduces signals from members of TNFR superfamily and various other immune receptors. Major downstream signaling events mediated by the TRAF molecules include activation of the transcription factor nuclear factor κB (NF-κB) and the mitogen-activated protein kinases (MAPKs). In addition, some TRAF family members, particularly TRAF2 and TRAF3, serve as negative regulators of specific signaling pathways, such as the noncanonical NF-κB and proinflammatory toll-like receptor pathways. Thus, TRAFs possess important and complex signaling functions in the immune system and play an important role in regulating immune and inflammatory responses. This review will focus on the role of TRAF proteins in the regulation of NF-κB and MAPK signaling pathways. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 Specialty section: This article was submitted to Molecular Innate Immunity, a section of the journal Frontiers in Immunology Reviewed by: Hasem Habelhah, University of Iowa, United States; Ping Xie, Rutgers University, The State University of New Jersey, United States; Weizhou Zhang, University of Iowa, United States Edited by: Gail Abendroth Bishop, University of Iowa, United States |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2018.01849 |