Abstract
Lymphotoxin β receptor (LTβR) signaling is crucial for lymphoid tissue organogenesis and immune homeostasis. To identify novel regulatory mechanisms for signaling, we implemented a two-step screen that uses coexpression analysis of human fibroblasts undergoing LTβR stimulation and affinity-purification mass spectrometry for the LTβR signaling protein TNFR-associated factor 3 (TRAF3). We identify Ewing sarcoma (EWS) protein as a novel LTβR signaling component that associates with TRAF3 but not with TNFR-associated factor 2 (TRAF2). The EWS:TRAF3 complex forms under unligated conditions that are disrupted following activation of the LTβR. We conclude that EWS limits expression of proinflammatory molecules, GM-CSF, and ERK-2, promoting immune homeostasis.
Copyright © 2020 by The American Association of Immunologists, Inc.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Granulocyte-Macrophage Colony-Stimulating Factor / genetics
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Granulocyte-Macrophage Colony-Stimulating Factor / immunology
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HEK293 Cells
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Humans
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Lymphotoxin beta Receptor / genetics
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Lymphotoxin beta Receptor / immunology*
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MAP Kinase Signaling System / genetics
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MAP Kinase Signaling System / immunology*
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Mitogen-Activated Protein Kinase 1 / genetics
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Mitogen-Activated Protein Kinase 1 / immunology
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Multiprotein Complexes / genetics
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Multiprotein Complexes / immunology*
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RNA-Binding Protein EWS / genetics
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RNA-Binding Protein EWS / immunology*
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TNF Receptor-Associated Factor 2 / genetics
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TNF Receptor-Associated Factor 2 / immunology
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TNF Receptor-Associated Factor 3 / genetics
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TNF Receptor-Associated Factor 3 / immunology
Substances
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EWSR1 protein, human
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LTBR protein, human
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Lymphotoxin beta Receptor
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Multiprotein Complexes
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PSMD2 protein, human
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RNA-Binding Protein EWS
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TNF Receptor-Associated Factor 2
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TNF Receptor-Associated Factor 3
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TRAF3 protein, human
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Granulocyte-Macrophage Colony-Stimulating Factor
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MAPK1 protein, human
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Mitogen-Activated Protein Kinase 1