| Literature DB >> 31969387 |
Richard Virgen-Slane1, Ricardo G Correa1, Parham Ramezani-Rad2, Seth Steen-Fuentes1, Thiago Detanico1, Michael J DiCandido3, Jun Li3, Carl F Ware4.
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.Entities:
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Year: 2020 PMID: 31969387 PMCID: PMC7033016 DOI: 10.4049/jimmunol.1901260
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422