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Cutting Edge: NF-κB2 Is a Negative Regulator of Dendritic Cell Function
Author(s) -
Kendra Speirs,
Linda A. Lieberman,
Jorge Caamaño,
Christopher A. Hunter,
Phillip Scott
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.172.2.752
Subject(s) - relb , microbiology and biotechnology , regulator , mhc class i , immune system , dendritic cell , nf κb , transcription factor , biology , chemistry , major histocompatibility complex , nfkb1 , immunology , signal transduction , genetics , gene
RelB, a member of the NF-kappaB family of transcription factors, is essential for dendritic cell (DC) maturation. Recent findings indicate that RelB is exclusively regulated through its interaction with cytoplasmic NF-kappaB2/p100. The studies presented in this report show that DCs lacking NF-kappaB2 have dramatically enhanced RelB activity, associated with increased MHC class II and costimulatory molecule expression and an enhanced ability to induce CD4(+) T cell responses. These studies identify a novel role for NF-kappaB2 in the negative regulation of RelB-induced DC maturation, with critical consequences for the regulation of adaptive immune responses.

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