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CD28 Signaling Augments Elk-1-Dependent Transcription at the c-fosGene During Antigen Stimulation
Author(s) -
Wei Li,
Carmella D. Whaley,
Jody Bonnevier,
Anna Mondino,
Molly E. Martin,
Kjersti AagaardTillery,
Daniel L. Mueller
Publication year - 2001
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.167.2.827
Subject(s) - transactivation , cd28 , kinase , microbiology and biotechnology , signal transduction , biology , stimulation , c jun , immediate early gene , gene expression , chemistry , transcription factor , t cell , gene , immunology , immune system , biochemistry , endocrinology
Untransformed CD4(+) Th1 cells stimulated with Ag and APC demonstrated a dependence on B7- and CD28-mediated costimulatory signals for the expression and function of AP-1 proteins. The induction of transactivation by the c-fos gene regulator Elk-1 mirrored this requirement for TCR and CD28 signal integration. c-Jun N-terminal kinase (JNK) (but not extracellular signal-regulated kinase or p38) protein kinase activity was similarly inhibited by neutralizing anti-B7 mAbs. Blockade of JNK protein kinase activity with SB 202190 prevented both Elk-1 transactivation and c-Fos induction. These results identify a unique role for B7 costimulatory molecules and CD28 in the activation of JNK during Ag stimulation in Th1 cells, and suggest that JNK regulates Elk-1 transactivation at the c-fos gene to promote the formation of AP-1 complexes important to IL-2 gene expression.

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