CD28 Signaling Augments Elk-1-Dependent Transcription at the c- fos Gene During Antigen Stimulation

  • Li W
  • Whaley C
  • Bonnevier J
  • et al.
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Abstract

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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APA

Li, W., Whaley, C. D., Bonnevier, J. L., Mondino, A., Martin, M. E., Aagaard-Tillery, K. M., & Mueller, D. L. (2001). CD28 Signaling Augments Elk-1-Dependent Transcription at the c- fos Gene During Antigen Stimulation. The Journal of Immunology, 167(2), 827–835. https://doi.org/10.4049/jimmunol.167.2.827

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