Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Science Signaling - Call For Papers

Site Tools

  • AAAS
  • Subscribe
  • Feedback

Site Search

Search Advanced

Sci. STKE, 17 February 2004
Vol. 2004, Issue 220, p. tw65
[DOI: 10.1126/stke.2202004TW65]

EDITORS' CHOICE

IMMUNOLOGY Forkhead and Autoimmunity

The forkhead family of transcription factors are involved in a variety of systems. The forkhead family member Foxj1 is thought to play a role in the immune system, but genetic deficiency of this factor proves lethal, making direct in vivo analysis difficult. To overcome this, Lin et al. devised a chimeric system in mice, in which effects of Foxj1 deficiency could be explored. In these chimeras, foxj1-/- T cells displayed an exaggerated inflammatory cytokine expression, which eventually generated systemic autoimmunity. Normal repression of cytokine production by Foxj1 resulted from inhibition of the transcriptional activator nuclear factor NF-{kappa}B, possibly via the up-regulation of the inhibitory NF-{kappa}B cofactor, I{kappa}B.

L. Lin, M. S. Spoor, A. J. Gerth, S. L. Brody, S. L. Peng, Modulation of TH1 activation and inflammation by the NF-{kappa}B repressor Foxj1. Science 303, 1017-1020 (2004). [Abstract] [Full Text]

Citation: Forkhead and Autoimmunity. Sci. STKE 2004, tw65 (2004).


ADVERTISEMENT
Click Me!

ADVERTISEMENT
Click Me!

To Advertise     Find Products


Science Signaling. ISSN 1937-9145 (pre-2008: Science's STKE. ISSN 1525-8882)