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The Journal of Immunology, Vol 154, Issue 8 3636-3643, Copyright © 1995 by American Association of Immunologists
ARTICLES |
G Anderson, KL Anderson, LA Conroy, TJ Hallam, NC Moore, JJ Owen and EJ Jenkinson
Department of Anatomy, Medical School, University of Birmingham, Edgbaston, United Kingdom.
We have used in vitro models of thymocyte positive and negative selection in conjunction with selective inhibitors of the TCR-mediated signaling cascade to investigate the intracellular signaling events that mediate these processes. We report that Ro 31.8425, a potent and selective inhibitor of protein kinase C, which blocks the activation of mature T cells in a dose-dependent fashion, has no effect on either positive or negative selection of CD4+8+ thymocytes. In contrast, cyclosporin A fails to prevent negative selection, but inhibits positive selection through a direct effect on developing thymocytes, rather than through the perturbation of stromal cell support. Thus, our data suggest that positive and negative selection may operate via distinct intracellular signaling pathways.
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