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Journal of Experimental Medicine, Vol 179, 177-184, Copyright © 1994 by Rockefeller University Press
ARTICLES |
MR Hough, F Takei, RK Humphries and R Kay
Terry Fox Laboratory, British Columbia Cancer Agency, Vancouver, Canada.
Heat-stable antigen (HSA) is a small, glycosyl phosphatidylinositol- anchored protein that can act as a costimulatory molecule for antigen- dependent activation of helper T cells. In addition to being expressed on antigen-presenting B cells, HSA is also expressed during the initial stages of T cell development in the thymus. HSA levels are very high on immature CD4-, CD8- double negative thymocytes, but are reduced on CD4+, CD8+ double positive cells undergoing selection in the thymus, and are entirely eliminated when these cells differentiate into immunologically competent CD4+ or CD8+ single positive T cells. To examine the potential roles of this molecule in T cell development and selection, we generated transgenic mice in which HSA was highly expressed on all classes of thymocytes. The consequence of deregulated HSA expression was a pronounced reduction in the numbers of double positive and single positive thymocytes, whereas the numbers of their double negative precursors were largely unaffected. These results demonstrate that downregulation of HSA expression at the double positive stage is a critical event in thymocyte development. The depletion of thymocytes resulting from HSA overexpression begins at the same time as the onset of negative selection, suggesting that HSA may provide signals that contribute to determining the efficiency of this process.
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