Ly-6A is a murine antigen which is implicated in lymphocyte activation and may be involved in activation of hematopoietic stem cells. Antibody cross-linking studies and antisense experiments have suggested that Ly-6A is a lymphocyte coactivation molecule. To better understand the function of Ly-6A, we used gene targeting to produce Ly-6A null mice which are healthy and have normal numbers and percentages of hematopoietic lineages. However, T lymphocytes from Ly-6A–deficient animals proliferate at a significantly higher rate in response to antigens and mitogens than wild-type littermates. In addition, Ly-6A mutant splenocytes generate more cytotoxic T lymphocytes compared to wild-type splenocytes when cocultured with alloantigen. This enhanced proliferation is not due to alterations in kinetics of response, sensitivity to stimulant concentration, or cytokine production by the T cell population, and is manifest in both in vivo and in vitro T cell responses. Moreover, T cells from Ly-6A–deficient animals exhibit a prolonged proliferative response to antigen stimulation, thereby suggesting that Ly-6A acts to downmodulate lymphocyte responses.
Altered Proliferative Response by T Lymphocytes of Ly-6A (Sca-1) Null Mice
Address correspondence to Dr. Patrick M. Flood, Department of Microbiology and Immunology, Curriculum in Oral Biology, Dental Research Center, University of North Carolina, Chapel Hill, NC 27599-7455. Phone: 919-966-1538; FAX: 919-966-3683; E-mail: [email protected]. W.L. Stanford's present address is Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario M5G 1X5, Canada.
Abbreviations used in this paper: Con A, Concanavalin A; ES, embryonic stem; GANC, gancyclovir; GPI, glycosyl phosphatidylinositol; SSLP, simple sequence length polymorphism.
William L. Stanford, Salma Haque, Robert Alexander, Xuemei Liu, Anne M. Latour, H. Ralph Snodgrass, Beverly H. Koller, Patrick M. Flood; Altered Proliferative Response by T Lymphocytes of Ly-6A (Sca-1) Null Mice . J Exp Med 29 August 1997; 186 (5): 705–717. doi: https://doi.org/10.1084/jem.186.5.705
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