Survivin is an inhibitor of apoptosis protein that also functions during mitosis. It is expressed in all common tumors and tissues with proliferating cells, including thymus. To examine its role in apoptosis and proliferation, we generated two T cell–specific survivin-deficient mouse lines with deletion occurring at different developmental stages. Analysis of early deleting survivin mice showed arrest at the pre–T cell receptor proliferating checkpoint. Loss of survivin at a later stage resulted in normal thymic development, but peripheral T cells were immature and significantly reduced in number. In contrast to in vitro studies, loss of survivin does not lead to increased apoptosis. However, newborn thymocyte homeostatic and mitogen-induced proliferation of survivin-deficient T cells were greatly impaired. These data suggest that survivin is not essential for T cell apoptosis but is crucial for T cell maturation and proliferation, and survivin-mediated homeostatic expansion is an important physiological process of T cell development.
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5 January 2004
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December 29 2003
Essential Role of Survivin, an Inhibitor of Apoptosis Protein, in T Cell Development, Maturation, and Homeostasis
Zheng Xing,
Zheng Xing
1Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, CA 94720
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Edward M. Conway,
Edward M. Conway
2Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, University of Leuven, B-3000 Leuven, Belgium
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Chulho Kang,
Chulho Kang
1Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, CA 94720
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Astar Winoto
Astar Winoto
1Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, CA 94720
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Zheng Xing
1Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, CA 94720
Edward M. Conway
2Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, University of Leuven, B-3000 Leuven, Belgium
Chulho Kang
1Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, CA 94720
Astar Winoto
1Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, Berkeley, CA 94720
Address correspondence to Astar Winoto, Department of Molecular and Cell Biology, Division of Immunology and Cancer Research Laboratory, University of California at Berkeley, 469 LSA, Berkeley, CA 94720. Phone: (510) 642-0217; Fax: (510) 642-0468; email: [email protected]
Abbreviations used in this paper: 7-AAD, 7-amino actinomycin D; BrdU, 5-bromo-2-deoxyuridine; CFSE, carboxy fluorescein diacetate succinimidyl ester; DN, double negative; DP, double positive; ES, embryonic stem; HSA, heat-stable antigen; IAP, inhibitor of apoptosis protein; SP, single positive.
Received:
September 15 2003
Accepted:
November 12 2003
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2004
J Exp Med (2004) 199 (1): 69–80.
Article history
Received:
September 15 2003
Accepted:
November 12 2003
Citation
Zheng Xing, Edward M. Conway, Chulho Kang, Astar Winoto; Essential Role of Survivin, an Inhibitor of Apoptosis Protein, in T Cell Development, Maturation, and Homeostasis . J Exp Med 5 January 2004; 199 (1): 69–80. doi: https://doi.org/10.1084/jem.20031588
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