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A Role for Stat5 in CD8+ T Cell Homeostasis
Author(s) -
John A. Kelly,
Rosanne Spolski,
Kazunori Imada,
Julie Bollenbacher,
Stephen Lee,
Warren J. Leonard
Publication year - 2003
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.170.1.210
Subject(s) - stat5 , cd8 , homeostasis , microbiology and biotechnology , cytotoxic t cell , t cell , biology , transgene , cytokine , signal transduction , immunology , immune system , biochemistry , gene , in vitro
Cytokine signals are known to contribute to CD8+ memory T cell homeostasis, but an exact understanding of the mechanism(s) has remained elusive. We have now investigated the role of Stat5 proteins in this process. Whereas Stat5a and Stat5b KO mice have decreased numbers of CD8+ T cells, Stat5-transgenic mice have an increased number of these cells. Stat5b-transgenic mice exhibit increased Ag-induced cell death of CD4+ T cells and augmented proliferation and Bcl-2 expression in CD8+ T cells, providing a basis for this finding. Moreover, CD8+ memory T cells are substantially affected by Stat5 levels. These findings identify Stat5 proteins as critical signaling mediators used by cytokines to regulate CD8+ T cell homeostasis.

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