Innate immune cell CD45 regulates lymphopenia-induced T cell proliferation

Amy E. Saunders, Yaein A. Shim, Pauline Johnson

    Research output: Contribution to journalArticlepeer-review


    © 2014 by The American Association of Immunologists, Inc.The leukocyte-specific tyrosine phosphatase, CD45, severely impacts T cell development and activation by modulating TCR signaling. CD45-deficient (CD45KO) mice have reduced peripheral T cell numbers where CD8 T cells are underrepresented. In this article, we show that CD45KO mice are unable to support efficient homeostatic proliferation, affecting CD8 T cells more than CD4 T cells. Using CD45-RAG1 double-deficient (45RAGKO) mice, we show that lymphopenia-induced proliferation (LIP) of CD45- sufficient T cells is defective in a host environment lacking CD45 on innate immune cells. We identify two deficiencies in the 45RAGKO mice that affect LIP. One involves CD11c+cells and the second the production of IL-7 by lymphoid stromal cells. CD45KO dendritic cells were not defective in foreign Ag-induced T cell proliferation, yet CD45KO CD11c+cells were unable to rescue the spontaneous LIP in the 45RAGKO mice. This was in contrast with the CD45-sufficient CD11c+cells that partially rescued this spontaneous proliferation and did so without affecting IL-7 levels. The absence of CD45 also led to reduced IL-7 production by lymphoid stromal cells, suggesting an indirect effect of CD45 on innate immune cells in influencing IL-7 production by lymphoid stromal cells. These findings demonstrate a novel role for CD45 on innate immune cells in promoting lymphopeniainduced T cell proliferation and suggest that innate immune cells may communicate with stromal cells to regulate IL-7 production.
    Original languageEnglish
    Pages (from-to)2831-2842
    Number of pages11
    JournalJournal of Immunology
    Issue number6
    Publication statusPublished - 15 Sept 2014


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