Identification of an IL-7-Dependent Pre-T Committed Population in the Spleen
Author(s) -
Laetitia GautreauRolland,
Marie-Laure Arcangeli,
Valérie Pasqualetto,
AnneMarie Joret,
Corinne Cordier,
Jérôme Mégret,
Elke Schneider,
Sophie Ezine
Publication year - 2007
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.179.5.2925
Subject(s) - spleen , biology , progenitor cell , t cell , population , microbiology and biotechnology , il 2 receptor , immunology , interleukin 3 , myeloid , lymphopoiesis , progenitor , thymectomy , stem cell , immune system , medicine , myasthenia gravis , environmental health
Several extrathymic T cell progenitors have been described but their various contributions to the T cell lineage puzzle are unclear. In this study, we provide evidence for a splenic Lin(-)Thy1.2(+) T cell-committed population, rare in B6 mice, abundant in TCRalpha(-/-), CD3epsilon(-/-), and nude mice, and absent in IL-7- and Rag-2-deficient mice. Neither B nor myeloid cells are generated in vivo and in vitro. The incidence of these pre-T cells is under the control of thymus and/or mature T cells, as revealed by graft experiments. Indeed, IL-7 consumption by mature T cells inhibits the growth of these pre-T cells. Moreover, the nude spleen contains an additional Lin(-)Thy1.2(+)CD25(+) subset which is detected in B6 mice only after thymectomy. We establish that the full pre-T cell potential and proliferation capacity are only present in the c-kit(low) fraction of progenitors. We also show that most CCR9(+) progenitors are retained in the spleen of nude mice, but present in the blood of B6 mice. Thus, our data describe a new T cell lineage restricted subset that accumulates in the spleen before migration to the thymus.
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