Abstract
During fetal life, CD4+CD3- lymphoid tissue inducer (LTi) cells are required for lymph node and Peyer's patch development in mice. In adult animals, CD4+CD3- cells are found in low numbers in lymphoid organs. Whether adult CD4+CD3- cells are LTi cells and are generated and maintained through cytokine signals has not been directly addressed. In this study we show that adult CD4+CD3 - cells adoptively transferred into neonatal CXCR5-/- mice induced the formation of intestinal lymphoid tissues, demonstrating for the first time their bona fide LTi function. Increasing IL-7 availability in wild-type mice either by IL-7 transgene expression or treatment with IL-7/anti-IL-7 complexes increased adult LTi cell numbers through de novo generation from bone marrow cells and increased the survival and proliferation of LTi cells. Our observations demonstrate that adult CD4 +lineage- cells are LTi cells and that the availability of IL-7 determines the size of the adult LTi cell pool.
Original language | English |
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Pages (from-to) | 2217-2221 |
Number of pages | 5 |
Journal | Journal of Immunology |
Volume | 183 |
Issue number | 4 |
DOIs | |
Publication status | Published - 15 Aug 2009 |