| Literature DB >> 19635901 |
Sandrine Schmutz1, Nabil Bosco, Stephane Chappaz, Onur Boyman, Hans Acha-Orbea, Rhodri Ceredig, Antonius G Rolink, Daniela Finke.
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.Entities:
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Year: 2009 PMID: 19635901 DOI: 10.4049/jimmunol.0802911
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422