| Literature DB >> 11160211 |
Q Wu1, Y Sun, J Wang, X Lin, Y Wang, L E Pegg, A Fütterer, K Pfeffer, Y X Fu.
Abstract
NK cells play an important role in the immune system but the cellular and molecular requirements for their early development are poorly understood. Lymphotoxin-alpha (LTalpha)(-/-) and LTbetaR(-/-) mice show a severe systemic reduction of NK cells, which provides an excellent model to study NK cell development. In this study, we show that the bone marrow (BM) or fetal liver cells from LTalpha(-/-) or LTbetaR(-/-) mice efficiently develop into mature NK cells in the presence of stromal cells from wild-type mice but not from LTalpha(-/-) or LTbetaR(-/-) mice. Direct activation of LTbetaR-expressing BM stromal cells is shown to promote to early NK cell development in vitro. Furthermore, the blockade of the interaction between LT and LTbetaR in adult wild-type mice by administration of LTbetaR-Ig impairs the development of NK cells in vivo. Together, these results indicate that the signal via LTbetaR on BM stromal cells by membrane LT is an important pathway for early NK cell development.Entities:
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Year: 2001 PMID： 11160211 DOI： 10.4049/jimmunol.166.3.1684
Source DB: PubMed Journal: J Immunol ISSN： 0022-1767 Impact factor: 5.422