| Literature DB >> 15607792 |
Ann Sophie Franki1, Katrien Van Beneden, Pieter Dewint, Ivan Meeus, Eric Veys, Dieter Deforce, Dirk Elewaut.
Abstract
Lymphotoxin (LT) alpha 1 beta 2, a tumour necrosis factor (TNF) cytokine critically involved in lymphoid organogenesis, is indispensable for the differentiation of V alpha 14i natural killer T (NKT) cells, a lymphocyte subset with important immunoregulatory properties. However, it is not required for the development of conventional T-cells. LT alpha 1 beta 2 signals through the LT beta receptor, which is expressed on non-lymphoid cells. Triggering of this receptor induces a unique signalling cascade leading to the activation of the transcription factor RelB through activation of NF-kappa B inducing kinase. This pathway is required for V alpha 14i NKT cell differentiation as appears from studies in gene-deficient animals. By reciprocal bone marrow chimeras, it was shown that RelB is required in a radiation-resistant host cell or stromal cell for normal V alpha 14i NKT cell development, presumably in the thymic stroma. These stromal cells are not required for the positive selection of these cells but rather play a prominent role in their terminal differentiation. Altogether, these observations underscore the unique developmental requirements of this particular lymphocyte subset.Entities:
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Year: 2005 PMID: 15607792 DOI: 10.1016/j.molimm.2004.07.020
Source DB: PubMed Journal: Mol Immunol ISSN: 0161-5890 Impact factor: 4.407