| Literature DB >> 20194894 |
Amy Saunders1, Louise M C Webb, Michelle L Janas, Amanda Hutchings, John Pascall, Christine Carter, Nicholas Pugh, Geoff Morgan, Martin Turner, Geoffrey W Butcher.
Abstract
The guanosine triphosphatases (GTPases) of the immunity-associated protein (GIMAP) family of putative GTPases has been implicated in the regulation of T-lymphocyte development and survival. A mouse conditional knockout allele was generated for the immune GTPase gene GIMAP1. Homozygous loss of this allele under the influence of the lymphoid-expressed hCD2-iCre recombinase transgene led to severe (> 85%) deficiency of mature T lymphocytes and, unexpectedly, of mature B lymphocytes. By contrast there was little effect of GIMAP1 deletion on immature lymphocytes in either B or T lineages, although in vitro studies showed a shortening of the survival time of both immature and mature CD4(+) single-positive thymocytes. These findings show a vital requirement for GIMAP1 in mature lymphocyte development/survival and draw attention to the nonredundant roles of members of the GIMAP GTPase family in these processes.Entities:
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Year: 2010 PMID: 20194894 DOI: 10.1182/blood-2009-08-237586
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113