| Literature DB >> 16988660 |
Karin Pike-Overzet1, Dick de Ridder, Floor Weerkamp, Miranda R M Baert, Monique M Verstegen, Martijn H Brugman, Steven J Howe, Marcel J T Reinders, Adrian J Thrasher, Gerard Wagemaker, Jacques J M van Dongen, Frank J T Staal.
Abstract
The gene IL2RG encodes the gamma-chain of the interleukin-2 receptor and is mutated in patients with X-linked severe combined immune deficiency (X-SCID). Woods et al. report the development of thymus tumours in a mouse model of X-SCID after correction by lentiviral overexpression of IL2RG and claim that these were caused by IL2RG itself. Here we find that retroviral overexpression of IL2RG in human CD34+ cells has no effect on T-cell development, whereas overexpression of the T-cell acute lymphoblastic leukaemia (T-ALL) oncogene LMO2 leads to severe abnormalities. Retroviral expression of IL2RG may therefore not be directly oncogenic--rather, the restoration of normal signalling by the interleukin-7 receptor to X-SCID precursor cells allows progression of T-cell development to stages that are permissive for the pro-leukaemic effects of ectopic LMO2.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16988660 DOI: 10.1038/nature05218
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962