Profound block in thymocyte development in mice lacking p56lck - PubMed (original) (raw)
. 1992 May 14;357(6374):161-4.
doi: 10.1038/357161a0.
Affiliations
- PMID: 1579166
- DOI: 10.1038/357161a0
Profound block in thymocyte development in mice lacking p56lck
T J Molina et al. Nature. 1992.
Abstract
The protein Lck (p56lck) has a relative molecular mass of 56,000 and belongs to the Src family of tyrosine kinases. It is expressed exclusively in lymphoid cells, predominantly in thymocytes and peripheral T cells. Lck associates specifically with the cytoplasmic domains of both CD4 and CD8 T-cell surface glycoproteins and interacts with the beta-chain of the interleukin-2 receptor, which implicates Lck activity in signal transduction during thymocyte ontogeny and activation of mature T cells. Here we generate an lck null mutation by homologous recombination in embryonic stem cells to evaluate the role of p56lck in T-cell development and activation. Lck-deficient mice show a pronounced thymic atrophy, with a dramatic reduction in the double-positive (CD4+CD8+) thymocyte population. Mature, single-positive thymocytes are not detectable in these mice and there are only very few peripheral T cells. These results illustrate the crucial role of this T-cell-specific tyrosine kinase in the thymocyte development.
Comment in
- Early T-cell development.
Gutierrez-Ramos JC, Toribio ML, Martinez C. Gutierrez-Ramos JC, et al. Nature. 1993 Jan 21;361(6409):213. doi: 10.1038/361213a0. Nature. 1993. PMID: 8423850 No abstract available.
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