Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1989 Dec;86(24):10064-8.
doi: 10.1073/pnas.86.24.10064.

Overexpression of src family gene for tyrosine-kinase p59fyn in CD4-CD8- T cells of mice with a lymphoproliferative disorder

Affiliations

Overexpression of src family gene for tyrosine-kinase p59fyn in CD4-CD8- T cells of mice with a lymphoproliferative disorder

T Katagiri et al. Proc Natl Acad Sci U S A. 1989 Dec.

Erratum in

  • Proc Natl Acad Sci U S A 1990 Apr;87(7):2865

Abstract

Overexpression of a src family gene, lck, has been associated with differentiation of the murine thymic lymphoma line LSTRA. Recent findings by several groups strongly suggest a functional role for the gene product p56lck protein-tyrosine kinase (PTK) in the activation of normal T cells. A single recessive gene, lpr or gld, induces a lymphoproliferative disorder concomitant with autoimmune disease in mice. In this study, a 10-fold elevated activity of PTK encoded by fyn, another src family gene, was demonstrated in CD4-CD8- T cells in mutant mice. The increased PTK activity was consistent with overexpression of fyn mRNA. The elevated fyn mRNA expression appeared to be a characteristic of CD4-CD8- T cells, since it was not observed in normal T cells at any stage of differentiation. The fact that fyn mRNA expression was markedly induced in normal T cells by mitogenic stimulation with anti-T3 epsilon antiserum supports the possibility that p59fyn PTK is a signal-generating molecule in T cells. Thus, our findings provide insight into the physiological role for a src gene family kinase in T-cell development and contribute to a better understanding of the molecular mechanisms of disease-inducing recessive genes.

PubMed Disclaimer

References

    1. J Biol Chem. 1988 May 25;263(15):6956-9 - PubMed
    1. J Exp Med. 1988 Mar 1;167(3):741-51 - PubMed
    1. Proc Natl Acad Sci U S A. 1988 Jul;85(14):5190-4 - PubMed
    1. J Immunol. 1988 Aug 15;141(4):1120-5 - PubMed
    1. Cell. 1988 Oct 21;55(2):301-8 - PubMed

Publication types

MeSH terms