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Wiley, European Journal of Immunology, 8(29), p. 2376-2384, 1999

DOI: 10.1002/(sici)1521-4141(199908)29:08<2376::aid-immu2376>3.0.co;2-7

Wiley, European Journal of Immunology, 08(29), p. 2376-2384

DOI: 10.1002/(sici)1521-4141(199908)29:08<2376::aid-immu2376>3.3.co;2-z

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The CD45 tyrosine phosphatase regulates CD3-induced signal transduction and T cell development in recombinase-deficient mice: Restoration of pre-TCR function by active p56(lck)

Journal article published in 1999 by Sabine Pingel, Matthew Baker, Martin Turner ORCID, Nick Holmes, Denis R. Alexander
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

The pre-TCR complex regulates the transition from CD4(-)CD8(-) double-negative (DN) to CD4(+)CD8(+) double-positive (DP) thymocytes during T cell development. In CD45(-/-) mice there is an accumulation of DN cells, suggesting a possible role for CD45 in pre-TCR signaling. We therefore crossed CD45(-/-) with Rag-1(-/-) mice to investigate the signaling functions of the CD3 complex in DN thymocytes. Remarkably, treatment of Rag-1(-/-)/CD45(-/-) mice with a CD3 mAb caused maturation to the DP stage at only 3% of the level measured in Rag-1(-/-) mice. Furthermore, ligation of the CD3 complex on Rag-1(-/-) /CD45(-/-) thymocytes in vitro induced less tyrosine phosphorylation in specific proteins when compared to Rag-1(-/-) thymocytes. CD45(-/-) mice were also crossed with pLGFA mice expressing a constitutively active form of the lck tyrosine kinase which restored the DN to DP transition to near normal levels. Our results are consistent with a model in which CD45-activated p56(lck) is critical for pre-TCR signal transduction.