p94(fer) facilitates cellular recovery of gamma irradiated pre-T cells

S. Halachmy, O. Bern, L. Schreiber, M. Carmel, Y. Sharabi, J. Shoham, U. Nir

    Research output: Contribution to journalArticlepeer-review

    14 Scopus citations

    Abstract

    p94(fer) is a ubiquitous, nuclear and cytoplasmic tyrosine kinase, whose accumulation has been demonstrated in all mammalian cell lines analysed. In the present work, the p94(fer) expression profile was determined in cell lines which were not tested before. While being present in several hematopoietic and non hematopoietic cell lines including thymic stromal cells, the p94(fer) kinase could not be detected in pre-T and T cell lines. p94(fer) was also absent in pre-B line, but accumulated in these cells upon their induced development to antibody producing cells. This is in agreement with the absence of p94(fer) in primary thymic and splenic T lymphocytes and its induced accumulation in stimulated B cells. Relatively high p94(fer) levels were detected in primary thymic and splenic stromal cells. Ectopic expression of p94(fer) in pre-T cells slightly affected their cell cycle profile but it did not affect their apoptotic death which was induced by ionizing radiation. However, p94(fer) facilitated dramatically, the cellular recovery of gamma irradiated pre-T cells which have escaped the apoptotic death. The enhanced recovery of the irradiated, p94(fer) expressing pre-T cells, resulted most probably from their increased survival, rather than from a prominent change in their proliferation rate. The absence of p94(fer) from pre-B and pre-T cells, may thus contribute to the relative sensitivity of these cells to ionizing radiation and to their dependence on the functioning of other nuclear tyrosine kinasese.

    Original languageEnglish
    Pages (from-to)2871-2880
    Number of pages10
    JournalOncogene
    Volume14
    Issue number24
    DOIs
    StatePublished - 19 Jun 1997

    Bibliographical note

    Funding Information:
    We thank U Caro for running the flow cytometry analysis and A Goldreich for typing the manuscript. This work was supported by a grant from the Israel Academy Science Foundation.

    Funding

    We thank U Caro for running the flow cytometry analysis and A Goldreich for typing the manuscript. This work was supported by a grant from the Israel Academy Science Foundation.

    FundersFunder number
    Israel Academy Science Foundation

      Keywords

      • Ionizing-radiation
      • Nuclear
      • T cell
      • Tyrosine kinase
      • p94(fer)

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