Liver degeneration and lymphoid deficiencies in mice lacking suppressor of cytokine signaling-1

  1. Robyn Starr,
  2. Donald Metcalf,
  3. Andrew G. Elefanty,
  4. Marta Brysha,
  5. Tracy A. Willson,
  6. Nicos A. Nicola,
  7. Douglas J. Hilton, and
  8. Warren S. Alexander*
  1. Walter and Eliza Hall Institute of Medical Research and Cooperative Research Centre for Cellular Growth Factors, Post Office Royal Melbourne Hospital, Victoria 3050, Australia
  1. Contributed by Donald Metcalf

Abstract

SOCS-1, a member of the suppressor of cytokine signaling (SOCS) family, was identified in a genetic screen for inhibitors of interleukin 6 signal transduction. SOCS-1 transcription is induced by cytokines, and the protein binds and inhibits Janus kinases and reduces cytokine-stimulated tyrosine phosphorylation of signal transducers and activators of transcription 3 and the gp130 component of the interleukin 6 receptor. Thus, SOCS-1 forms part of a feedback loop that modulates signal transduction from cytokine receptors. To examine the role of SOCS-1 in vivo, we have used gene targeting to generate mice lacking this protein. SOCS-1−/− mice exhibited stunted growth and died before weaning with fatty degeneration of the liver and monocytic infiltration of several organs. In addition, the thymus of SOCS-1−/− mice was reduced markedly in size, and there was a progressive loss of maturing B lymphocytes in the bone marrow, spleen, and peripheral blood. Thus, SOCS-1 is required for in vivo regulation of multiple cell types and is indispensable for normal postnatal growth and survival.

Footnotes

  • * To whom reprint requests should be addressed. e-mail: alexander_w{at}wehi.edu.au.

  • ABBREVIATIONS:
    SOCS,
    suppressor of cytokine signaling;
    STAT,
    signal transducers and activators of transcription;
    IL,
    interleukin;
    kb,
    kilobase;
    ES,
    embryonic stem
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