Liver degeneration and lymphoid deficiencies in mice lacking suppressor of cytokine signaling-1
- Robyn Starr,
- Donald Metcalf,
- Andrew G. Elefanty,
- Marta Brysha,
- Tracy A. Willson,
- Nicos A. Nicola,
- Douglas J. Hilton, and
- Warren S. Alexander*
- Walter and Eliza Hall Institute of Medical Research and Cooperative Research Centre for Cellular Growth Factors, Post Office Royal Melbourne Hospital, Victoria 3050, Australia
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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
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↵ * 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
- Copyright © 1998, The National Academy of Sciences








