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

被引:370
作者
Starr, R
Metcalf, D
Elefanty, AG
Brysha, M
Willson, TA
Nicola, NA
Hilton, DJ
Alexander, WS
机构
[1] Walter Eliza Hall Inst. of Med. Res., Coop. Res. Ctr. Cell. Growth Factors, Post Office Royal Melbourne Hospital
关键词
D O I
10.1073/pnas.95.24.14395
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页码:14395 / 14399
页数:5
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