SOCS1 deficiency causes a lymphocyte-dependent perinatal lethality

被引:453
作者
Marine, JC
Topham, DJ
McKay, C
Wang, DM
Parganas, E
Stravopodis, D
Yoshimura, A
Ihle, JN
机构
[1] St Jude Childrens Res Hosp, Howard Hughes Med Inst, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Biochem, Memphis, TN 38105 USA
[3] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA
[4] Univ Tennessee, Sch Med, Dept Biochem, Memphis, TN USA
[5] Kurume Univ, Inst Life Sci, Kurume, Fukuoka 8390861, Japan
关键词
D O I
10.1016/S0092-8674(00)80048-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
SOCS1. is an SH2-containing protein that is primarily expressed in thymocytes in a cytokine- and T cell receptor-independent manner. SOCS1 deletion causes perinatal lethality with death by 2-3 weeks. During this period thymic changes include a loss of cellularity and a switch from predominantly CD4(+)CD8(+) to single positive cells. Peripheral T cells express activation antigens and proliferate to IL-2 in the absence of anti-CD3. In addition, IFN gamma is present in the serum. Reconstitution of the lymphoid lineage of JAK3-deficient mice with SOCS1-deficient stem cells recapitulates the lethality and T cell alterations. Introducing a RAG2 or IFN gamma deficiency eliminates lethality. The results demonstrate that lymphocytes are critical to SOCS1-associated perinatal lethality and implicate SOCS1 in lymphocyte differentiation or regulation.
引用
收藏
页码:609 / 616
页数:8
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