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SOCS1缺陷导致淋巴细胞依赖性围产期致死率。

SOCS1 deficiency causes a lymphocyte-dependent perinatal lethality.

作者信息

Marine J C, Topham D J, McKay C, Wang D, Parganas E, Stravopodis D, Yoshimura A, Ihle J N

机构信息

Howard Hughes Medical Institute, and Department of Biochemistry, St. Jude Children's Research Hospital, Memphis, Tennessee 38105, USA.

出版信息

Cell. 1999 Sep 3;98(5):609-16. doi: 10.1016/s0092-8674(00)80048-3.

Abstract

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, IFNgamma 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 IFNgamma deficiency eliminates lethality. The results demonstrate that lymphocytes are critical to SOCS1-associated perinatal lethality and implicate SOCS1 in lymphocyte differentiation or regulation.

摘要

细胞因子信号转导抑制因子1(SOCS1)是一种含Src同源2结构域(SH2)的蛋白质,主要以细胞因子和T细胞受体非依赖的方式在胸腺细胞中表达。SOCS1基因缺失会导致围产期致死,小鼠在2至3周龄时死亡。在此期间,胸腺变化包括细胞数量减少,以及从主要为CD4+CD8+双阳性细胞向单阳性细胞的转变。外周T细胞表达活化抗原,并且在没有抗CD3的情况下对白细胞介素-2(IL-2)产生增殖反应。此外,血清中存在γ干扰素(IFNγ)。用SOCS1基因缺陷的干细胞重建JAK3基因缺陷小鼠的淋巴谱系,可重现致死性和T细胞改变。引入重组激活基因2(RAG2)缺陷或IFNγ缺陷可消除致死性。这些结果表明,淋巴细胞对SOCS1相关的围产期致死至关重要,并提示SOCS1参与淋巴细胞分化或调节。

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