肿瘤抑制因子
糖蛋白130
白血病抑制因子
白细胞介素10受体,α亚单位
受体
分子生物学
白细胞介素-21受体
细胞因子受体
白细胞介素5受体α亚单位
化学
白细胞介素12受体,β1亚单位
蛋白质亚单位
生物
生物化学
Gα亚单位
信号转导
细胞因子
白细胞介素6
免疫学
胚胎干细胞
车站3
基因
作者
David P. Gearing,Michael R. Comeau,Della Friend,Steven D. Gimpel,Catherine J. Thut,Jackie McGourty,Kelle K. Brasher,Julie A. King,Steven Gillis,Bruce Mosley,Steven F. Ziegler,David Cosman
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1992-03-13
卷期号:255 (5050): 1434-1437
被引量:897
标识
DOI:10.1126/science.1542794
摘要
Leukemia inhibitory factor (LIF) and interleukin-6 (IL-6) are multifunctional cytokines with many similar activities. LIF is structurally and functionally related to another cytokine, Oncostatin M (OSM), that binds to the high-affinity LIF receptor but not to the low-affinity LIF receptor. A complementary DNA was isolated that encodes the high-affinity converting subunit of the LIF receptor. The converter conferred high-affinity binding of both LIF and OSM when expressed with the low-affinity LIF receptor and is identical to the signal transducing subunit of the IL-6 receptor, gp130. The gp130 subunit alone confers low-affinity binding of OSM when expressed in COS-7 cells. This receptor system resembles the high-affinity receptors for granulocyte-macrophage colony-stimulating factor, IL-3, and IL-5, which share a common subunit.
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