状态4
斯达
生物
STAT6
转录因子
JAK-STAT信号通路
分子生物学
酪氨酸磷酸化
细胞生物学
白细胞介素4
信号转导
细胞因子
酪氨酸激酶
基因
免疫学
生物化学
车站3
作者
Jinzhao Hou,Ulrike Schindler,William J. Henzel,Tze Chun Ho,Mike Brasseur,Steven L. McKnight
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1994-09-16
卷期号:265 (5179): 1701-1706
被引量:856
标识
DOI:10.1126/science.8085155
摘要
Interleukin-4 (IL-4) is an immunomodulatory cytokine secreted by activated T lymphocytes, basophils, and mast cells. It plays an important role in modulating the balance of T helper (Th) cell subsets, favoring expansion of the Th2 lineage relative to Th1. Imbalance of these T lymphocyte subsets has been implicated in immunological diseases including allergy, inflammation, and autoimmune disease. IL-4 may mediate its biological effects, at least in part, by activating a tyrosine-phosphorylated DNA binding protein. This protein has now been purified and its encoding gene cloned. Examination of the primary amino acid sequence of this protein indicates that it is a member of the signal transducers and activators of transcription (Stat) family of DNA binding proteins, hereby designated IL-4 Stat. Study of the inhibitory activities of phosphotyrosine-containing peptides derived from the intracellular domain of the IL-4 receptor provided evidence for direct coupling of receptor and transcription factor during the IL-4 Stat activation cycle. Such observations indicate that IL-4 Stat has the same functional domain for both receptor coupling and dimerization.
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