肿瘤抑制因子
信号转导
糖蛋白130
细胞因子
生物
细胞因子受体
普通伽马链
受体
细胞生物学
Janus激酶1
白细胞介素12受体,β1亚单位
白细胞介素-6受体
JAK-STAT信号通路
白细胞介素-21受体
免疫学
白细胞介素
白细胞介素6
白细胞介素10
贾纳斯激酶
遗传学
受体酪氨酸激酶
标识
DOI:10.1016/j.cytogfr.2015.07.006
摘要
Oncostatin M (OSM) and interleukin-31 (IL-31) are two cytokines belonging to the IL-6 family which share a common signaling receptor subunit, the OSM receptor beta (OSMRβ). Both of them are released by monocytes/macrophages, dendritic cells and T lymphocytes in inflammatory situations and upon binding to their respective receptor complexes they signal mainly via the JAK/STAT pathway. Besides sharing many biochemical properties, both display divergent physiological functions. This review summarizes aspects of cytokine transcription and biosynthesis, cytokine–receptor interactions, cross-species activities, signal transduction and physiology delineated from recent findings in genetic mouse models for both cytokines, OSM and IL-31.
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