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通过gp130的信号转导,这在白细胞介素6相关细胞因子亚家族的受体中是共享的。

Signal transduction through gp130 that is shared among the receptors for the interleukin 6 related cytokine subfamily.

作者信息

Hirano T, Matsuda T, Nakajima K

机构信息

Biomedical Research Center, Osaka University Medical School, Japan.

出版信息

Stem Cells. 1994 May;12(3):262-77. doi: 10.1002/stem.5530120303.

DOI:10.1002/stem.5530120303
PMID:8075593
Abstract

Interleukin 6 (IL-6) and related cytokines, such as leukemia inhibitory factor (LIF), oncostatin M (OSM), ciliary neurotrophic factor (CNTF) and IL-11 exhibit multiple functions and redundancy in biological activities and play important roles in the immune response, hematopoiesis, the nervous system and acute phase reactions. These IL-6 family cytokines exhibit a similar helical structure, and their receptors are structurally similar and constitute a cytokine receptor super family. In addition, a receptor subunit is shared among these IL-6 related cytokine subfamily receptors, contributing to one of the mechanisms of functional redundancy of cytokine activities and suggesting the presence of a common signal transduction pathway among these receptors. In this review, we describe the structure of the receptors for IL-6 and its related cytokine subfamily members. Furthermore, we propose a novel mechanism for the generation of cytokine diversity, i.e. the complex of a cytokine and one of its receptor subunits act as a novel cytokine on the cells that express the other receptor subunit(s) capable of acting as a receptor for the complex. Finally, we describe a Ras-independent novel signal transduction pathway that utilizes Jak tyrosine kinase family, Stat protein family and yet unidentified H-7-sensitive pathway. This signal transduction pathway is commonly generated through the receptors for a wide range of cytokines and growth factors.

摘要

白细胞介素6(IL-6)及相关细胞因子,如白血病抑制因子(LIF)、抑瘤素M(OSM)、睫状神经营养因子(CNTF)和IL-11,在生物活性方面具有多种功能且功能冗余,在免疫应答、造血作用、神经系统和急性期反应中发挥重要作用。这些IL-6家族细胞因子呈现相似的螺旋结构,其受体在结构上也相似,构成一个细胞因子受体超家族。此外,这些IL-6相关细胞因子亚家族受体共享一个受体亚基,这促成了细胞因子活性功能冗余的机制之一,并提示这些受体之间存在共同的信号转导途径。在本综述中,我们描述了IL-6及其相关细胞因子亚家族成员受体的结构。此外,我们提出了一种产生细胞因子多样性的新机制,即细胞因子与其一个受体亚基的复合物在表达能够作为该复合物受体的其他受体亚基的细胞上作为一种新的细胞因子发挥作用。最后,我们描述了一种不依赖Ras的新信号转导途径,该途径利用Jak酪氨酸激酶家族、Stat蛋白家族以及尚未明确的H-7敏感途径。这种信号转导途径通常通过多种细胞因子和生长因子的受体产生。

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