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SHIP,细胞因子诱导信号传导中的新成员。

SHIP, a new player in cytokine-induced signalling.

作者信息

Liu L, Damen J E, Ware M, Hughes M, Krystal G

机构信息

Terry Fox Laboratory, British Columbia Cancer Research Centre, Vancouver, Canada.

出版信息

Leukemia. 1997 Feb;11(2):181-4. doi: 10.1038/sj.leu.2400559.

DOI:10.1038/sj.leu.2400559
PMID:9009077
Abstract

We recently purified and cloned the cDNAs for the murine and human forms of a novel 145 kDa inositol polyphosphate 5-phosphatase (5-ptase) that becomes tyrosine phosphorylated and associated with Shc following stimulation of hemopoietic cells with multiple cytokines. Unlike most 5-ptases which hydrolyze phosphatidylinositol-4,5-P2-bisphosphate (PI-4,5-P2) and/or inositol-1,4,5-trisphosphate (I-1,4,5-P3), this enzyme selectively hydrolyzes the 5'-phosphate from inositol-1,3,4,5-tetraphosphate (I-1,3,4,5-P4) and phosphatidylinositol-3,4,5-trisphosphate (PI-3,4,5-P3), two inositol polyphosphates recently implicated in growth factor-mediated signalling. This 5-ptase is also unique among 5-ptases in that it is the only one to date to possess an SH2 domain. In this review we discuss the cloning, the Shc binding and the potential role of this protein, which we call SHIP, for SH2-containing inositol 5-phosphatase, in cell proliferation, differentiation and apoptosis.

摘要

我们最近纯化并克隆了小鼠和人类新型145 kDa肌醇多磷酸5-磷酸酶(5-ptase)的cDNA,该酶在多种细胞因子刺激造血细胞后会发生酪氨酸磷酸化并与Shc结合。与大多数水解磷脂酰肌醇-4,5-二磷酸(PI-4,5-P2)和/或肌醇-1,4,5-三磷酸(I-1,4,5-P3)的5-ptase不同,这种酶选择性地从肌醇-1,3,4,5-四磷酸(I-1,3,4,5-P4)和磷脂酰肌醇-3,4,5-三磷酸(PI-3,4,5-P3)中水解5'-磷酸,这两种肌醇多磷酸最近被认为与生长因子介导的信号传导有关。这种5-ptase在5-ptase中也是独特的,因为它是迄今为止唯一拥有SH2结构域的。在这篇综述中,我们讨论了这种我们称为SHIP(含SH2结构域的肌醇5-磷酸酶)的蛋白质的克隆、与Shc的结合及其在细胞增殖、分化和凋亡中的潜在作用。

相似文献

1
SHIP, a new player in cytokine-induced signalling.SHIP,细胞因子诱导信号传导中的新成员。
Leukemia. 1997 Feb;11(2):181-4. doi: 10.1038/sj.leu.2400559.
2
The 145-kDa protein induced to associate with Shc by multiple cytokines is an inositol tetraphosphate and phosphatidylinositol 3,4,5-triphosphate 5-phosphatase.由多种细胞因子诱导与Shc结合的145 kDa蛋白是一种肌醇四磷酸和磷脂酰肌醇3,4,5-三磷酸5-磷酸酶。
Proc Natl Acad Sci U S A. 1996 Feb 20;93(4):1689-93. doi: 10.1073/pnas.93.4.1689.
3
Purification and molecular cloning of SH2- and SH3-containing inositol polyphosphate-5-phosphatase, which is involved in the signaling pathway of granulocyte-macrophage colony-stimulating factor, erythropoietin, and Bcr-Abl.含SH2和SH3结构域的肌醇多磷酸-5-磷酸酶的纯化及分子克隆,该酶参与粒细胞-巨噬细胞集落刺激因子、促红细胞生成素和Bcr-Abl的信号通路。
Blood. 1997 Apr 15;89(8):2745-56.
4
p150Ship, a signal transduction molecule with inositol polyphosphate-5-phosphatase activity.p150Ship,一种具有肌醇多磷酸-5-磷酸酶活性的信号转导分子。
Genes Dev. 1996 May 1;10(9):1084-95. doi: 10.1101/gad.10.9.1084.
5
Role of the Src homology 2 (SH2) domain and C-terminus tyrosine phosphorylation sites of SH2-containing inositol phosphatase (SHIP) in the regulation of insulin-induced mitogenesis.含Src同源2(SH2)结构域的肌醇磷酸酶(SHIP)的SH2结构域和C末端酪氨酸磷酸化位点在胰岛素诱导的有丝分裂调控中的作用。
Endocrinology. 1999 Oct;140(10):4585-94. doi: 10.1210/endo.140.10.7028.
6
Multiple forms of an inositol polyphosphate 5-phosphatase form signaling complexes with Shc and Grb2.一种肌醇多磷酸5-磷酸酶的多种形式与Shc和Grb2形成信号复合物。
Curr Biol. 1996 Apr 1;6(4):438-45. doi: 10.1016/s0960-9822(02)00511-0.
7
Tyrosine phosphorylation of shc in response to B cell antigen receptor engagement depends on the SHIP inositol phosphatase.响应B细胞抗原受体结合时,shc的酪氨酸磷酸化依赖于SHIP肌醇磷酸酶。
J Immunol. 1999 Dec 1;163(11):5891-5.
8
Cloning and characterization of human SHIP, the 145-kD inositol 5-phosphatase that associates with SHC after cytokine stimulation.人SHIP的克隆与特性分析,SHIP是一种145kD的肌醇5-磷酸酶,在细胞因子刺激后与SHC结合。
Blood. 1996 Oct 15;88(8):2833-40.
9
Flt3 signaling involves tyrosyl-phosphorylation of SHP-2 and SHIP and their association with Grb2 and Shc in Baf3/Flt3 cells.Flt3信号传导涉及SHP-2和SHIP的酪氨酸磷酸化及其在Baf3/Flt3细胞中与Grb2和Shc的结合。
J Leukoc Biol. 1999 Mar;65(3):372-80. doi: 10.1002/jlb.65.3.372.
10
Protein interactions of Src homology 2 (SH2) domain-containing inositol phosphatase (SHIP): association with Shc displaces SHIP from FcgammaRIIb in B cells.含Src同源2(SH2)结构域的肌醇磷酸酶(SHIP)的蛋白质相互作用:与Shc的结合使SHIP从B细胞中的FcγRIIb上解离下来。
J Immunol. 1999 Feb 1;162(3):1408-14.

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Murine pancreatic adenocarcinoma dampens SHIP-1 expression and alters MDSC homeostasis and function.鼠胰腺腺癌降低 SHIP-1 的表达,并改变髓系来源抑制细胞的体内平衡和功能。
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SHIP1 inhibition increases immunoregulatory capacity and triggers apoptosis of hematopoietic cancer cells.SHIP1 抑制作用可增强免疫调节能力,并触发造血系统癌细胞凋亡。
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