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B细胞中的负向信号传导:SHIP、Grb和Shc

Negative signaling in B cells: SHIP Grbs Shc.

作者信息

Tridandapani S, Kelley T, Cooney D, Pradhan M, Coggeshall K M

机构信息

Ohio State University, Dept of Microbiology, Columbus 43210, USA.

出版信息

Immunol Today. 1997 Sep;18(9):424-7. doi: 10.1016/s0167-5699(97)01112-2.

DOI:10.1016/s0167-5699(97)01112-2
PMID:9293157
Abstract

Negative signaling in B cells is initiated by co-crosslinking of the antigen receptor and the Fcy receptor, resulting in cessation of B-cell signaling events and, in turn, inhibiting B-cell proliferation and antibody secretion. Here, a competitive role is proposed for SHIP in blocking the interaction of Shc with the Grb2-Sos complex of proteins that lead to Ras activation in B cells.

摘要

B细胞中的负向信号传导由抗原受体和Fcy受体的共交联引发,导致B细胞信号传导事件停止,进而抑制B细胞增殖和抗体分泌。在此,有人提出SHIP在阻断Shc与导致B细胞中Ras激活的蛋白质Grb2-Sos复合物相互作用方面具有竞争作用。

相似文献

1
Negative signaling in B cells: SHIP Grbs Shc.B细胞中的负向信号传导:SHIP、Grb和Shc
Immunol Today. 1997 Sep;18(9):424-7. doi: 10.1016/s0167-5699(97)01112-2.
2
Role of SHIP in FcgammaRIIb-mediated inhibition of Ras activation in B cells.SHIP在FcγRIIb介导的B细胞中Ras激活抑制作用中的角色。
Mol Immunol. 1998 Dec;35(17):1135-46. doi: 10.1016/s0161-5890(98)00097-2.
3
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.
4
The src homology domain 2-containing inositol phosphatase SHIP forms a ternary complex with Shc and Grb2 in antigen receptor-stimulated B lymphocytes.含src同源结构域2的肌醇磷酸酶SHIP在抗原受体刺激的B淋巴细胞中与Shc和Grb2形成三元复合物。
J Biol Chem. 1999 Apr 23;274(17):12183-91. doi: 10.1074/jbc.274.17.12183.
5
Activation-induced bi-dentate interaction of SHIP and Shc in B lymphocytes.SHIP与Shc在B淋巴细胞中的激活诱导双齿相互作用。
J Cell Biochem. 1997 Oct 1;67(1):32-42. doi: 10.1002/(sici)1097-4644(19971001)67:1<32::aid-jcb4>3.0.co;2-x.
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Mechanism of SHIP-mediated inhibition of insulin- and platelet-derived growth factor-stimulated mitogen-activated protein kinase activity in 3T3-L1 adipocytes.SHIP介导的对3T3-L1脂肪细胞中胰岛素和血小板衍生生长因子刺激的丝裂原活化蛋白激酶活性的抑制机制。
Mol Endocrinol. 2005 Feb;19(2):421-30. doi: 10.1210/me.2004-0096. Epub 2004 Oct 14.
7
Negative signaling in B lymphocytes induces tyrosine phosphorylation of the 145-kDa inositol polyphosphate 5-phosphatase, SHIP.B淋巴细胞中的负向信号传导可诱导145 kDa肌醇多磷酸5-磷酸酶SHIP发生酪氨酸磷酸化。
J Immunol. 1996 Sep 15;157(6):2234-8.
8
Inhibitory signaling by B cell Fc gamma RIIb.B细胞FcγRIIb的抑制性信号传导。
Curr Opin Immunol. 1998 Jun;10(3):306-12. doi: 10.1016/s0952-7915(98)80169-6.
9
Negative signaling in B cells causes reduced Ras activity by reducing Shc-Grb2 interactions.B细胞中的负向信号传导通过减少Shc-Grb2相互作用导致Ras活性降低。
J Immunol. 1997 Feb 1;158(3):1125-32.
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.

引用本文的文献

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FCRL1 Regulates B Cell Receptor-Induced ERK Activation through GRB2.FCRL1 通过 GRB2 调节 B 细胞受体诱导的 ERK 激活。
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Beyond the Cell Surface: Targeting Intracellular Negative Regulators to Enhance T cell Anti-Tumor Activity.超越细胞表面:靶向细胞内负调控因子以增强 T 细胞抗肿瘤活性。
Int J Mol Sci. 2019 Nov 20;20(23):5821. doi: 10.3390/ijms20235821.
3
Evidence for SH2 domain-containing 5'-inositol phosphatase-2 (SHIP2) contributing to a lymphatic dysfunction.
含SH2结构域的5'-肌醇磷酸酶-2(SHIP2)导致淋巴管功能障碍的证据。
PLoS One. 2014 Nov 10;9(11):e112548. doi: 10.1371/journal.pone.0112548. eCollection 2014.
4
T cell-specific deletion of the inositol phosphatase SHIP reveals its role in regulating Th1/Th2 and cytotoxic responses.T细胞特异性缺失肌醇磷酸酶SHIP揭示了其在调节Th1/Th2和细胞毒性反应中的作用。
Proc Natl Acad Sci U S A. 2007 Jul 3;104(27):11382-7. doi: 10.1073/pnas.0704853104. Epub 2007 Jun 21.
5
Macrophage pro-inflammatory response to Francisella novicida infection is regulated by SHIP.SHIP调节巨噬细胞对新凶手弗朗西斯菌感染的促炎反应。
PLoS Pathog. 2006 Jul;2(7):e71. doi: 10.1371/journal.ppat.0020071.
6
FcgammaR-induced production of superoxide and inflammatory cytokines is differentially regulated by SHIP through its influence on PI3K and/or Ras/Erk pathways.FcγR诱导的超氧化物和炎性细胞因子的产生通过SHIP对PI3K和/或Ras/Erk信号通路的影响而受到不同的调节。
Blood. 2006 Jul 15;108(2):718-25. doi: 10.1182/blood-2005-09-3889. Epub 2006 Mar 16.
7
Visualization of negative signaling in B cells by quantitative confocal microscopy.通过定量共聚焦显微镜观察B细胞中的负信号。
Mol Cell Biol. 2001 Dec;21(24):8615-25. doi: 10.1128/MCB.21.24.8615-8625.2001.
8
pp60c-src associates with the SH2-containing inositol-5-phosphatase SHIP1 and is involved in its tyrosine phosphorylation downstream of alphaIIbbeta3 integrin in human platelets.pp60c-src与含SH2结构域的肌醇-5-磷酸酶SHIP1相关联,并参与人血小板中αIIbβ3整合素下游SHIP1的酪氨酸磷酸化过程。
Biochem J. 2000 May 15;348 Pt 1(Pt 1):107-12.
9
Negative signaling in health and disease.健康与疾病中的负向信号传导。
Immunol Res. 1999;19(1):47-64. doi: 10.1007/BF02786476.
10
DSHP: a "power bar" for sustained immune responses?DSHP:持续免疫反应的“能量棒”?
Proc Natl Acad Sci U S A. 1998 Nov 10;95(23):13355-7. doi: 10.1073/pnas.95.23.13355.