• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

CD45 酪氨酸蛋白磷酸酶表达对 lck、fyn 和 c-src 酪氨酸蛋白激酶酪氨酸磷酸化的差异影响。

Differential effects of expression of the CD45 tyrosine protein phosphatase on the tyrosine phosphorylation of the lck, fyn, and c-src tyrosine protein kinases.

作者信息

Hurley T R, Hyman R, Sefton B M

机构信息

Molecular Biology and Virology Laboratory, Salk Institute, San Diego, California 92186.

出版信息

Mol Cell Biol. 1993 Mar;13(3):1651-6. doi: 10.1128/mcb.13.3.1651-1656.1993.

DOI:10.1128/mcb.13.3.1651-1656.1993
PMID:8441403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC359477/
Abstract

Expression of the CD45 tyrosine protein phosphatase is required for the response of functional lymphocytes to stimulation through the antigen receptor. One or more of its substrates may therefore be essential for signal transduction during lymphocyte activation. We have studied the phosphorylation of the closely related lck, fyn, and c-src tyrosine protein kinases in leukemic murine T-cell lines that have lost the expression of CD45. The phosphorylation of the lck kinase at an inhibitory site of tyrosine phosphorylation, Tyr-505, was increased by two-, six-, and eightfold in three different cell lines. Phosphorylation of the fyn kinase at the homologous site, Tyr-531, was unaltered in one of these cell lines, but increased by 2.5-fold in the two others. The phosphorylation of p60c-src at the homologous tyrosine was essentially unchanged in the one CD45-negative cell line in which it was examined. The expression of CD45 therefore regulates the phosphorylation and potentially the activity of the lck and fyn tyrosine protein kinases, but the effect on the lck kinase is much greater than on the fyn kinase. This finding and the observation that CD45 had no effect on the phosphorylation of p60c-src suggest that CD45 exhibits polypeptide substrate specificity in vivo. Additionally, these findings are consistent with the hypothesis that the unresponsiveness of CD45-negative lymphoid cells to antigenic stimulation is due largely to hyperphosphorylation of the lck kinase.

摘要

功能性淋巴细胞通过抗原受体对刺激作出反应需要CD45酪氨酸蛋白磷酸酶的表达。因此,其一种或多种底物可能是淋巴细胞活化过程中信号转导所必需的。我们研究了在已丧失CD45表达的白血病小鼠T细胞系中,密切相关的lck、fyn和c-src酪氨酸蛋白激酶的磷酸化情况。在三种不同的细胞系中,lck激酶在酪氨酸磷酸化抑制位点Tyr-505处的磷酸化增加了2倍、6倍和8倍。fyn激酶在同源位点Tyr-531处的磷酸化在其中一个细胞系中未改变,但在另外两个细胞系中增加了2.5倍。在所检测的一个CD45阴性细胞系中,p60c-src在同源酪氨酸处的磷酸化基本未变。因此,CD45的表达调节lck和fyn酪氨酸蛋白激酶的磷酸化以及潜在的活性,但对lck激酶的影响远大于对fyn激酶的影响。这一发现以及CD45对p60c-src磷酸化无影响的观察结果表明,CD45在体内表现出多肽底物特异性。此外,这些发现与以下假设一致,即CD45阴性淋巴细胞对抗抗原刺激无反应主要是由于lck激酶的过度磷酸化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/41a7fb6e8252/molcellb00015-0352-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/db0f313ee41d/molcellb00015-0351-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/5485db0955cc/molcellb00015-0351-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/bc418e36d7f2/molcellb00015-0352-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/41a7fb6e8252/molcellb00015-0352-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/db0f313ee41d/molcellb00015-0351-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/5485db0955cc/molcellb00015-0351-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/bc418e36d7f2/molcellb00015-0352-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61fb/359477/41a7fb6e8252/molcellb00015-0352-b.jpg

相似文献

1
Differential effects of expression of the CD45 tyrosine protein phosphatase on the tyrosine phosphorylation of the lck, fyn, and c-src tyrosine protein kinases.CD45 酪氨酸蛋白磷酸酶表达对 lck、fyn 和 c-src 酪氨酸蛋白激酶酪氨酸磷酸化的差异影响。
Mol Cell Biol. 1993 Mar;13(3):1651-6. doi: 10.1128/mcb.13.3.1651-1656.1993.
2
Correlation between Src family member regulation by the protein-tyrosine-phosphatase CD45 and transmembrane signaling through the T-cell receptor.蛋白酪氨酸磷酸酶CD45对Src家族成员的调控与通过T细胞受体的跨膜信号传导之间的相关性。
Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1402-6. doi: 10.1073/pnas.90.4.1402.
3
CD45 regulation of tyrosine phosphorylation and enzyme activity of src family kinases.CD45对src家族激酶酪氨酸磷酸化和酶活性的调节。
J Biol Chem. 1994 May 6;269(18):13594-600.
4
Mutational analysis of Lck in CD45-negative T cells: dominant role of tyrosine 394 phosphorylation in kinase activity.CD45 阴性 T 细胞中 Lck 的突变分析:酪氨酸 394 磷酸化在激酶活性中的主导作用
Mol Cell Biol. 1996 Sep;16(9):4996-5003. doi: 10.1128/MCB.16.9.4996.
5
CD45 and RPTPalpha display different protein tyrosine phosphatase activities in T lymphocytes.CD45和RPTPα在T淋巴细胞中表现出不同的蛋白酪氨酸磷酸酶活性。
Biochem J. 1997 Nov 1;327 ( Pt 3)(Pt 3):867-76. doi: 10.1042/bj3270867.
6
Tyrosine phosphorylation of CD45 phosphotyrosine phosphatase by p50csk kinase creates a binding site for p56lck tyrosine kinase and activates the phosphatase.p50csk激酶对CD45磷酸酪氨酸磷酸酶进行酪氨酸磷酸化,为p56lck酪氨酸激酶创造一个结合位点并激活该磷酸酶。
Mol Cell Biol. 1994 Feb;14(2):1308-21. doi: 10.1128/mcb.14.2.1308-1321.1994.
7
Regulation of Ly49D/DAP12 signal transduction by Src-family kinases and CD45.Src家族激酶和CD45对Ly49D/DAP12信号转导的调控
J Immunol. 2006 Jun 1;176(11):6615-23. doi: 10.4049/jimmunol.176.11.6615.
8
Regulation of Lck and Fyn tyrosine kinase activities by transmembrane protein tyrosine phosphatase leukocyte common antigen-related molecule.跨膜蛋白酪氨酸磷酸酶白细胞共同抗原相关分子对Lck和Fyn酪氨酸激酶活性的调节
Mol Cancer Res. 2002 Dec;1(2):155-63.
9
CD44-initiated cell spreading induces Pyk2 phosphorylation, is mediated by Src family kinases, and is negatively regulated by CD45.CD44启动的细胞铺展诱导Pyk2磷酸化,由Src家族激酶介导,并受CD45负调控。
J Biol Chem. 2001 Aug 3;276(31):28767-73. doi: 10.1074/jbc.M100158200. Epub 2001 May 21.
10
Increase in the specific activity of p50csk in proliferating T cells correlates with decreased specific activity of p56lck and p59fyn and reduced phosphorylation of CD3 subunits.增殖性T细胞中p50csk的比活性增加与p56lck和p59fyn的比活性降低以及CD3亚基磷酸化减少相关。
Mol Immunol. 1996 Apr;33(6):531-40. doi: 10.1016/0161-5890(96)00006-5.

引用本文的文献

1
Sensitive FRET Biosensor Reveals Fyn Kinase Regulation by Submembrane Localization.敏感的 FRET 生物传感器揭示了 Fyn 激酶通过亚膜定位的调节。
ACS Sens. 2019 Jan 25;4(1):76-86. doi: 10.1021/acssensors.8b00896. Epub 2019 Jan 9.
2
Cluster of differentiation 45 activation is crucial in interleukin-10-dependent tumor-associated dendritic cell differentiation.分化簇45的激活在白细胞介素-10依赖性肿瘤相关树突状细胞分化中至关重要。
Oncol Lett. 2014 Aug;8(2):620-626. doi: 10.3892/ol.2014.2161. Epub 2014 May 19.
3
Regulation of TCR signalling by tyrosine phosphatases: from immune homeostasis to autoimmunity.

本文引用的文献

1
Two complementation classes of T200 (Ly-5) glycoprotein-negative mutants.T200(Ly-5)糖蛋白阴性突变体的两个互补类群。
Immunogenetics. 1981 Mar 1;12(5-6):511-23. doi: 10.1007/BF01561692.
2
Temperature-sensitive transformation by Rous sarcoma virus and temperature-sensitive protein kinase activity.劳氏肉瘤病毒的温度敏感型转化与温度敏感型蛋白激酶活性
J Virol. 1980 Jan;33(1):220-9. doi: 10.1128/JVI.33.1.220-229.1980.
3
A new technique for the assay of infectivity of human adenovirus 5 DNA.一种检测人腺病毒5型DNA感染性的新技术。
酪氨酸磷酸酶对 TCR 信号的调节:从免疫稳态到自身免疫。
Immunology. 2012 Sep;137(1):1-19. doi: 10.1111/j.1365-2567.2012.03591.x.
4
Lck, Membrane Microdomains, and TCR Triggering Machinery: Defining the New Rules of Engagement.Lck、膜微区和 TCR 触发机制:定义新的互动规则。
Front Immunol. 2012 Jun 12;3:155. doi: 10.3389/fimmu.2012.00155. eCollection 2012.
5
Loss of tyrosine phosphatase-dependent inhibition promotes activation of tyrosine kinase c-Src in detached pancreatic cells.脱离的胰腺细胞中酪氨酸磷酸酶依赖性抑制作用的丧失促进了酪氨酸激酶 c-Src 的激活。
Mol Carcinog. 2010 Dec;49(12):1007-21. doi: 10.1002/mc.20684.
6
Intracellular reactive oxygen species activate Src tyrosine kinase during cell adhesion and anchorage-dependent cell growth.细胞内活性氧在细胞黏附及锚定依赖性细胞生长过程中激活Src酪氨酸激酶。
Mol Cell Biol. 2005 Aug;25(15):6391-403. doi: 10.1128/MCB.25.15.6391-6403.2005.
7
T cell receptor engagement leads to phosphorylation of clathrin heavy chain during receptor internalization.T细胞受体结合导致受体内化过程中网格蛋白重链的磷酸化。
J Exp Med. 2004 Apr 5;199(7):981-91. doi: 10.1084/jem.20031105.
8
HIV-1 infection is facilitated in T cells by decreasing p56lck protein tyrosine kinase activity.通过降低p56lck蛋白酪氨酸激酶活性,HIV-1感染在T细胞中得以促进。
Clin Exp Immunol. 2003 Jul;133(1):78-90. doi: 10.1046/j.1365-2249.2003.02187.x.
9
Positive and negative regulation of T-cell activation through kinases and phosphatases.通过激酶和磷酸酶对T细胞活化的正负调控。
Biochem J. 2003 Apr 1;371(Pt 1):15-27. doi: 10.1042/BJ20021637.
10
Development of T-leukaemias in CD45 tyrosine phosphatase-deficient mutant lck mice.CD45酪氨酸磷酸酶缺陷型lck小鼠中T细胞白血病的发生
EMBO J. 2000 Sep 1;19(17):4644-54. doi: 10.1093/emboj/19.17.4644.
Virology. 1973 Apr;52(2):456-67. doi: 10.1016/0042-6822(73)90341-3.
4
Mutation of a site of tyrosine phosphorylation in the lymphocyte-specific tyrosine protein kinase, p56lck, reveals its oncogenic potential in fibroblasts.淋巴细胞特异性酪氨酸蛋白激酶p56lck中一个酪氨酸磷酸化位点的突变揭示了其在成纤维细胞中的致癌潜力。
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4247-51. doi: 10.1073/pnas.85.12.4247.
5
Neoplastic transformation induced by an activated lymphocyte-specific protein tyrosine kinase (pp56lck).由活化的淋巴细胞特异性蛋白酪氨酸激酶(pp56lck)诱导的肿瘤转化。
Mol Cell Biol. 1988 Feb;8(2):540-50. doi: 10.1128/mcb.8.2.540-550.1988.
6
The CD4 and CD8 T cell surface antigens are associated with the internal membrane tyrosine-protein kinase p56lck.CD4和CD8 T细胞表面抗原与内膜酪氨酸蛋白激酶p56lck相关。
Cell. 1988 Oct 21;55(2):301-8. doi: 10.1016/0092-8674(88)90053-0.
7
Post-translational alterations of the tyrosine kinase p56lck in response to activators of protein kinase C.酪氨酸激酶p56lck响应蛋白激酶C激活剂的翻译后改变
Oncogene Res. 1988 May;2(4):385-401.
8
T cell activation induces rapid tyrosine phosphorylation of a limited number of cellular substrates.T细胞活化诱导有限数量的细胞底物发生快速酪氨酸磷酸化。
J Biol Chem. 1989 Jun 25;264(18):10836-42.
9
Improved retroviral vectors for gene transfer and expression.用于基因转移和表达的改进型逆转录病毒载体。
Biotechniques. 1989 Oct;7(9):980-2, 984-6, 989-90.
10
Evidence that the leukocyte-common antigen is required for antigen-induced T lymphocyte proliferation.有证据表明,抗原诱导的T淋巴细胞增殖需要白细胞共同抗原。
Cell. 1989 Sep 22;58(6):1055-65. doi: 10.1016/0092-8674(89)90504-7.