• 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

Nuclear matrix proteins specific for subtypes of human hematopoietic cells.

作者信息

Gerner C, Sauermann G

机构信息

Institute of Tumor Biology-Cancer Research, University of Vienna, Austria.

出版信息

J Cell Biochem. 1999 Mar 15;72(4):470-82.

PMID:10022607
Abstract

Nuclear matrices were prepared from isolated subtypes of human hematopoietic cells and from cultured leukemia cells. The nuclear matrix proteins were analyzed by high-resolution two-dimensional gel electrophoresis and computer-assisted image analysis. While more than 200 protein spots were shared among the cells, about 50 distinct spots were found characteristic for individual cells or groups of related cells. This allowed to differentiate between hematopoietic cells and nonhematopoietic cells, lymphocytes and myeloid cells, monocytes, neutrophils, and promyelocytic leukemia cells. B and T lymphocytes could not be differentiated. Myeloid cells with their polymorph nuclei were characterized by the presence of 13 and by the absence of seven distinct spots, as well as by low concentrations of nuclear lamins and of heterogeneous nuclear ribonucleoproteins. Neutrophils with multilobular nuclei displayed six additional spots, while lacking 18 nuclear matrix protein spots. The nuclear matrix of proliferating cells showed three distinct spots in addition to proliferating cell nuclear antigen, increased concentrations of numatrin (B23), and heterogeneous nuclear ribonucleoproteins. The described cell-specific nuclear matrix proteins may represent new markers for hematopoietic cells.

摘要

相似文献

1
Nuclear matrix proteins specific for subtypes of human hematopoietic cells.
J Cell Biochem. 1999 Mar 15;72(4):470-82.
2
Proteomic analysis of the nuclear matrix in the early stages of rat liver carcinogenesis: identification of differentially expressed and MAR-binding proteins.大鼠肝癌发生早期核基质的蛋白质组学分析:差异表达及MAR结合蛋白的鉴定
Exp Cell Res. 2009 Jan 15;315(2):226-39. doi: 10.1016/j.yexcr.2008.10.017. Epub 2008 Oct 28.
3
Alteration of nuclear matrix protein composition during apoptosis in rat embryo cells.
Exp Cell Res. 1998 Feb 1;238(2):472-80. doi: 10.1006/excr.1997.3866.
4
Similarity between nuclear matrix proteins of various cells revealed by an improved isolation method.一种改进的分离方法揭示了不同细胞的核基质蛋白之间的相似性。
J Cell Biochem. 1998 Dec 1;71(3):363-74. doi: 10.1002/(sici)1097-4644(19981201)71:3<363::aid-jcb5>3.0.co;2-w.
5
Small heat shock protein p26 associates with nuclear lamins and HSP70 in nuclei and nuclear matrix fractions from stressed cells.小热休克蛋白p26在应激细胞的细胞核及核基质组分中,与核纤层蛋白和HSP70相结合。
J Cell Biochem. 2002;84(3):601-14.
6
Common nuclear matrix proteins in rat tissues.大鼠组织中常见的核基质蛋白。
Electrophoresis. 1997 Oct;18(11):2109-15. doi: 10.1002/elps.1150181138.
7
Proteomic analysis of nuclear matrix proteins during arsenic trioxide induced apoptosis in leukemia K562 cells.
Chin Med J (Engl). 2005 Jan 20;118(2):100-4.
8
In vitro heat exposure induces a redistribution of nuclear matrix proteins in human K562 erythroleukemia cells.体外热暴露诱导人K562红白血病细胞核基质蛋白重新分布。
Exp Cell Res. 1994 Jul;213(1):275-85. doi: 10.1006/excr.1994.1199.
9
Influence of different metal ions on the ultrastructure, biochemical properties, and protein localization of the K562 cell nuclear matrix.不同金属离子对K562细胞核基质的超微结构、生化特性及蛋白质定位的影响
J Cell Biochem. 1999 Jun 1;73(3):342-54.
10
Nuclear matrix of human ovarian cancer cells in vitro.体外培养的人卵巢癌细胞的核基质
Anticancer Res. 1998 Jul-Aug;18(4A):2535-9.

引用本文的文献

1
Transformation resistance in a premature aging disorder identifies a tumor-protective function of BRD4.早衰症中的转化抗性确定了BRD4的肿瘤保护功能。
Cell Rep. 2014 Oct 9;9(1):248-260. doi: 10.1016/j.celrep.2014.08.069. Epub 2014 Oct 2.
2
Label-free mass spectrometry exploits dozens of detected peptides to quantify lamins in wildtype and knockdown cells.无标记质谱利用数十种检测到的肽来定量野生型和敲低细胞中的核纤层蛋白。
Nucleus. 2013 Nov-Dec;4(6):450-9. doi: 10.4161/nucl.27413. Epub 2013 Dec 6.
3
Lamins regulate cell trafficking and lineage maturation of adult human hematopoietic cells.
核纤层蛋白调节成人人类造血细胞的细胞运输和谱系成熟。
Proc Natl Acad Sci U S A. 2013 Nov 19;110(47):18892-7. doi: 10.1073/pnas.1304996110. Epub 2013 Nov 4.
4
Proteome signatures of inflammatory activated primary human peripheral blood mononuclear cells.炎症激活的原代人外周血单个核细胞的蛋白质组学特征。
J Proteomics. 2012 Dec 5;76 Spec No.(5):150-62. doi: 10.1016/j.jprot.2012.07.012. Epub 2012 Jul 16.
5
Regulation of Metnase's TIR binding activity by its binding partner, Pso4.Metnase 的 TIR 结合活性受其结合伴侣 Pso4 的调节。
Arch Biochem Biophys. 2010 Jun 15;498(2):89-94. doi: 10.1016/j.abb.2010.04.011. Epub 2010 Apr 20.
6
Human Pso4 is a metnase (SETMAR)-binding partner that regulates metnase function in DNA repair.人类Pso4是一种与metnase(SETMAR)结合的蛋白,在DNA修复过程中调节metnase的功能。
J Biol Chem. 2008 Apr 4;283(14):9023-30. doi: 10.1074/jbc.M800150200. Epub 2008 Feb 8.