• 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

关于CR2阳性的伯基特淋巴瘤衍生细胞系(拉吉细胞系)上存在C3(溶血无活性)、C3b和C3d的三个结合位点的证据。

Evidence for three binding sites for C3 (hemolytically inactive), C3b and C3d on a CR2-positive Burkitt lymphoma-derived cell line (Raji).

作者信息

Barile G, Di Renzo L, Lipari M, Frati L, Faggioni A

机构信息

Istituto Tecnologie Biomediche, CNR, Rome, Italy.

出版信息

FEBS Lett. 1993 Jun 21;324(3):319-24. doi: 10.1016/0014-5793(93)80143-i.

DOI:10.1016/0014-5793(93)80143-i
PMID:8405374
Abstract

The present investigation shows that C3 (hemolytic inactive) as well as C3b and C3d bind Raji, a CR2-positive Burkitt lymphoma-derived cell line. Pretreatment of the cells with OKB-7 inhibited the binding of C3, whereas pretreatment with HB-5 inhibited the binding of C3b. Furthermore, the cells coated either with OKB-7 or HB-5 bound high amounts of C3d. TPA-treated cells showed binding for C3b and weak binding for C3 and C3d. Taken together, the data suggest that Raji cells may express three binding sites for C3, C3b and C3d which can be differently modulated by anti-CR2 MoAbs and TPA.

摘要

目前的研究表明,C3(溶血无活性)以及C3b和C3d可结合Raji细胞,这是一种源自CR2阳性伯基特淋巴瘤的细胞系。用OKB-7预处理细胞可抑制C3的结合,而用HB-5预处理则可抑制C3b的结合。此外,用OKB-7或HB-5包被的细胞可结合大量C3d。经佛波酯(TPA)处理的细胞显示出对C3b的结合以及对C3和C3d的弱结合。综上所述,数据表明Raji细胞可能表达C3、C3b和C3d的三个结合位点,这些位点可被抗CR2单克隆抗体和TPA以不同方式调节。

相似文献

1
Evidence for three binding sites for C3 (hemolytically inactive), C3b and C3d on a CR2-positive Burkitt lymphoma-derived cell line (Raji).关于CR2阳性的伯基特淋巴瘤衍生细胞系(拉吉细胞系)上存在C3(溶血无活性)、C3b和C3d的三个结合位点的证据。
FEBS Lett. 1993 Jun 21;324(3):319-24. doi: 10.1016/0014-5793(93)80143-i.
2
Analysis of C3b/C3d binding sites and factor I cofactor regions within mouse complement receptors 1 and 2.小鼠补体受体1和2内C3b/C3d结合位点及I因子辅助因子区域的分析
J Immunol. 1994 Jul 15;153(2):789-95.
3
Histochemical contributions to the binding mechanism of complement (CR1, CR2) receptors.补体(CR1、CR2)受体结合机制的组织化学研究进展。
Pathol Oncol Res. 2009 Dec;15(4):639-44. doi: 10.1007/s12253-009-9164-y. Epub 2009 Apr 8.
4
Neutrophils express a receptor for iC3b, C3dg, and C3d that is distinct from CR1, CR2, and CR3.中性粒细胞表达一种与CR1、CR2和CR3不同的iC3b、C3dg和C3d受体。
J Immunol. 1985 Apr;134(4):2571-9.
5
Ligand specificities of mouse complement receptor types 1 (CR1) and 2 (CR2) purified from spleen cells.
Int Immunol. 1993 Apr;5(4):337-43. doi: 10.1093/intimm/5.4.337.
6
Evidence for multiple sites of interaction in C3 for complement receptor type 2 (C3d/EBV receptor, CD21).补体受体2(C3d/EB病毒受体,CD21)在C3中多个相互作用位点的证据。
Eur J Immunol. 1991 Nov;21(11):2829-38. doi: 10.1002/eji.1830211126.
7
A comparative evaluation of receptor reactivities for C3b, iC3b, and C3d on Raji lymphoblastoid cells.对Raji淋巴母细胞上C3b、iC3b和C3d受体反应性的比较评估。
Int Arch Allergy Appl Immunol. 1982;69(3):231-7. doi: 10.1159/000233176.
8
Generation of three different fragments of bound C3 with purified factor I or serum. II. Location of binding sites in the C3 fragments for factors B and H, complement receptors, and bovine conglutinin.用纯化的I因子或血清生成结合C3的三种不同片段。II. C3片段中B因子、H因子、补体受体和牛胶固素结合位点的定位。
J Exp Med. 1983 Aug 1;158(2):334-52. doi: 10.1084/jem.158.2.334.
9
Studies of the Epstein Barr virus receptor found on Raji cells. II. A comparison of lymphocyte binding sites for Epstein Barr virus and C3d.对拉吉细胞上发现的爱泼斯坦-巴尔病毒受体的研究。II. 爱泼斯坦-巴尔病毒和C3d的淋巴细胞结合位点比较。
J Immunol. 1983 Mar;130(3):1309-12.
10
Identification of a 145,000 Mr membrane protein as the C3d receptor (CR2) of human B lymphocytes.鉴定一种145,000道尔顿的膜蛋白为人B淋巴细胞的C3d受体(CR2)。
Proc Natl Acad Sci U S A. 1984 Feb;81(3):881-5. doi: 10.1073/pnas.81.3.881.

引用本文的文献

1
The fixation of complement protein pairs to CR2 isoforms.补体蛋白对与CR2亚型的结合。
Biochem Biophys Rep. 2024 Feb 10;38:101657. doi: 10.1016/j.bbrep.2024.101657. eCollection 2024 Jul.
2
Co-operation between human CR1 (CD35) and CR2 (CD21) in internalization of their C3b and iC3b ligands by murine-transfected fibroblasts.人CR1(CD35)与CR2(CD21)在鼠转染成纤维细胞内化其C3b和iC3b配体过程中的合作。
Immunology. 1999 Sep;98(1):152-7. doi: 10.1046/j.1365-2567.1999.00839.x.
3
The requirement of localized, CR2-mediated, alternative pathway activation of complement for covalent deposition of C3 fragments on normal B cells.
补体C3片段在正常B细胞上共价沉积需要局部的、由CR2介导的补体替代途径激活。
Immunology. 1998 Feb;93(2):177-83. doi: 10.1046/j.1365-2567.1998.00429.x.