• 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

血小板无力症患者单核细胞上黏附结构Mo-1的正常表达。

Normal expression of the adhesive structure Mo-1 on monocytes from patients with Glanzmann's thrombasthenia.

作者信息

Setiadi H, Antoine C, Wautier J L

机构信息

Institut des Vaisseaux et du Sang (IVS) Hôpital Lariboisière, Paris.

出版信息

J Mal Vasc. 1991;16(1):30-1.

PMID:2010702
Abstract

The glycoprotein complex GPIIb-IIIa of the platelet membrane and CD18 of the monocyte membrane have been established as being the central figure for the adhesion processes of the corresponding cells. The molecular structure of these 2 GPs bears some similarities. It was proposed recently that LFA-1 and Mo-1 (CD18 family) and GPIIb-IIIa might be encoded by the same gene. For this purpose, we studied the expression of Mo-1, Mo-2 (as control) receptors on monocytes and GPIIIa and GPIIb-IIIa on platelets of two GT patients as compared to normal healthy subjects. Monoclonal antibodies anti Mo-1, MO-2, AP-3 and AP-2 were used to measure the expression of the respective antigens by indirect immunofluorescence procedure. The fluorescence of the labelled cells was analysed with an Ortho Cytofluorograph 50-H. The resulting Mean Fluorescence Intensity (MFI) values of AP-2 and AP-3 showed that the patients had a total absence of GPIIb-IIIa antigens. However, Mo-1, as well as those of control Mo-2, in patients (MO-1: 672 and 716; Mo-2: 453 and 637) were similar to that of normal subjects (Mo-1: 735 +/- 74; Mo-2: 585 +/- 35; mean +/- SEM). Therefore, the normal expression of Mo-1 receptors on the monocytes of Glanzmann's thrombasthenia patients suggests different genomic regulations for Mo-1 antigens on the monocyte and GPIIb-IIIa complex on the platelet.

摘要

血小板膜糖蛋白复合物GPIIb-IIIa和单核细胞膜CD18已被确认为相应细胞黏附过程的核心物质。这两种糖蛋白的分子结构有一些相似之处。最近有人提出,淋巴细胞功能相关抗原-1(LFA-1)和巨噬细胞抗原-1(Mo-1,CD18家族)以及GPIIb-IIIa可能由同一基因编码。为此,我们研究了两名血小板无力症(GT)患者与正常健康受试者相比,单核细胞上Mo-1、Mo-2(作为对照)受体以及血小板上GPIIIa和GPIIb-IIIa的表达情况。使用抗Mo-1、MO-2、AP-3和AP-2单克隆抗体,通过间接免疫荧光法测量各自抗原的表达。用Ortho Cytofluorograph 50-H分析标记细胞的荧光。AP-2和AP-3的平均荧光强度(MFI)值结果显示,患者完全缺乏GPIIb-IIIa抗原。然而,患者的Mo-1以及对照Mo-2的表达(Mo-1:672和716;Mo-2:453和637)与正常受试者相似(Mo-1:735±74;Mo-2:585±35;平均值±标准误)。因此,血小板无力症患者单核细胞上Mo-1受体的正常表达表明,单核细胞上的Mo-1抗原和血小板上的GPIIb-IIIa复合物存在不同的基因组调控。

相似文献

1
Normal expression of the adhesive structure Mo-1 on monocytes from patients with Glanzmann's thrombasthenia.血小板无力症患者单核细胞上黏附结构Mo-1的正常表达。
J Mal Vasc. 1991;16(1):30-1.
2
Glanzmann's thrombasthenia: updated.血小板无力症:最新进展。
Platelets. 2002 Nov;13(7):387-93. doi: 10.1080/0953710021000024394.
3
[Glanzmann's thrombasthenia: a rare example of an integrin deficit].[血小板无力症:整合素缺乏的罕见病例]
Recenti Prog Med. 1992 Oct;83(10):577-81.
4
No relationship in the expression of Mo-1 on monocytes and GP IIb-IIIa on platelets in Glanzmann's thrombasthenia.在Glanzmann血小板无力症中,单核细胞上的Mo-1表达与血小板上的糖蛋白IIb-IIIa表达之间无相关性。
Thromb Haemost. 1988 Apr 8;59(2):336.
5
Stimulated Glanzmann's thrombasthenia platelets produced microvesicles. Microvesiculation correlates better to exposure of procoagulant surface than to activation of GPIIb-IIIa.受刺激的血小板无力症血小板产生了微泡。微泡形成与促凝表面的暴露相关性更好,而非与糖蛋白IIb-IIIa的激活相关性更好。
Thromb Haemost. 1995 Dec;74(6):1533-40.
6
[Molecular pathology of inherited Glanzmann's thrombasthenia. Report of 11 cases].[遗传性血小板无力症的分子病理学。11例报告]
Zhonghua Nei Ke Za Zhi. 1992 Oct;31(10):639-41, 659.
7
PMA induces platelet activation of specific antigens (CD62/CD63) in GpIIb-IIIa deficient platelets from Glanzmann's thrombasthenia.佛波酯可诱导来自Glanzmann血小板无力症患者的糖蛋白IIb-IIIa缺陷血小板中特定抗原(CD62/CD63)的血小板活化。
Platelets. 1997;8(6):391-5. doi: 10.1080/09537109777078.
8
Different biochemical expression pattern of platelet surface glycoproteins suggests molecular diversity of Glanzmann's thrombasthenia in Iran.血小板表面糖蛋白不同的生化表达模式提示伊朗Glanzmann血小板无力症存在分子多样性。
Blood Coagul Fibrinolysis. 2013 Sep;24(6):613-8. doi: 10.1097/MBC.0b013e328360a558.
9
[Analysis of the GPIIb and GPIIIa genes in patients with Glanzmann's thrombasthenia].
Rinsho Ketsueki. 1992 Feb;33(2):133-8.
10
A variant of Glanzmann's thrombasthenia characterized by abnormal glycoprotein IIb/IIIa complex formation.一种以糖蛋白IIb/IIIa复合物形成异常为特征的Glanzmann血小板无力症变体。
Thromb Haemost. 1989 Nov 24;62(3):977-83.