• 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

补体调节蛋白在人类卵子和植入前胚胎上的表达。

Expression of complement regulatory proteins on human eggs and preimplantation embryos.

作者信息

Fenichel P, Donzeau M, Cervoni F, Menezo Y, Hsi B L

机构信息

INSERM U364, Faculté de Médecine, Nice, France.

出版信息

Am J Reprod Immunol. 1995 Feb;33(2):155-64. doi: 10.1111/j.1600-0897.1995.tb00879.x.

DOI:10.1111/j.1600-0897.1995.tb00879.x
PMID:7544131
Abstract

PROBLEM

To investigate the relation between the complement system and reproduction, expression of complement regulatory proteins (C3b receptors and inhibitor of the membrane attack complex) were screened on unfixed human eggs and preimplantation embryos.

METHODS

Unfixed unfertilized oocytes and preimplantation embryos obtained from an in vitro fertilization program were stained by indirect immunofluorescence using monoclonal antibodies raised against membrane cofactor protein, (MCP or CD46), decay accelerating factor (DAF or CD55), protectin (CD59), human C3b/C4b receptor (CR1 or CD35), and major histocompatibility complex class I antigen (MHC class I).

RESULTS

CD55 and CD59 were both expressed by the plasma membrane of unfertilized oocytes and pre-implantation embryos. CD46 was not expressed by unfertilized oocytes but appeared at the 6-to-8 cell stage embryo when human gene expression first occurs. CD35 and MHC class I antigens were not expressed at all on oocytes and preimplantation embryos.

CONCLUSIONS

Selective expression of complement regulatory proteins (DAF and protectin) associated with the lack of MHC class I antigens may represent an immune protective mechanism by which human oocytes and preimplantation embryos escape complement-mediated damage during their travel through the female genital tract. Furthermore, participation of these complement regulatory proteins including MCP in cell to cell interaction during fertilization and/or implantation cannot be excluded.

摘要

问题

为研究补体系统与生殖之间的关系,对未固定的人类卵子和植入前胚胎上补体调节蛋白(C3b受体和膜攻击复合物抑制剂)的表达进行筛选。

方法

从体外受精程序中获取的未固定未受精卵母细胞和植入前胚胎,使用针对膜辅因子蛋白(MCP或CD46)、衰变加速因子(DAF或CD55)、保护素(CD59)、人C3b/C4b受体(CR1或CD35)和主要组织相容性复合体I类抗原(MHC I类)的单克隆抗体,通过间接免疫荧光进行染色。

结果

未受精卵母细胞和植入前胚胎的质膜均表达CD55和CD59。未受精卵母细胞不表达CD46,但在人类基因表达首次出现的6至8细胞期胚胎时出现。卵母细胞和植入前胚胎上完全不表达CD35和MHC I类抗原。

结论

与缺乏MHC I类抗原相关的补体调节蛋白(DAF和保护素)的选择性表达,可能代表一种免疫保护机制,通过该机制人类卵母细胞和植入前胚胎在通过女性生殖道的过程中逃避补体介导的损伤。此外,不能排除这些补体调节蛋白(包括MCP)在受精和/或植入过程中的细胞间相互作用中发挥作用。

相似文献

1
Expression of complement regulatory proteins on human eggs and preimplantation embryos.补体调节蛋白在人类卵子和植入前胚胎上的表达。
Am J Reprod Immunol. 1995 Feb;33(2):155-64. doi: 10.1111/j.1600-0897.1995.tb00879.x.
2
[Expression and role of complement regulatory proteins on human gametes and pre-implantation embryos].补体调节蛋白在人类配子和植入前胚胎上的表达及作用
Contracept Fertil Sex. 1995 Sep;23(9):576-80.
3
Complement-binding proteins are strongly expressed by human preimplantation blastocysts and cumulus cells as well as gametes.补体结合蛋白在人类植入前囊胚、卵丘细胞以及配子中均有强烈表达。
Mol Hum Reprod. 1996 Jan;2(1):52-9. doi: 10.1093/molehr/2.1.52.
4
Expression of complement regulatory proteins [membrane cofactor protein (CD46), decay accelerating factor (CD55), and protectin (CD59)] in endometrial stressed cells.补体调节蛋白[膜辅因子蛋白(CD46)、衰变加速因子(CD55)和保护素(CD59)]在子宫内膜应激细胞中的表达。
Cell Immunol. 2003 May;223(1):46-51. doi: 10.1016/s0008-8749(03)00127-8.
5
The expression of the complement regulators CD46, CD55, and CD59 by human sperm does not protect them from antisperm antibody- and complement-mediated immune injury.人类精子表面补体调节蛋白CD46、CD55和CD59的表达并不能保护它们免受抗精子抗体和补体介导的免疫损伤。
Fertil Steril. 1993 Apr;59(4):876-84. doi: 10.1016/s0015-0282(16)55875-0.
6
Identification of the complement regulatory proteins CD46, CD55, and CD59 in human fallopian tube, endometrium, and cervical mucosa and secretion.在人输卵管、子宫内膜及宫颈黏膜和分泌物中补体调节蛋白CD46、CD55和CD59的鉴定。
Am J Reprod Immunol. 1995 Jul;34(1):1-9. doi: 10.1111/j.1600-0897.1995.tb00913.x.
7
Complement regulatory proteins at the feto-maternal interface during human placental development: distribution of CD59 by comparison with membrane cofactor protein (CD46) and decay accelerating factor (CD55).人类胎盘发育过程中母胎界面的补体调节蛋白:CD59与膜辅因子蛋白(CD46)和衰变加速因子(CD55)的分布比较
Eur J Immunol. 1992 Jun;22(6):1579-85. doi: 10.1002/eji.1830220635.
8
Expression of the CD46 antigen, and absence of class I MHC antigen, on the human oocyte and preimplantation blastocyst.人类卵母细胞和植入前胚泡上CD46抗原的表达及I类主要组织相容性复合体抗原的缺失。
Immunology. 1992 Jan;75(1):202-5.
9
The change of membrane complement regulatory protein in chorion of early pregnancy.
Clin Immunol Immunopathol. 1993 Nov;69(2):167-74. doi: 10.1006/clin.1993.1166.
10
Human lung cancer cell lines express cell membrane complement inhibitory proteins and are extremely resistant to complement-mediated lysis; a comparison with normal human respiratory epithelium in vitro, and an insight into mechanism(s) of resistance.人肺癌细胞系表达细胞膜补体抑制蛋白,对补体介导的细胞溶解具有极强的抗性;体外与人正常呼吸道上皮的比较及抗性机制的探究。
Clin Exp Immunol. 1998 Aug;113(2):173-82. doi: 10.1046/j.1365-2249.1998.00581.x.

引用本文的文献

1
The complement system in human pregnancy and preeclampsia.人类妊娠和子痫前期中的补体系统。
Front Immunol. 2025 Aug 19;16:1617140. doi: 10.3389/fimmu.2025.1617140. eCollection 2025.
2
Proteomic and Bioinformatic Analysis of Decellularized Pancreatic Extracellular Matrices.去细胞化胰腺细胞外基质的蛋白质组学和生物信息学分析。
Molecules. 2021 Nov 8;26(21):6740. doi: 10.3390/molecules26216740.
3
Complement in Human Pre-implantation Embryos: Attack and Defense.人类着床前胚胎中的补体:攻击与防御。
Front Immunol. 2019 Sep 18;10:2234. doi: 10.3389/fimmu.2019.02234. eCollection 2019.
4
Evaluation of preincubation time interval in testicular biopsy to obtain optimum sperm parameters.评价睾丸活检前孵育时间间隔以获得最佳精子参数。
Cell J. 2012 Spring;14(1):1-6. Epub 2012 Jun 13.
5
Restriction of GAGE protein expression to subpopulations of cancer cells is independent of genotype and may limit the use of GAGE proteins as targets for cancer immunotherapy.
Br J Cancer. 2006 Jun 19;94(12):1864-73. doi: 10.1038/sj.bjc.6603163.
6
Decay accelerating factor in guinea-pig reproductive organs.豚鼠生殖器官中的衰变加速因子。
Immunology. 2000 May;100(1):91-8. doi: 10.1046/j.1365-2567.2000.00010.x.