• 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

孕期母体内造血器官中胎儿细胞的浓度。小鼠实验研究(作者译)

[The concentration of fetal cells in maternal haematopoietic organs during pregnancy. An experimental study in mice (author's transl)].

作者信息

Gaillard M C, Ouvre E, Liégeois A, Lewin D

出版信息

J Gynecol Obstet Biol Reprod (Paris). 1978 Sep;7(6):1043-50.

PMID:730985
Abstract

We have been able to show that fetal cells are able to survive and multiply in the haematopoietic organs of the pregnant mouse. We have been able to label fetal cells with a chromosome marker (T6) which is clearly visible in the metaphase of mitosis. It is not only that there is a considerable concentration of fetal cells in the maternal spleen (3 to 6 per cent) but there are several factors that suggest that these fetal cells can multiply there. These are, the presence of mitoses, long survival, and a rise in numbers in the case of a new pregnancy. Thus pregnancy seems to bring about a physiological "microchimerism".

摘要

我们已经能够证明,胎儿细胞能够在怀孕小鼠的造血器官中存活并增殖。我们已经能够用一种染色体标记(T6)标记胎儿细胞,这种标记在有丝分裂中期清晰可见。不仅母体脾脏中有相当数量的胎儿细胞(3%至6%),而且有几个因素表明这些胎儿细胞能够在那里增殖。这些因素包括有丝分裂的存在、长期存活以及再次怀孕时数量的增加。因此,怀孕似乎会导致一种生理性的“微嵌合体”。

相似文献

1
[The concentration of fetal cells in maternal haematopoietic organs during pregnancy. An experimental study in mice (author's transl)].孕期母体内造血器官中胎儿细胞的浓度。小鼠实验研究(作者译)
J Gynecol Obstet Biol Reprod (Paris). 1978 Sep;7(6):1043-50.
2
Microchimerism in pregnant mice.怀孕小鼠中的微嵌合体现象。
Transplant Proc. 1981 Mar;13(1 Pt 2):1250-2.
3
Fetal cell microchimerism develops through the migration of fetus-derived cells to the maternal organs early after implantation.胎儿细胞微嵌合体通过胎儿来源的细胞在着床后早期向母体器官迁移而发展。
J Reprod Immunol. 2010 Mar;84(2):117-23. doi: 10.1016/j.jri.2009.11.006. Epub 2010 Jan 29.
4
Hemopoietic origin of certain decidual cell precursors in murine pregnancy.小鼠妊娠中某些蜕膜细胞前体的造血起源。
Am J Anat. 1989 May;185(1):9-18. doi: 10.1002/aja.1001850103.
5
Fetal microchimerism in the maternal mouse brain: a novel population of fetal progenitor or stem cells able to cross the blood-brain barrier?母鼠大脑中的胎儿微嵌合体:一类能够穿越血脑屏障的新型胎儿祖细胞或干细胞?
Stem Cells. 2005 Nov-Dec;23(10):1443-52. doi: 10.1634/stemcells.2004-0169. Epub 2005 Aug 9.
6
The maternal immune system's interaction with circulating fetal cells.母体免疫系统与循环胎儿细胞的相互作用。
J Immunol. 1997 Jan 1;158(1):40-7.
7
Fetal cell microchimerism in tissue from multiple sites in women with systemic sclerosis.系统性硬化症女性多个部位组织中的胎儿细胞微嵌合体
Arthritis Rheum. 2001 Aug;44(8):1848-54. doi: 10.1002/1529-0131(200108)44:8<1848::AID-ART323>3.0.CO;2-L.
8
Identification of CD4int progenitors in mouse fetal spleen, a source of resident lymphoid cells.小鼠胎儿脾脏中CD4int祖细胞的鉴定,一种常驻淋巴细胞的来源。
J Leukoc Biol. 2008 May;83(5):1145-54. doi: 10.1189/jlb.1107755. Epub 2008 Feb 12.
9
[Change in the proliferative activity of hematopoietic stem cells following adrenalectomy].[肾上腺切除术后造血干细胞增殖活性的变化]
Biull Eksp Biol Med. 1980 Mar;89(3):326-7.
10
Intrathyroidal fetal microchimerism in pregnancy and postpartum.
Endocrinology. 2002 Jan;143(1):247-53. doi: 10.1210/endo.143.1.8563.

引用本文的文献

1
The when, what, and where of naturally-acquired microchimerism.自然获得性微嵌合体的时间、内容和位置。
Semin Immunopathol. 2025 Mar 11;47(1):20. doi: 10.1007/s00281-024-01029-2.
2
Cell migration from baby to mother.细胞从婴儿向母亲迁移。
Cell Adh Migr. 2007 Jan-Mar;1(1):19-27. Epub 2007 Jan 28.
3
Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum.男性胎儿祖细胞在产后长达27年的时间里持续存在于母体血液中。
Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):705-8. doi: 10.1073/pnas.93.2.705.