• 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

从4细胞和8细胞小鼠卵中分离出的卵裂球的植入后发育。

Postimplantation development of blastomeres isolated from 4- and 8-cell mouse eggs.

作者信息

Rossant J

出版信息

J Embryol Exp Morphol. 1976 Oct;36(2):283-90.

PMID:1033982
Abstract

Blastomeres isolated from 4- and 8-cell mouse eggs were inserted into empty zonae and transferred to the oviduct. The products of both types of blastomere were capable of inducing decidual formation. One implant produced by an isolated blastomere from a 4-cell egg contained a small, retarded embryo at 5 1/2 days but most decidua from blastomeres of either 4- or 8-cell eggs contained only a few trophoblast giant cells. It is suggested that this lack of totipotency is due to insufficient cells being present at cavitation rather than restriction in developmental potential.

摘要

从4细胞和8细胞小鼠卵中分离出的卵裂球被植入空透明带并转移至输卵管。两种类型卵裂球的产物都能够诱导蜕膜形成。一个由4细胞卵的分离卵裂球产生的植入物在5.5天时含有一个小的、发育迟缓的胚胎,但来自4细胞或8细胞卵的卵裂球形成的大多数蜕膜仅含有少数滋养层巨细胞。有人提出,这种全能性的缺乏是由于在空泡化时细胞数量不足,而不是发育潜能受到限制。

相似文献

1
Postimplantation development of blastomeres isolated from 4- and 8-cell mouse eggs.从4细胞和8细胞小鼠卵中分离出的卵裂球的植入后发育。
J Embryol Exp Morphol. 1976 Oct;36(2):283-90.
2
[Mechanisms and frequency of nuclear divisions in trophoblast and decidua cells during postimplantation embryogenesis in the mouse].[小鼠植入后胚胎发育过程中滋养层和蜕膜细胞的核分裂机制及频率]
Ontogenez. 2003 Nov-Dec;34(6):472-7.
3
Structural and functional properties of trophoblast cells of mouse egg-cylinders in vitro.体外培养的小鼠卵柱滋养层细胞的结构和功能特性
Anat Rec. 1993 Jun;236(2):417-24. doi: 10.1002/ar.1092360217.
4
Deviation of the blastocyst axis from the first cleavage plane does not affect the quality of mouse postimplantation development.
Biol Reprod. 2003 Oct;69(4):1208-12. doi: 10.1095/biolreprod.103.018283. Epub 2003 May 28.
5
Unbiased contribution of the first two blastomeres to mouse blastocyst development.前两个卵裂球对小鼠囊胚发育的无偏贡献。
Mol Reprod Dev. 2005 Nov;72(3):354-61. doi: 10.1002/mrd.20353.
6
Analysis of cell lineage in two- and four-cell mouse embryos.对二细胞和四细胞小鼠胚胎的细胞谱系分析。
Development. 2003 Nov;130(21):5113-22. doi: 10.1242/dev.00725. Epub 2003 Aug 27.
7
Investigation of the determinative state of the mouse inner cell mass. II. The fate of isolated inner cell masses transferred to the oviduct.
J Embryol Exp Morphol. 1975 Jul;33(4):991-1001.
8
Developmental pattern of hexaploid mouse embryos produced by blastomere fusion of diploid and tetraploid embryos at the 2-cell stage.二倍体和四倍体胚胎在2细胞期通过卵裂球融合产生的六倍体小鼠胚胎的发育模式。
Zygote. 2009 May;17(2):125-30. doi: 10.1017/S0967199409005206. Epub 2009 Feb 23.
9
Postimplantation development of mitomycin C-treated mouse blastocysts.丝裂霉素C处理的小鼠囊胚植入后的发育
Teratology. 1988 Mar;37(3):205-12. doi: 10.1002/tera.1420370305.
10
Impact of the presence of one or more multinucleated blastomeres on the developmental potential of the embryo to the blastocyst stage.
Fertil Steril. 2005 Jan;83(1):243-5. doi: 10.1016/j.fertnstert.2004.08.016.

引用本文的文献

1
Mouse and human embryonic genome activation initiate at the one-cell stage.小鼠和人类胚胎基因组激活始于单细胞阶段。
Front Cell Dev Biol. 2025 Jul 30;13:1594995. doi: 10.3389/fcell.2025.1594995. eCollection 2025.
2
coordinately promotes metabolic shift and regulates totipotency exit.协同促进代谢转变并调节全能性退出。
Life Med. 2025 Mar 14;4(3):lnaf013. doi: 10.1093/lifemedi/lnaf013. eCollection 2025 Jun.
3
Loss of KANSL3 leads to defective inner cell mass and early embryonic lethality.KANSL3 的缺失导致内细胞团缺陷和早期胚胎致死。
Mol Reprod Dev. 2024 May;91(5):e23760. doi: 10.1002/mrd.23760.
4
A comprehensive review: synergizing stem cell and embryonic development knowledge in mouse and human integrated stem cell-based embryo models.全面综述:在基于小鼠和人类整合干细胞的胚胎模型中融合干细胞与胚胎发育知识
Front Cell Dev Biol. 2024 Apr 22;12:1386739. doi: 10.3389/fcell.2024.1386739. eCollection 2024.
5
Seeking arrangements: cell contact as a cleavage-stage biomarker.寻求安排:细胞接触作为卵裂期生物标志物。
Reprod Biomed Online. 2024 Mar;48(3):103654. doi: 10.1016/j.rbmo.2023.103654. Epub 2023 Nov 3.
6
Lineage regulators TFAP2C and NR5A2 function as bipotency activators in totipotent embryos.谱系调控因子 TFAP2C 和 NR5A2 在全能胚胎中作为多能性激活剂发挥作用。
Nat Struct Mol Biol. 2024 Jun;31(6):950-963. doi: 10.1038/s41594-023-01199-x. Epub 2024 Jan 19.
7
NR5A2 connects zygotic genome activation to the first lineage segregation in totipotent embryos.NR5A2 将合子基因组激活与全能胚胎中的第一个谱系分离连接起来。
Cell Res. 2023 Dec;33(12):952-966. doi: 10.1038/s41422-023-00887-z. Epub 2023 Nov 7.
8
Bilineage embryo-like structure from EPS cells can produce live mice with tetraploid trophectoderm.来源于 ESCs 的双系胚胎样结构可产生具有四倍体滋养外胚层的活鼠。
Protein Cell. 2023 Apr 21;14(4):262-278. doi: 10.1093/procel/pwac029.
9
Genome architecture and totipotency: An intertwined relation during early embryonic development.基因组结构与全能性:胚胎早期发育中的相互交织关系。
Bioessays. 2022 Jul;44(7):e2200029. doi: 10.1002/bies.202200029. Epub 2022 May 13.
10
Epigenetic, genetic and maternal effects enable stable centromere inheritance.表观遗传、遗传和母体效应使着丝粒的稳定遗传成为可能。
Nat Cell Biol. 2022 May;24(5):748-756. doi: 10.1038/s41556-022-00897-w. Epub 2022 May 9.