• 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

用纳米颗粒对胚胎进行体外标记。

In vitro tagging of embryos with nanoparticles.

作者信息

Fynewever Tricia L, Agcaoili Evelyn S, Jacobson John D, Patton William C, Chan Philip J

机构信息

Department of Gynecology and Obstetrics, Loma Linda University School of Medicine, Center for Fertility and IVF, 11370 Anderson Street, Suite 3950, Loma Linda, California 92354, USA.

出版信息

J Assist Reprod Genet. 2007 Feb-Mar;24(2-3):61-5. doi: 10.1007/s10815-006-9084-7. Epub 2006 Dec 29.

DOI:10.1007/s10815-006-9084-7
PMID:17195099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3454985/
Abstract

PURPOSE

To develop an in vitro method for tagging embryos and to compare the development of the embryos after nanoparticles injection versus externally-applied nanoparticles derived from either polystyrene or polyacrylonitrile.

METHODS

Each mouse 1-cell embryo (the selected test-model) was either: (a) injected by intracytoplasmic injection or (b) co-incubated with different nanoparticles at 37 degrees C, 5% CO2 in air. The embryos were assessed after 2 and 6 days of culture.

RESULTS

Embryo development was similar for externally-applied polystyrene nanoparticles and control (97.6 +/- 2.7 versus 100.0 +/- 0%) but different for polyacrylonitrile nanoparticles (90.0 +/- 2.8 %) on day 2. However, the results were similar on Day 6. Injected embryos were linked to lower percent development on Day 2. Few injected embryos reached blastocyst stage on Day 6 after a brief UV-fluorescence exposure.

CONCLUSIONS

Tagging embryos by external polystyrene-based nanoparticles was the better method when compared with injected nanoparticles. Larger nanoparticles in microsphere range were easier to qualitate. Inhibited hatching limited their use beyond the blastocyst stage.

摘要

目的

开发一种体外标记胚胎的方法,并比较纳米颗粒注射与外部施加源自聚苯乙烯或聚丙烯腈的纳米颗粒后胚胎的发育情况。

方法

将每个小鼠单细胞胚胎(所选测试模型)进行如下处理:(a) 通过胞浆内注射,或 (b) 在37℃、空气中5%二氧化碳条件下与不同纳米颗粒共同孵育。培养2天和6天后对胚胎进行评估。

结果

在第2天,外部施加的聚苯乙烯纳米颗粒与对照组的胚胎发育相似(97.6±2.7%对100.0±0%),但聚丙烯腈纳米颗粒不同(90.0±2.8%)。然而,在第6天结果相似。注射的胚胎在第2天发育百分比更低。短暂紫外线荧光照射后,很少有注射的胚胎在第6天达到囊胚阶段。

结论

与注射纳米颗粒相比,用基于聚苯乙烯的外部纳米颗粒标记胚胎是更好的方法。微球范围内较大的纳米颗粒更易于定性。孵化受抑制限制了它们在囊胚阶段之后的应用。

相似文献

1
In vitro tagging of embryos with nanoparticles.用纳米颗粒对胚胎进行体外标记。
J Assist Reprod Genet. 2007 Feb-Mar;24(2-3):61-5. doi: 10.1007/s10815-006-9084-7. Epub 2006 Dec 29.
2
Development of mammalian embryos exposed to mixed-size nanoparticles.暴露于不同尺寸混合纳米颗粒的哺乳动物胚胎发育情况。
Clin Exp Obstet Gynecol. 2005;32(4):222-4.
3
Barcode tagging of human oocytes and embryos to prevent mix-ups in assisted reproduction technologies.对人类卵子和胚胎进行条形码标记,以防止辅助生殖技术中出现混淆。
Hum Reprod. 2014 Jan;29(1):18-28. doi: 10.1093/humrep/det409. Epub 2013 Nov 13.
4
Cleavage kinetics analysis of human embryos predicts development to blastocyst and implantation.人类胚胎的卵裂动力学分析可预测胚胎发育至囊胚和着床。
Reprod Biomed Online. 2012 Nov;25(5):474-80. doi: 10.1016/j.rbmo.2012.07.016. Epub 2012 Aug 2.
5
Birth of nine normal healthy babies following transfer of blastocysts derived from human single-pronucleate zygotes.经人类单原核受精卵来源的囊胚移植后九个正常健康婴儿诞生。
J Assist Reprod Genet. 2015 Sep;32(9):1401-7. doi: 10.1007/s10815-015-0518-y. Epub 2015 Jun 26.
6
Influence of cell loss after vitrification or slow-freezing on further in vitro development and implantation of human Day 3 embryos.玻璃化或慢速冷冻后细胞丢失对人第三天胚胎体外进一步发育和植入的影响。
Hum Reprod. 2013 Nov;28(11):2943-9. doi: 10.1093/humrep/det356. Epub 2013 Sep 5.
7
[The protective effect of stem cell factor (SCF) on in vitro development of preimplantation mouse embryos].[干细胞因子(SCF)对小鼠植入前胚胎体外发育的保护作用]
Ann Acad Med Stetin. 2005;51(1):83-93.
8
Developmental kinetics of cleavage stage mouse embryos are related to their subsequent carbohydrate and amino acid utilization at the blastocyst stage.小鼠胚胎卵裂期的发育动力学与其随后在囊胚期对碳水化合物和氨基酸的利用有关。
Hum Reprod. 2015 Mar;30(3):543-52. doi: 10.1093/humrep/deu334. Epub 2015 Jan 6.
9
Attempts to enhance production of porcine chimeras from embryonic germ cells and preimplantation embryos.尝试提高从胚胎生殖细胞和植入前胚胎中生产猪嵌合体的效率。
Theriogenology. 2004 May;61(7-8):1225-35. doi: 10.1016/j.theriogenology.2003.06.007.
10
Effect of stem cell activation, culture media of manipulated embryos, and site of embryo transfer in the production of F0 embryonic stem cell mice.干细胞激活、操作后胚胎的培养基以及胚胎移植部位对F0胚胎干细胞小鼠产生的影响。
Biol Reprod. 2009 Jun;80(6):1216-22. doi: 10.1095/biolreprod.108.075044. Epub 2009 Feb 18.

引用本文的文献

1
The dual effects of nanomaterials on sperm and seminal fluid oxidative stress.纳米材料对精子和精液氧化应激的双重影响。
Mater Today Bio. 2025 Aug 5;34:102163. doi: 10.1016/j.mtbio.2025.102163. eCollection 2025 Oct.
2
Magnetic-Assisted Control of Eggs and Embryos via Zona Pellucida-Linked Nanoparticles.基于透明带连接纳米颗粒的磁控卵和胚胎。
Adv Sci (Weinh). 2024 May;11(18):e2306901. doi: 10.1002/advs.202306901. Epub 2024 Mar 6.
3
Research progress on the role and mechanism of DNA damage repair in germ cell development.DNA 损伤修复在生殖细胞发育中的作用及机制研究进展。
Front Endocrinol (Lausanne). 2023 Jul 17;14:1234280. doi: 10.3389/fendo.2023.1234280. eCollection 2023.
4
Applications of omics and nanotechnology to improve pig embryo production in vitro.组学和纳米技术在提高猪胚胎体外生产中的应用。
Mol Reprod Dev. 2019 Nov;86(11):1531-1547. doi: 10.1002/mrd.23260. Epub 2019 Sep 3.
5
Injection of ligand-free gold and silver nanoparticles into murine embryos does not impact pre-implantation development.将无配体的金和银纳米粒子注入到小鼠胚胎中不会影响胚胎的植入前发育。
Beilstein J Nanotechnol. 2014 May 21;5:677-88. doi: 10.3762/bjnano.5.80. eCollection 2014.
6
The Invasion and Reproductive Toxicity of QDs-Transferrin Bioconjugates on Preantral Follicle in vitro.QD-转铁蛋白生物缀合物对体外原始卵泡的入侵和生殖毒性。
Theranostics. 2012;2(7):734-45. doi: 10.7150/thno.4290. Epub 2012 Aug 1.
7
In Caenorhabditis elegans nanoparticle-bio-interactions become transparent: silica-nanoparticles induce reproductive senescence.在秀丽隐杆线虫中,纳米颗粒-生物相互作用变得清晰可见:二氧化硅纳米颗粒诱导生殖衰老。
PLoS One. 2009 Aug 12;4(8):e6622. doi: 10.1371/journal.pone.0006622.

本文引用的文献

1
Development of mammalian embryos exposed to mixed-size nanoparticles.暴露于不同尺寸混合纳米颗粒的哺乳动物胚胎发育情况。
Clin Exp Obstet Gynecol. 2005;32(4):222-4.
2
New tools for in vivo fluorescence tagging.用于体内荧光标记的新工具。
Curr Opin Plant Biol. 2005 Dec;8(6):565-73. doi: 10.1016/j.pbi.2005.09.011. Epub 2005 Sep 26.
3
Using a histone yellow fluorescent protein fusion for tagging and tracking endothelial cells in ES cells and mice.利用组蛋白黄色荧光蛋白融合技术标记和追踪胚胎干细胞及小鼠中的内皮细胞。
Genesis. 2005 Jul;42(3):162-71. doi: 10.1002/gene.20139.
4
Cytotoxicity of colloidal CdSe and CdSe/ZnS nanoparticles.胶体CdSe和CdSe/ZnS纳米颗粒的细胞毒性。
Nano Lett. 2005 Feb;5(2):331-8. doi: 10.1021/nl047996m.
5
Membrane toxicity accounts for apoptosis induced by realgar nanoparticles in promyelocytic leukemia HL-60 cells.膜毒性是雄黄纳米颗粒诱导早幼粒细胞白血病HL-60细胞凋亡的原因。
Biol Trace Elem Res. 2005 Feb;103(2):117-32. doi: 10.1385/BTER:103:2:117.
6
Green fluorescent protein tagging of extracellular signal-regulated kinase and p38 pathways reveals novel dynamics of pathway activation during primary and metastatic growth.细胞外信号调节激酶和p38信号通路的绿色荧光蛋白标记揭示了原发性和转移性生长过程中信号通路激活的新动态。
Cancer Res. 2004 Oct 15;64(20):7336-45. doi: 10.1158/0008-5472.CAN-04-0113.
7
On the cyto-toxicity caused by quantum dots.关于量子点引起的细胞毒性。
Microbiol Immunol. 2004;48(9):669-75. doi: 10.1111/j.1348-0421.2004.tb03478.x.
8
Translocation of inhaled ultrafine particles to the brain.吸入的超细颗粒向大脑的易位。
Inhal Toxicol. 2004 Jun;16(6-7):437-45. doi: 10.1080/08958370490439597.
9
Magnetic resonance tracking of transplanted bone marrow and embryonic stem cells labeled by iron oxide nanoparticles in rat brain and spinal cord.大鼠脑和脊髓中氧化铁纳米颗粒标记的移植骨髓和胚胎干细胞的磁共振追踪
J Neurosci Res. 2004 Apr 15;76(2):232-43. doi: 10.1002/jnr.20041.
10
A self-assembled, modular DNA delivery system mediated by silica nanoparticles.一种由二氧化硅纳米颗粒介导的自组装模块化DNA递送系统。
J Control Release. 2004 Mar 5;95(2):333-41. doi: 10.1016/j.jconrel.2003.11.019.