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本文引用的文献

1
Granulosa cell ligand NPPC and its receptor NPR2 maintain meiotic arrest in mouse oocytes.颗粒细胞配体 NPPC 及其受体 NPR2 维持小鼠卵母细胞减数分裂阻滞。
Science. 2010 Oct 15;330(6002):366-9. doi: 10.1126/science.1193573.
2
Cumulus cell contact during oocyte maturation in mice regulates meiotic spindle positioning and enhances developmental competence.在小鼠卵母细胞成熟过程中,卵丘细胞的接触调节着减数分裂纺锤体的定位,并增强了胚胎的发育能力。
J Assist Reprod Genet. 2010 Jan;27(1):29-39. doi: 10.1007/s10815-009-9376-9. Epub 2009 Dec 29.
3
A novel two-step strategy for in vitro culture of early-stage ovarian follicles in the mouse.一种新型两步法体外培养小鼠早期卵巢卵泡。
Fertil Steril. 2010 May 15;93(8):2633-9. doi: 10.1016/j.fertnstert.2009.10.027. Epub 2009 Dec 11.
4
Cyclic GMP signaling is involved in the luteinizing hormone-dependent meiotic maturation of mouse oocytes.环鸟苷酸信号参与了依赖黄体生成素的小鼠卵母细胞减数分裂成熟。
Biol Reprod. 2009 Sep;81(3):595-604. doi: 10.1095/biolreprod.109.077768. Epub 2009 May 27.
5
Cyclic GMP from the surrounding somatic cells regulates cyclic AMP and meiosis in the mouse oocyte.来自周围体细胞的环鸟苷酸调节小鼠卵母细胞中的环腺苷酸和减数分裂。
Development. 2009 Jun;136(11):1869-78. doi: 10.1242/dev.035238.
6
Mouse oocyte control of granulosa cell development and function: paracrine regulation of cumulus cell metabolism.小鼠卵母细胞对颗粒细胞发育和功能的控制:卵丘细胞代谢的旁分泌调节。
Semin Reprod Med. 2009 Jan;27(1):32-42. doi: 10.1055/s-0028-1108008. Epub 2009 Feb 5.
7
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources.利用DAVID生物信息学资源对大型基因列表进行系统和综合分析。
Nat Protoc. 2009;4(1):44-57. doi: 10.1038/nprot.2008.211.
8
Oocyte regulation of metabolic cooperativity between mouse cumulus cells and oocytes: BMP15 and GDF9 control cholesterol biosynthesis in cumulus cells.小鼠卵丘细胞与卵母细胞之间代谢协同性的卵母细胞调控:骨形态发生蛋白15和生长分化因子9控制卵丘细胞中的胆固醇生物合成。
Development. 2008 Jan;135(1):111-21. doi: 10.1242/dev.009068. Epub 2007 Nov 28.
9
Tissue-engineered follicles produce live, fertile offspring.组织工程化卵泡产生了存活且可育的后代。
Tissue Eng. 2006 Oct;12(10):2739-46. doi: 10.1089/ten.2006.12.2739.
10
Identification of a stage-specific permissive in vitro culture environment for follicle growth and oocyte development.确定卵泡生长和卵母细胞发育阶段特异性的体外许可培养环境。
Biol Reprod. 2006 Dec;75(6):916-23. doi: 10.1095/biolreprod.106.054833. Epub 2006 Sep 6.

在基于藻酸盐的培养系统中进行体外卵泡发育后,小鼠的减数分裂和发育能力受到损害。

Meiotic and developmental competence in mice are compromised following follicle development in vitro using an alginate-based culture system.

机构信息

Reproductive Endocrinology and Infertility, Departments of Obstetrics and Gynecology University of Pennsylvania, Philadelphia, PA 19104-6018, USA.

出版信息

Biol Reprod. 2011 Aug;85(2):269-76. doi: 10.1095/biolreprod.111.091124. Epub 2011 Apr 13.

DOI:10.1095/biolreprod.111.091124
PMID:21490243
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3142256/
Abstract

Culture systems that support development and maturation of oocytes in vitro with a high efficiency would have great impact not only on research addressed at underlying mechanisms of oocyte development but also on preservation of fertility. Recently, attention has turned to using culture systems that preserve follicle integrity, in contrast to existing systems that do not maintain follicle integrity, with the hope of improving oocyte development. We report that an alginate-based follicle culture system supports both follicular and oocyte growth in vitro, with little effect on the oocyte transcriptome. Nevertheless, oocytes obtained from these follicles exhibit an increased incidence of defects in spindle formation and chromosome alignment as well as pronounced abnormalities in cortical granule biogenesis. Developmental competence is also highly compromised, because few matured oocytes develop into 1-cell embryos with pronuclei. This situation contrasts with a high incidence of pronuclear formation following development using an existing in vitro culture system that does not preserve follicle integrity.

摘要

体外高效支持卵母细胞发育和成熟的培养体系不仅对研究卵母细胞发育的潜在机制具有重大影响,而且对保存生育能力也具有重大影响。最近,人们关注的焦点转向使用能够保持卵泡完整性的培养体系,而不是现有的不保持卵泡完整性的培养体系,希望能改善卵母细胞的发育。我们报告称,基于藻酸盐的卵泡培养体系支持体外卵泡和卵母细胞的生长,对卵母细胞的转录组几乎没有影响。然而,从这些卵泡中获得的卵母细胞在纺锤体形成和染色体排列方面出现缺陷的发生率增加,皮质颗粒发生也有明显异常。发育能力也受到严重损害,因为很少有成熟的卵母细胞能发育成具有原核的 1 细胞胚胎。这种情况与使用不保持卵泡完整性的现有体外培养系统进行发育时原核形成的高发生率形成鲜明对比。