Suppr超能文献

使用序贯培养基培养与极化或非极化子宫上皮细胞共培养的玻璃化冷冻复苏小鼠胚胎。

Development of vitrified-warmed mouse embryos co-cultured with polarized or non-polarized uterine epithelial cells using sequential culture media.

作者信息

Azadbakht Mehri, Valojerdi Mojtaba Rezazadeh

机构信息

Department of Anatomy, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

出版信息

J Assist Reprod Genet. 2008 Jun;25(6):251-61. doi: 10.1007/s10815-008-9231-4. Epub 2008 Jun 18.

Abstract

PURPOSE

To our knowledge, little is known about the effect of polarized and non-polarized uterine epithelial cells on cryopreserved embryo growth. This study was, therefore, set up to investigate the effect of these monolayers together with sequential culture media on vitrified-warmed mouse embryos in terms of blastocyst development, blastocyst quality, incidence of apoptosis and related genes expression.

METHODS

Two cell vitrified-warmed mouse embryos were cultured in G-1ver3 medium to the eight-cell stage when they were randomly assigned to three treatment groups of no co-culture (control), non-polarized and polarized mouse uterine epithelial monolayer co-culture. The culture medium was G-2ver3 during the treatment phase. After 96 h on treatment, the significance of differences were evaluated by the one way analysis of variance for continuous data.

RESULTS

In the polarized monolayer group, the hatched blastocyst formation and blastocyst quality improved significantly than other two groups (P < 0.05). Whereas the incidence of apoptosis and related gene expression such as Bax were higher in the blastocysts of control group (P < 0.05). The relative abundance of Bcl-2 mRNA to the beta-tubulin was similar for all treatments.

CONCLUSION

Co-culture system involving polarized uterine epithelial cells and sequential culture media is a promising method for the improvement of vitrified-warmed mouse embryo development.

摘要

目的

据我们所知,关于极化和非极化子宫上皮细胞对冷冻保存胚胎生长的影响知之甚少。因此,本研究旨在探讨这些单层细胞与序贯培养基对玻璃化冷冻复苏小鼠胚胎的囊胚发育、囊胚质量、凋亡发生率及相关基因表达的影响。

方法

将两组玻璃化冷冻复苏的小鼠胚胎在G-1ver3培养基中培养至八细胞期,然后随机分为三个处理组:无共培养组(对照组)、非极化小鼠子宫上皮单层共培养组和极化小鼠子宫上皮单层共培养组。处理阶段的培养基为G-2ver3。处理96小时后,采用单因素方差分析对连续数据进行差异显著性评估。

结果

在极化单层组中,孵化囊胚形成率和囊胚质量显著高于其他两组(P < 0.05)。而对照组囊胚的凋亡发生率及相关基因如Bax的表达较高(P < 0.05)。所有处理组中Bcl-2 mRNA与β-微管蛋白的相对丰度相似。

结论

涉及极化子宫上皮细胞和序贯培养基的共培养系统是改善玻璃化冷冻复苏小鼠胚胎发育的一种有前景的方法。

相似文献

2
Development of mouse embryos co-cultured with polarized or non-polarized uterine epithelial cells using sequential culture media.
Anim Reprod Sci. 2007 Jul;100(1-2):141-57. doi: 10.1016/j.anireprosci.2006.06.012. Epub 2006 Jul 28.
5
Effects of species and cellular activity of oviductal epithelial cells on their dialogue with co-cultured mouse embryos.
Cell Tissue Res. 2007 Jan;327(1):55-66. doi: 10.1007/s00441-006-0236-y. Epub 2006 Sep 2.
6
Effect of laser-assisted hatching and necrotic blastomere removal on the development of vitrified-warmed four-cell mouse embryos.
J Assist Reprod Genet. 2008 Jul;25(7):333-9. doi: 10.1007/s10815-008-9238-x. Epub 2008 Aug 8.
7
Effect of energy source during culture on in vitro embryo development, resistance to cryopreservation and sex ratio.
Theriogenology. 2011 Oct 15;76(7):1347-55. doi: 10.1016/j.theriogenology.2011.06.004. Epub 2011 Aug 6.
9
Uterine flushing with supernatant embryo culture medium in vitrified warmed blastocyst transfer cycles: a randomized controlled trial.
J Assist Reprod Genet. 2015 Feb;32(2):225-31. doi: 10.1007/s10815-014-0385-y. Epub 2014 Nov 27.
10
Open-pulled straw vitrification differentiates cryotolerance of in vitro cultured rabbit embryos at the eight-cell stage.
Theriogenology. 2011 Mar 1;75(4):760-8. doi: 10.1016/j.theriogenology.2010.10.018. Epub 2010 Dec 7.

引用本文的文献

本文引用的文献

1
Development of mouse embryos co-cultured with polarized or non-polarized uterine epithelial cells using sequential culture media.
Anim Reprod Sci. 2007 Jul;100(1-2):141-57. doi: 10.1016/j.anireprosci.2006.06.012. Epub 2006 Jul 28.
2
Overall efficiency of in vitro embryo production and vitrification in cattle.
Theriogenology. 1996 Feb;45(3):683-9. doi: 10.1016/0093-691x(95)00414-4.
3
Analysis of DNA fragmentation of porcine embryos exposed to cryoprotectants.
Reprod Domest Anim. 2005 Oct;40(5):429-32. doi: 10.1111/j.1439-0531.2005.00585.x.
6
Evidence of damage in cryopreserved and fresh bovine embryos using the Tunel technique.
Reprod Domest Anim. 2004 Jun;39(3):141-5. doi: 10.1111/j.1439-0531.2004.00492.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验