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玻璃化冷冻-解冻牛卵母细胞中凋亡基因的表达模式

Expression pattern of apoptotic genes in vitrified-thawed bovine oocytes.

作者信息

Anchamparuthy V M, Pearson R E, Gwazdauskas F C

机构信息

Department of Dairy Science, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA.

出版信息

Reprod Domest Anim. 2010 Oct;45(5):e83-90. doi: 10.1111/j.1439-0531.2009.01527.x.

DOI:10.1111/j.1439-0531.2009.01527.x
PMID:19821945
Abstract

This study describes a method for quantification of transcripts from low numbers of bovine oocytes using real time RT-PCR. The objective was to evaluate the expression pattern of apoptotic genes (Fas, FasL, Bax and Bcl-2) in vitrified-thawed oocytes. Oocytes were evaluated at germinal vesicle stage; at 15 h of maturation; after vitrification and warming at 15 h of maturation and at 9 h of additional maturation. All transcripts showed an increase in at least 1.2-fold change post-vitrification warming, but the levels tended to decrease at 9 h of maturation post-vitrification warming. Transcript abundance for Fas mRNA was 1.4-fold for oocytes after vitrification and warming. The level of Fas mRNA upon maturation was 0.8-fold. The increase in the abundance of FasL mRNA was 2.1, while it was 0.5-fold relative to control. Vitrification resulted in 1.5-fold change in Bax mRNA expression in oocytes. After 9 h of maturation post-vitrification warming, the level for Bax mRNA was 0.6-fold. The mRNA for Bcl-2 was nearly the same after vitrification and warming. The abundance of mRNA for Bcl-2 was 1.2-fold in vitrified oocytes and fell (p = 0.05) to 0.5 at 9 h of maturation post-vitrification and warming. The up-regulation of apoptotic genes in vitrified oocytes may be an early indicator of reduced developmental competence following vitrification. Yet, results from terminal deoxynucleotidyl transferase dUTP nick end labelling and caspase assays did not support the evidence of apoptosis in embryos derived from large numbers of vitrified oocytes.

摘要

本研究描述了一种使用实时逆转录聚合酶链反应(RT-PCR)对少量牛卵母细胞转录本进行定量的方法。目的是评估玻璃化冷冻-解冻卵母细胞中凋亡基因(Fas、FasL、Bax和Bcl-2)的表达模式。在生发泡期、成熟15小时、玻璃化冷冻并在成熟15小时及额外成熟9小时后复温时对卵母细胞进行评估。所有转录本在玻璃化冷冻复温后均显示至少1.2倍的变化增加,但在玻璃化冷冻复温后成熟9小时时水平趋于下降。玻璃化冷冻复温后卵母细胞中Fas mRNA的转录本丰度为1.4倍。成熟时Fas mRNA的水平为0.8倍。FasL mRNA丰度的增加为2.1倍,而相对于对照为0.5倍。玻璃化冷冻导致卵母细胞中Bax mRNA表达有1.5倍的变化。玻璃化冷冻复温后成熟9小时,Bax mRNA的水平为0.6倍。玻璃化冷冻复温后Bcl-2的mRNA几乎相同。玻璃化冷冻卵母细胞中Bcl-2 mRNA的丰度为1.2倍,在玻璃化冷冻复温后成熟9小时时降至0.5倍(p = 0.05)。玻璃化冷冻卵母细胞中凋亡基因的上调可能是玻璃化冷冻后发育能力降低的早期指标。然而,末端脱氧核苷酸转移酶dUTP缺口末端标记和半胱天冬酶检测结果并不支持来自大量玻璃化冷冻卵母细胞的胚胎存在凋亡的证据。

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