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首页> 外文期刊>The Journal of Reproduction and Development >Vitrification of porcine cumulus-oocyte complexes at the germinal vesicle stage does not trigger apoptosis in oocytes and early embryos, but activates anti-apoptotic Bcl-XL gene expression beyond the 4-cell stage
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Vitrification of porcine cumulus-oocyte complexes at the germinal vesicle stage does not trigger apoptosis in oocytes and early embryos, but activates anti-apoptotic Bcl-XL gene expression beyond the 4-cell stage

机译:生发囊泡阶段的猪积云络合物的玻璃化不会引发卵母细胞和早期胚胎中的凋亡,但在4细胞阶段激活抗凋亡Bcl-XL基因表达

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摘要

The aim of the present study was to clarify whether or not our vitrification procedure at the germinal vesicle (GV)-stage triggers the apoptotic cascade in oocytes and subsequent embryos. Immature porcine cumulus-oocyte complexes were either vitrified and warmed (vitrified group) or subjected to cryoprotectant agents (CPA group) or cultured without any treatment (control). Oocytes of all treatment groups were subjected to in vitro maturation (IVM), fertilization, and embryo culture. Apoptosis was assayed in live oocytes at the end of IVM culture and in cleavage-stage embryos after in vitro fertilization (IVF). We detected similar frequencies of DNA fragmentation, levels of caspase activity, phosphatidylserine externalization, and mRNA levels for pro-apoptotic Bax and CASP3 genes in oocytes at the end of IVM and in early embryos among all groups. However, in the vitrified group, the anti-apoptotic Bcl-XL gene was upregulated in 4–8 cell embryos, which caused an 8-fold significant increase in the Bcl-XL / Bax mRNA ratio compared with the control and CPA groups (P 0.05). In conclusion, vitrification of porcine oocytes at the GV stage by our method did not trigger the apoptotic cascade in oocytes and subsequent embryos but triggered the upregulation of the anti-apoptotic Bcl-XL gene in embryos.
机译:本研究的目的是阐明我们在发芽剂(GV)的玻璃化程序是否触发卵母细胞和随后的胚胎中的凋亡级联。未成熟的猪巨核卵母细胞配合物是玻璃化和温热的(vitrized基团),或进行冷冻保护剂(CPA组)或培养而不治疗(对照)。所有治疗组的卵母细胞进行体外成熟(IVM),施肥和胚胎培养物。在体外施肥(IVF)后,在IVM培养物结束和切割阶段胚胎中测定细胞凋亡。我们检测到类似频率的DNA碎片,胱天蛋白酶活性,磷脂酰杂鼠外化和MRNA水平,在IVM末端和卵母细胞中的卵凋亡Bax和Casp3基因的MRNA水平和所有组中的早期胚胎。然而,在玻璃化基团中,抗凋亡Bcl-XL基因在4-8个细胞胚胎中升高,与对照和CPA组相比,在Bcl-XL / Bax mRNA比中引起8倍的显着增加(P. <0.05)。总之,通过我们的方法在GV阶段的猪卵母细胞的玻璃化未触发卵母细胞中的凋亡级联和随后的胚胎,但引发胚胎中抗凋亡Bcl-XL基因的上调。

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