首页> 外文期刊>Czech Journal of Animal Science >Transcript analysis of Heat shock protein 72 and protein 53 of 4-cell mouse embryos following Cryotop vitrification
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Transcript analysis of Heat shock protein 72 and protein 53 of 4-cell mouse embryos following Cryotop vitrification

机译:Cryotop玻璃化后4细胞小鼠胚胎热休克蛋白72和53的转录本分析

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摘要

The effects of two different concentrations of cryoprotectants on survival and developmental capacity of four-cell mouse embryos were compared by Cryotop vitrification to demonstrate that lower concentrations provide the same results as higher previously reported concentrations with lesser negative molecular impact on embryo cells. For this latest, embryos were compared via transcript analyses of Heat shock protein 72 (Hsp72) and protein 53 (p53). Four-cell embryos were obtained from superovulated female mice and randomly assigned to one of three following groups: (i) control (non-vitrified), (ii) vitx (15% v/v: 7.5% ethylene glycol (EG) and 7.5% dimethyl sulfoxide (DMSO), and (Hi) vit> (30% v/v: 15% EG + 15% DMSO). The cells vitrified by Cryotop were thawed and side-by-side to the control group divided into two parts: one part was used to analyze the morphological traits, survival rate, and embryo cleavage ability to form blastocysts, and the other part was examined for changes in transcript levels of Hsp72 (Hspala + Hspalb), p53, and Hprtl (reference gene) by quantitative Real-Time polymerase chain reaction (qPCR). The results were analyzed by One Way Analysis of Variance and the mean values compared with LSD (P < 0.05). The relative expressionof pS3 in vit_2 (30% v/v) was significantly higher than in vit_1 (15% v/v) and in vit_1 it was higher than in the control. The relative expression of Hsp72 was the same in vit_1 and vit_2 and significantly higher than in the control. The survival, cleavage, and blastocyst rates were the same for both vitrification treatments and significantly lower than in the control group. The up-regulations of Hsp72 and p53 following vitrification were suggestive of imposed heat shock, cold stress, and DNA damage tothe mouse 4-cell embryos.
机译:通过Cryotop玻璃化比较了两种不同浓度的冷冻保护剂对四细胞小鼠胚胎存活和发育能力的影响,以证明较低的浓度可提供与先前报道的较高浓度相同的结果,而对胚胎细胞的负面分子影响较小。为此,通过热休克蛋白72(Hsp72)和蛋白53(p53)的转录本分析比较了胚胎。从超排卵的雌性小鼠中获得四细胞胚胎,并将其随机分为以下三组之一:(i)对照(非玻璃化),(ii)vitx(15%v / v:7.5%乙二醇(EG)和7.5 %二甲基亚砜(DMSO)和(Hi)vit>(30%v / v:15%EG + 15%DMSO)。将经Cryotop玻璃化的细胞解冻,并与对照组并排,分为两部分:一部分用于分析形态特征,成活率和胚胎裂解形成胚泡的能力,另一部分用于检测Hsp72(Hspala + Hspalb),p53和Hprtl(参考基因)的转录水平的变化定量实时聚合酶链反应(qPCR)。用方差单向分析法分析结果,平均值与LSD进行比较(P <0.05)。pS3在vit_2中的相对表达(30%v / v)明显更高与vit_1(v / v为15%)相比,在vit_1中高于对照。Hsp72的相对表达在vit_1和vit_中相同2,明显高于对照组。两种玻璃化治疗的存活率,卵裂率和囊胚率均相同,且显着低于对照组。玻璃化后Hsp72和p53的上调提示对小鼠4细胞胚胎施加了热休克,冷应激和DNA损伤。

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