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Pig oocyte vitrification by Cryotop method and the activation of the apoptotic cascade.

机译:通过Cryotop方法对猪卵母细胞进行玻璃化,并激活凋亡级联反应。

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Oocyte and embryo cryopreservation has been applied successfully in many mammalian species. Nevertheless, pig oocytes, because of their greater susceptibility to cryoinjuries, have shown a reduced ability to be fertilized in vitro and a lower developmental competence. The aim of this study was to evaluate the apoptotic status of porcine oocytes vitrified by Cryotop method. We assessed three parameters linked to the activation of the apoptotic cascade: the exteriorization of phosphatidylserine using Annexin V, the caspase activation using FITC-VAD-FMK and the alteration of plasma membrane permeability employing YO-PRO-1. These assays were performed on control oocytes, oocytes exposed to vitrification solutions (toxicity control) and vitrified oocytes either immediately after warming or after incubation for 2h into maturation medium. The exposition to vitrification solutions triggered an increase of the percentage of oocytes both faintly (VAD+ PI-) and strongly (VAD++ PI-) labeled by FITC-VAD-FMK but not a significant modification of the number of oocytes Annexin V (A+ PI-, early apoptotic) and YO-PRO-1(YP+ PI-, apoptotic) positive in comparison with control oocytes. Oocytes submitted to the whole vitrification procedure showed a rise of the percentage of early apoptotic oocytes (A+ PI-) and FITC-VAD-FMK positive oocytes (VAD+/VAD++ PI-) and a contemporaneous increase of the number of dead oocytes (PI+). On the contrary, vitrified oocytes analyzed immediately after warming did not show a significant increase in the percentage of apoptotic oocytes (YO-PRO-1+/PI-) as compared with the control. Post warming incubation for 2h into maturation medium, in comparison with oocytes analyzed immediately after warming, did not induce any increase in the percentage of early apoptotic (A+ P-) oocytes while a decrease of the percentage of VAD+/PI- oocytes and a contemporaneous increase of VAD-/PI- oocytes were observed. Moreover, the post-warming incubation induced a rise of the percentage of apoptotic oocytes (YO-PRO-1+/PI-). All these data confirm the involvement of apoptotic mechanisms on the injuries induced by vitrification procedure in pig oocytes; explanation of this phenomenon could be useful to improve oocytes' cryopreservation protocols. Copyright 2012 Elsevier B.V
机译:卵母细胞和胚胎冷冻保存已成功应用于许多哺乳动物。然而,由于猪卵母细胞对冷冻损伤的敏感性更高,因此它们在体外受精的能力降低,并且发育能力也较低。这项研究的目的是评估冷冻冷冻方法卵化的猪卵母细胞的凋亡状态。我们评估了与凋亡级联反应激活有关的三个参数:使用膜联蛋白V的磷脂酰丝氨酸的外在化,使用FITC-VAD-FMK的胱天蛋白酶激活和使用YO-PRO-1改变质膜通透性。这些测定是在对照卵母细胞,暴露于玻璃化溶液的卵母细胞(毒性对照)和玻璃化的卵母细胞上进行的,这些实验是在加热后立即进行或在成熟培养基中孵育2小时后进行的。暴露于玻璃化溶液会触发FITC-VAD-FMK标记的微弱(VAD + PI-)和强(VAD ++ PI-)卵母细胞百分比的增加,但并未显着改变卵磷脂膜联蛋白V(A + PI- ,早期凋亡)和YO-PRO-1(YP + PI-,凋亡)与对照卵母细胞相比呈阳性。经历了整个玻璃化过程的卵母细胞显示出早期凋亡卵母细胞(A + PI-)和FITC-VAD-FMK阳性卵母细胞(VAD + / VAD ++ PI-)的百分比增加,而死亡卵母细胞数(PI +)同时增加。相反,在加热后立即分析的玻璃化卵母细胞与对照相比没有显示出凋亡卵母细胞百分比(YO-PRO-1 + / PI-)的显着增加。与在加热后立即分析的卵母细胞相比,在成熟培养基中温育2h后,不会诱导早期凋亡(A + P-)卵母细胞百分比的任何增加,而VAD + / PI-卵母细胞百分比的下降和同期观察到VAD- / PI-卵母细胞增加。此外,升温后的温育引起凋亡卵母细胞(YO-PRO-1 + / PI-)的百分比增加。所有这些数据证实了凋亡机制与猪卵母细胞玻璃化过程所致的损伤有关。这种现象的解释可能有助于改善卵母细胞的冷冻保存规程。版权所有2012 Elsevier B.V

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