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高效的一步法直接转移到在体外培养和化学定义的培养基中冷冻的解冻牛胚胎的受体。

Efficient one-step direct transfer to recipients of thawed bovine embryos cultured in vitro and frozen in chemically defined medium.

机构信息

Centro de Biotecnología Animal-SERIDA, Camino de Rioseco 1225, Gijón, 33394, Spain.

Centro de Biotecnología Animal-SERIDA, Camino de Rioseco 1225, Gijón, 33394, Spain.

出版信息

Theriogenology. 2020 Apr 1;146:39-47. doi: 10.1016/j.theriogenology.2020.01.056. Epub 2020 Feb 1.

Abstract

Direct transfer (DT) of cryopreserved embryos to recipients facilitates on-farm application. We analyzed a new freezing/thawing (F/T) procedure for in vitro produced (IVP) embryos, integrating: 1) an ethylene-glycol based system; 2) a culture step without protein; and 3) a synthetic protein substitute (CRYO3) in cryopreservation medium. IVP embryos from abattoir ovaries were cultured in groups in BSA-containing synthetic oviduct fluid with or without 0.1% fetal calf serum (FCS) until Day-6. Morulae and early blastocysts were subsequently cultured without protein from Day-6 onwards. Day 7 and Day 8 expanded blastocysts (EXB) were subjected to F/T or vitrification/warming (V/W). Thawed and warmed EXB were cultured in vitro, and development rates, cell counts and dead cells were analyzed in surviving embryos. V/W improved survival over F/T (live and hatching rates at 2 h, 24 h and 48 h) (P < 0.0001), and FCS before Day 6 did not affect in vitro survival. After F/T, embryos had lower cell counts in the ICM, TE and total cells than after V/W. Day-7 embryos after F/T showed % apoptotic, % pycnotic and % total dead cells higher (p < 0.05) than their Day-8 counterparts, probably because F/T reduced the numbers of ICM cells within Day-8 embryos. Thereafter, Day-7 blastocysts were transferred to heifers in an experimental herd. There were no differences in birth rates with frozen (-FCS [n = 40]: 45%; +FCS [n = 14]: 28%), vitrified (-FCS [n = 47]: 53%; +FCS [n = 11]: 36%) and fresh (-FCS [n = 30]: 47%; +FCS [n = 17]: 53%) embryos. However, frozen embryos produced with FCS showed 5/9 miscarriages after Day-40. Calves born from frozen (n = 22), vitrified (n = 29) and fresh (n = 22) transfers did not differ in birth weight, gestation length and daily gain weight (P > 0.10). Subsequently, transfer of frozen embryos (n = 29) derived from oocytes collected from live, hormonally stimulated cows in experimental herd, led to pregnancy rates of 57% (heifers) and 40% (dry cows). with EXB on Day-62 Finally, embryos produced with BSA were transferred to cows in an on-field trial (frozen [n = 80]; fresh [n = 58]), with no differences in pregnancy rates (days 30-40). Pregnancy and birth rates could not be predicted from in vitro approaches. The new F/T system yields pregnancy and birth rates comparable to vitrified and fresh embryos without birth overweight. The absence of products of animal origin, defined chemical composition, and direct transfer entail sanitary, manufacturing and application advantages.

摘要

直接将冷冻胚胎转移给受体有利于农场应用。我们分析了一种新的 IVP 胚胎冷冻/解冻(F/T)程序,包括:1)基于乙二醇的系统;2)无蛋白质的培养步骤;3)在冷冻保护剂中使用合成蛋白替代物(CRYO3)。屠宰场卵巢的 IVP 胚胎在含有 BSA 的合成输卵管液中分组培养,有或没有 0.1%胎牛血清(FCS),直到第 6 天。第 6 天以后,将桑葚胚和早期囊胚在无蛋白质的情况下继续培养。第 7 天和第 8 天的扩张囊胚(EXB)进行 F/T 或玻璃化/解冻(V/W)。解冻和变暖的 EXB 在体外培养,并分析存活胚胎的发育率、细胞计数和死亡细胞。V/W 提高了 F/T 的存活率(2 小时、24 小时和 48 小时的活产率和孵化率)(P < 0.0001),第 6 天之前的 FCS 不影响体外存活率。F/T 后,胚胎的 ICM、TE 和总细胞计数均低于 V/W。F/T 后第 7 天的胚胎显示凋亡百分比、固缩百分比和总死亡细胞百分比较高(p < 0.05),可能是因为 F/T 减少了第 8 天胚胎中 ICM 细胞的数量。此后,第 7 天的囊胚被转移到实验牛群中的奶牛。冷冻(-FCS [n = 40]:45%;+FCS [n = 14]:28%)、玻璃化(-FCS [n = 47]:53%;+FCS [n = 11]:36%)和新鲜(-FCS [n = 30]:47%;+FCS [n = 17]:53%)胚胎的产犊率没有差异。然而,用 FCS 产生的冷冻胚胎在第 40 天后出现 5/9 例流产。来自冷冻(n = 22)、玻璃化(n = 29)和新鲜(n = 22)移植的犊牛在出生体重、妊娠期和日增重方面没有差异(P > 0.10)。随后,从实验牛群中活体、激素刺激的奶牛采集的卵母细胞中转移冷冻胚胎(n = 29),导致受孕率为 57%(小母牛)和 40%(干奶牛)。最后,在现场试验中(冷冻[n = 80];新鲜[n = 58]),用 BSA 生产的胚胎被转移到奶牛身上,妊娠率没有差异(30-40 天)。妊娠和产犊率不能从体外方法预测。新的 F/T 系统产生的妊娠和产犊率与玻璃化和新鲜胚胎相当,没有出生超重。没有动物源性产品、明确的化学成分和直接转移,具有卫生、制造和应用优势。

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