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Progress in reproductive biotechnology in swine

机译:猪生殖生物技术的进展

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This article summarizes recent progress in reproductive biotechnology in swine with special reference to in vitro production of embryos, generation of identical multiples, and transgenic pigs useful for xenotransplantation. In vitro production (in vitro maturation, in vitro fertilization, and in vitro culture) of viable porcine embryos is possible, although with much lower success rates than in cattle. The main problems are insufficient cytoplasmic maturation of porcine oocytes, a high proportion of polyspermic fertilization and a low proportion of blastocysts that, in addition, are characterized by a low number of cells, hampering their development in vivo upon transfer to recipients. Microsurgical bisection of morula and blastocyst stage embryos leads to a 2 to 3% monozygotic twinning rate of the transferred demiembryos, which is similar to that in rabbits and mice but considerably lower than in ruminants. It was found that with decreasing quality an increasing proportion of demi-embryos did not possess an inner cell mass. Porcine individual blastomeres derived from 4- and 8-cell embryos can be cultured in defined medium to the blastocyst stage. Leukemia inhibitory factor has been shown to be effective at defined embryonic stages and supports the formation of the inner cell mass in cultured isolated blastomeres in a concentration-dependent manner. For maintaining pregnancies with micromanipulated porcine embryos, it is not necessary to transfer extraordinarily high numbers of embryos. Porcine nuclear transfer is still struggling from the inefficiency of producing normally functioning blastocysts. Blastomeres, blastocyst-derived cells, fibroblasts and granulosa cells have been employed as donor cells in porcine nuclear transfer and have yielded blastocysts. Recently, the generation of the first piglets from somatic cell nuclear transfer has been achieved. DNA-microinjection into pronuclei of porcine zygotes has reliably resulted in the generation of transgenic pigs, which have special importance for the production of valuable pharmaceutical proteins in milk and xenotransplantation. It has been demonstrated that by expression of human complement regulatory proteins in transgenic pigs the hyperacute rejection response occurring after xenotransplantation can be overcome in a clinically relevant manner. Although biotechnological procedures in swine have recently undergone tremendous progress, the development is still tagging behind that in cattle and sheep. With regard to genetic engineering, considerable progress will originate from the possibility of employing homologous recombination in somatic cell lines and their subsequent use in nuclear transfer. In combination with the increasing knowledge in gene sequences this will allow in the foreseeable future widespread use in the pig industry either for agricultural or biomedical purposes.
机译:本文总结了猪生殖生物技术的最新进展,特别是涉及胚胎的体外生产,相同倍数的产生以及可用于异种移植的转基因猪。可行的猪胚胎的体外生产(体外成熟,体外受精和体外培养)是可能的,尽管成功率远低于牛。主要问题是猪卵母细胞的细胞质成熟不足,多精子受精的比例高和胚泡的比例低,此外,其特征在于细胞数量少,阻碍了它们在体内转移至受体后的发育。桑ula和胚泡期胚胎的显微外科分割导致转移的成胚细胞的2至3%单卵双胞胎孪生率,这与兔子和小鼠相似,但比反刍动物低得多。发现随着质量下降,半胚的比例增加而没有内部细胞团。可以将来自4细胞和8细胞胚胎的猪单个卵裂球在确定的培养基中培养至胚泡期。白血病抑制因子已显示在确定的胚胎阶段有效,并以浓度依赖的方式支持培养的分离卵裂球内细胞团的形成。为了维持显微操作的猪胚胎的怀孕,没有必要转移数量过多的胚胎。由于产生正常功能的胚泡的效率低下,猪核移植仍在努力中。在猪的核转移中,卵裂球,胚泡来源的细胞,成纤维细胞和颗粒细胞已被用作供体细胞,并产生了胚泡。最近,已经实现了从体细胞核移植产生第一批仔猪。将DNA显微注射到猪受精卵的原核中已可靠地导致了转基因猪的产生,这对于在牛奶和异种移植中生产有价值的药物蛋白具有特别重要的意义。已经证明,通过在转基因猪中表达人补体调节蛋白,可以以临床相关的方式克服异种移植后发生的超急性排斥反应。尽管猪的生物技术程序最近取得了巨大进展,但其发展仍落后于牛和羊。关于基因工程,相当大的进展将源于在体细胞系中采用同源重组及其在核移植中的后续应用的可能性。结合对基因序列知识的不断增长,这将在可预见的将来允许其在养猪业中广泛用于农业或生物医学目的。

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