绵羊胚胎在添加不同血清组分培养基中的体外发育。

P A Batt, B G Miller
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引用次数: 10

摘要

绵羊胚胎一般只能在体外添加血清或血清成分的培养基中发育成膨大囊胚。为了更好地了解血清对胚胎发育的支持作用,我们将一批羊血清通过(a)超滤分离成分子量大于10 Kd(千道尔)和小于10 Kd(千道尔)的两种成分,(b)凝胶过滤分离成蛋白质组分1、2和3,其中蛋白质基团的平均分子量分别约为500、150和65 Kd。分数3的主要蛋白质是白蛋白。将第6天的羊桑葚胚在碳酸氢钠缓冲盐溶液中体外培养48小时,盐溶液中添加不同浓度的羊血清或这些成分或血清的蛋白质部分。桑葚胚在添加全血清或只添加大于10 Kd组分和蛋白质组分3的培养基中可以发育为完全膨大的囊胚,而在添加小于10 Kd组分和蛋白质组分1或2的培养基中不能发育为完全膨大的囊胚。然而,在添加大于10 Kd成分或蛋白质组分3的培养基中,通过在培养基中添加小于10 Kd成分的血清,胚胎完全发育的比例增加。在含有蛋白组分3和小于10 Kd成分的培养基中,添加蛋白组分2可降低胚胎发育成膨大囊胚的比例,而在含有全血清的培养基中则无此作用。由于不同血清的成分可能有显著差异,这些结果表明(a)不同血清在体外支持胚胎发育的能力不同的原因,以及(b)可能影响子宫内绵羊胚胎发育的因素,其中血浆蛋白几乎包含胚胎液体中的所有蛋白质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of sheep embryos in vitro in a medium supplemented with different serum fractions.

Sheep embryos will generally develop into expanded blastocysts in vitro only in culture media supplemented with serum or serum components. In order to better understand how serum supports embryo development, a batch of ovine serum was fractionated by (a) ultrafiltration into two components containing substances with molecular weights greater and less than 10 Kd (kilodaltons), and (b) gel filtration into protein fractions 1, 2 and 3, containing groups of proteins with mean molecular weights of about 500, 150 and 65 Kd, respectively. The principal protein in fraction 3 was albumin. Day 6 sheep morulae were cultured in vitro for 48 hours in a bicarbonate-buffered salt solution supplemented with various concentrations of ovine serum or of these components or protein fractions of serum. Morulae could develop to fully expanded blastocysts in medium supplemented with whole serum or with the greater than 10 Kd component or protein fraction 3 only, but could not develop in medium supplemented with the less than 10 Kd component only or with the less than 10 Kd component and protein fractions 1 or 2. However, the proportion of embryos that developed fully in medium supplemented with the greater than 10 Kd component or protein fraction 3 was increased by adding the less than 10 Kd component of serum to the medium. The addition of protein fraction 2 decreased the proportion of embryos that developed to expanded blastocysts in medium containing protein fraction 3 and the less than 10 Kd component, but not in medium containing whole serum. Since the compositions of different sera may vary markedly, these results suggest (a) reasons why different sera vary in their ability to support embryo development in vitro, and (b) factors which may influence development of the sheep embryo in the uterus, where plasma proteins comprise nearly all the protein in the fluid bathing the embryo.

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