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胰岛素可增加体外培养的小鼠植入前胚胎的细胞数量并促进其形态发育。

Insulin increases cell numbers and morphological development in mouse pre-implantation embryos in vitro.

作者信息

Gardner H G, Kaye P L

机构信息

Department of Physiology and Pharmacology, University of Queensland, Australia.

出版信息

Reprod Fertil Dev. 1991;3(1):79-91. doi: 10.1071/rd9910079.

Abstract

Insulin, alone or in combination with bovine serum albumin (BSA), was investigated for its effects on cell proliferation and on the proportions of mouse pre-implantation embryos reaching compaction and forming blastocysts during culture in a common basal medium in vitro. Insulin promoted cleavage by 16-20% when added to medium for culture of 2-cell embryos to morulae, blastocysts and expanded blastocysts over 24, 48 and 72 h. These effects on cell division were supported by increases of 65-100% and 31-100% in the rates of compaction and blastocyst formation respectively. The results indicate that the receptor responsible for these actions is probably expressed prior to compaction and possibly at the 4-cell stage. Identical responses to 1.7 and 170 nM insulin suggest that the insulin receptor is capable of mediating both of these developmental effects, although similar mediation by an insulin-like growth factor-1 (IGF-1) receptor is not excluded. BSA, normally a component of culture media, promoted cleavage between 24 and 48 h of culture as well as compaction and blastocyst formation at 15 microM (1 g L-1), probably through nutritional support. Compaction appeared to be promoted by some non-specific action of BSA. Blastocysts that had developed in the presence of both 170 nM insulin and 15 microM BSA contained similar numbers of cells to blastocysts that had developed in vivo.

摘要

研究了胰岛素单独或与牛血清白蛋白(BSA)联合使用时,对细胞增殖以及体外培养于普通基础培养基中的小鼠植入前胚胎达到致密化和形成囊胚的比例的影响。当将胰岛素添加到用于2细胞胚胎培养至桑椹胚、囊胚和扩张囊胚的培养基中,在24、48和72小时培养期间,胰岛素使卵裂率提高了16%-20%。致密化率和囊胚形成率分别提高65%-100%和31%-100%,支持了这些对细胞分裂的作用。结果表明,负责这些作用的受体可能在致密化之前表达,可能在4细胞期表达。对1.7 nM和170 nM胰岛素的相同反应表明,胰岛素受体能够介导这两种发育效应,尽管不排除胰岛素样生长因子-1(IGF-1)受体有类似介导作用。BSA通常是培养基的一种成分,在15 μM(1 g/L)时,在培养24至48小时期间促进卵裂以及致密化和囊胚形成,可能是通过营养支持。致密化似乎是由BSA的一些非特异性作用促进的。在170 nM胰岛素和15 μM BSA存在下发育的囊胚所含细胞数量与体内发育的囊胚相似。

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