What knockout mice can tell us about parturition.

T Kimura, K Ogita, C Kusui, K Ohashi, C Azuma, Y Murata
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引用次数: 42

Abstract

Many molecules, including steroid and peptide hormones, prostaglandins and cytokines, regulate the preparation, initiation and progression of parturition in mammals. Gene targeting studies show that, in the knockout mice of steroid 5alpha-reductase type 1 gene, prostaglandin F2alpha receptor gene and cytosolic phospholipase A2 gene, parturition was severely disturbed, although live offspring were delivered by Caesarean section. Relaxin gene-disrupted mice also showed protracted labour. However, most knockout mice in which the steroid hormone, prostaglandin, cytokine or peptide hormone (for example, oxytocin, corticotrophin releasing hormone and endothelin) endocrine-paracrine systems are disrupted are inadequate for analysis of the mechanism of parturition because they die before reaching reproductive age or are infertile, or because they reproduce normally. A conditional knockout strategy, for example, using the Cre-LoxP system, should be considered for investigating the biochemical background of parturition to overcome these problems.

敲除小鼠能告诉我们的关于分娩的信息。
许多分子,包括类固醇和肽激素、前列腺素和细胞因子,调节哺乳动物分娩的准备、开始和进展。基因靶向研究表明,在类固醇5 α -还原酶1型基因、前列腺素f2 α受体基因和胞质磷脂酶A2基因敲除小鼠中,尽管通过剖宫产产下了存活的后代,但分娩受到严重干扰。松弛素基因被破坏的小鼠也表现出分娩延迟。然而,大多数敲除小鼠体内的类固醇激素、前列腺素、细胞因子或肽激素(如催产素、促肾上腺皮质激素释放激素和内皮素)内分泌-旁分泌系统被破坏,因为它们在达到育龄前死亡或不育,或因为它们正常繁殖,因此不足以分析分娩机制。为了克服这些问题,应该考虑采用条件敲除策略,例如使用Cre-LoxP系统来研究分娩的生化背景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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