Suppr超能文献

一种与延迟着床相关的蛋白质可在体外阻止延迟着床小鼠囊胚的滋养外胚层恢复DNA合成。

A delayed-implantation-associated protein prevents resumption of DNA synthesis by the trophectoderm of delayed-implanting mouse blastocysts in vitro.

作者信息

Katagiri S, Takahashi Y, Kanagawa H, Yuen B H, Moon Y S

机构信息

Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.

出版信息

J Vet Med Sci. 1998 Jul;60(7):791-4. doi: 10.1292/jvms.60.791.

Abstract

Objective of this study was to determine the ability of a delayed-implantation-associated protein (MW 170,000, DIAP170K) to inhibit DNA synthesis by mouse blastocysts. Mice were ovariectomized on day 3 of pregnancy and treated with daily injections with 1 mg progesterone till day 7 to induce delayed implantation. Blastocysts were collected on day 8 with or without a single injection of 25 ng estradiol-17 beta on day 7 that activates blastocyst metabolisms (activated blastocysts and delayed-implanting blastocysts respectively). DNA synthesis was determined by measuring [3H]thymidine incorporation by blastocysts. DIAP170K at 10 micrograms/m/ suppressed resumption of DNA synthesis by delayed-implanting blastocysts and suppression was maximal at 50 micrograms/m/. However, DIAP170K did not affect DNA synthesis by blastocysts obtained on day 5 of pregnancy (normal blastocysts) and activated blastocysts. Resumption of DNA synthesis in the inner cell mass (ICM) and trophectoderm from delayed-implanting blastocysts was then separately assessed. DNA synthesis resumed in the trophectoderm of intact blastocysts during 24-hr culture but not in the trophectoderm cultured apart from the ICM. DIAP170K inhibited the resumption of DNA synthesis by the trophectoderm of intact delayed-implanting blastocysts but did not affect DNA synthesis by the ICM. In conclusion, DIAP170K inhibits resumption of DNA synthesis by trophectoderm of delayed-implanting blastocysts. This action of DIAP170K may play a central role in maintaining, but not achieving, dormancy of DNA synthesis by delayed-implanting blastocysts in mice.

摘要

本研究的目的是确定一种与延迟着床相关的蛋白质(分子量170,000,DIAP170K)抑制小鼠囊胚DNA合成的能力。在妊娠第3天对小鼠进行卵巢切除,并每日注射1 mg孕酮直至第7天以诱导延迟着床。在第8天收集囊胚,其中一组在第7天单次注射25 ng雌二醇-17β以激活囊胚代谢(分别为激活的囊胚和延迟着床的囊胚)。通过测量囊胚对[3H]胸腺嘧啶核苷的掺入来确定DNA合成。10微克/毫升的DIAP170K可抑制延迟着床囊胚DNA合成的恢复,在50微克/毫升时抑制作用最大。然而,DIAP170K并不影响妊娠第5天获得的囊胚(正常囊胚)和激活的囊胚的DNA合成。然后分别评估延迟着床囊胚内细胞团(ICM)和滋养外胚层中DNA合成的恢复情况。完整囊胚的滋养外胚层在24小时培养期间恢复了DNA合成,但与ICM分离培养的滋养外胚层则未恢复。DIAP170K抑制完整的延迟着床囊胚滋养外胚层DNA合成的恢复,但不影响ICM的DNA合成。总之,DIAP170K抑制延迟着床囊胚滋养外胚层DNA合成的恢复。DIAP170K的这一作用可能在维持小鼠延迟着床囊胚DNA合成的休眠状态(而非实现休眠)中起核心作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验