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狒狒(埃及狒狒)子宫内膜对雌激素和孕激素依赖性蛋白的合成与释放

Synthesis and release of estrogen- and progesterone-dependent proteins by the baboon (Papio anubis) uterine endometrium.

作者信息

Fazleabas A T, Miller J B, Verhage H G

机构信息

Department of Obstetrics and Gynecology, University of Illinois, College of Medicine, Chicago 60680.

出版信息

Biol Reprod. 1988 Oct;39(3):729-36. doi: 10.1095/biolreprod39.3.729.

Abstract

This study was undertaken to determine the regulation of stage-specific endometrial proteins of the baboon uterus by estradiol (E2) and progesterone (P). Ovariectomized females were either untreated or treated with E2 for 7 or 14 days, or primed with E2 for 14 days, and then treated with E2 plus P or P alone for 7 or 14 days. Steroids were administered via Silastic capsules and, as determined by radioimmunoassay, physiological levels were present in the peripheral serum of each treatment group. Endometrial tissue obtained after steroid treatment was incubated in the presence of [35S]methionine for 24 h at 37 degrees C, and the culture medium was analyzed by two-dimensional polyacrylamide gel electrophoresis (2-D PAGE) followed by fluorography. Steroid treatment resulted in a doubling of the synthesis and release of labeled macromolecules into culture medium compared to the levels observed in long-term ovariectomized animals, together with the appearance of specific proteins whose synthesis required either E2 or E2 +/- P. A single protein (Mr 33,000; pI 7.6) was only observed after E2 treatment, and a family of high molecular weight basic proteins (Mr greater than 200,000) and a group of acidic proteins (Mr 130,000) required both E2 and P. In the absence of E2, P maintained the synthesis and release of three basic proteins (Mr 88,000, 66,000, and 40,000) as well as the other proteins observed in the ovariectomized animals.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究旨在确定雌二醇(E2)和孕酮(P)对狒狒子宫阶段特异性子宫内膜蛋白的调节作用。对去卵巢的雌性动物,一组不进行处理,其余分别用E2处理7天或14天,或先用E2预处理14天,然后再用E2加P或单独用P处理7天或14天。类固醇通过硅橡胶胶囊给药,通过放射免疫测定法测定,各治疗组外周血清中均存在生理水平的类固醇。类固醇处理后获得的子宫内膜组织在含有[35S]甲硫氨酸的条件下于37℃孵育24小时,然后通过二维聚丙烯酰胺凝胶电泳(2-D PAGE)和荧光自显影分析培养基。与长期去卵巢动物相比,类固醇处理使标记大分子的合成和释放增加了一倍,同时出现了合成需要E2或E2 +/- P的特定蛋白质。仅在E2处理后观察到一种单一蛋白质(分子量33,000;等电点7.6),一组高分子量碱性蛋白质(分子量大于200,000)和一组酸性蛋白质(分子量130,000)的合成需要E2和P两者。在没有E2的情况下,P维持了三种碱性蛋白质(分子量88,000、66,000和40,000)以及去卵巢动物中观察到的其他蛋白质的合成和释放。(摘要截短于250字)

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