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人类子宫内膜在月经周期中产生的内皮细胞迁移信号。

Endothelial cell migratory signal produced by human endometrium during the menstrual cycle.

作者信息

Rogers P A, Abberton K M, Susil B

机构信息

Department of Obstetrics and Gynaecology, Monash University, Clayton, Victoria, Australia.

出版信息

Hum Reprod. 1992 Sep;7(8):1061-6. doi: 10.1093/oxfordjournals.humrep.a137793.

Abstract

Human endometrial explants were cultured in a three-dimensional collagen/bovine aortic endothelial cell (BAEC) matrix to measure angiogenic activity, as represented by migration of BAEC towards the explants. The 57 endometrial biopsies were classified by histological appearance into nine stages of the menstrual cycle; five proliferative groupings, three secretory groupings and one menstrual. The BAEC migratory score was taken as the average for 12 explants assayed from each biopsy. The results showed two significant peaks of BAEC migratory activity, one during the early proliferative phase and one during the mid--late proliferative phase. There was a significant drop in the BAEC migratory signal from early--mid-proliferative endometrial explants compared to most other stages of the cycle. The results also show a non-significant rise in BAEC migratory activity in the mid-secretory phase of the cycle. Overall, the results support the concept of two or three different endometrial angiogenic events during the human menstrual cycle, a post-menstrual repair, a mid--late proliferative growth and a lesser mid-secretory activity that may be associated with spiral arteriole growth. Each of these events occurs under different hormonal environments and will need to be investigated separately in terms of local mechanisms controlling angiogenesis.

摘要

将人子宫内膜外植体培养在三维胶原蛋白/牛主动脉内皮细胞(BAEC)基质中,以测量血管生成活性,该活性通过BAEC向外植体的迁移来表示。57份子宫内膜活检标本根据组织学外观被分为月经周期的九个阶段:五个增殖期分组、三个分泌期分组和一个月经期分组。BAEC迁移评分取每个活检标本检测的12个外植体的平均值。结果显示BAEC迁移活性有两个显著峰值,一个在增殖早期,另一个在增殖中晚期。与月经周期的大多数其他阶段相比,增殖早期至中期子宫内膜外植体的BAEC迁移信号显著下降。结果还显示,在月经周期的分泌中期,BAEC迁移活性有不显著的升高。总体而言,这些结果支持了人类月经周期中存在两到三种不同的子宫内膜血管生成事件的概念,即月经后修复、增殖中晚期生长以及可能与螺旋小动脉生长相关的分泌中期较弱的活性。这些事件中的每一个都发生在不同的激素环境下,需要分别从控制血管生成的局部机制方面进行研究。

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