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大鼠胚胎植入前后子宫内皮细胞的增殖情况

Uterine endothelial cell proliferation before and after embryo implantation in rats.

作者信息

Goodger A M, Rogers P A

机构信息

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

出版信息

J Reprod Fertil. 1993 Nov;99(2):451-7. doi: 10.1530/jrf.0.0990451.

Abstract

Angiogenesis occurs rarely in normal adult tissues. The female reproductive tract, however, provides several exceptions, including the endometrium during early pregnancy. The aim of this study was to quantify endothelial cell proliferation (a component of angiogenesis) in the rat endometrium at about the time of implantation, using immunohistochemistry with a double staining technique. Proliferating cells were stained using an antibody against proliferating cell nuclear antigen (PCNA; clone PC10), and endothelial cells were stained with a lectin from Griffonia simplicifolia. Results showed that the endothelial cell proliferative index in the endometrium rose significantly from approximately 1% on the first 2 days of pregnancy to 13% on day 3; and continued to rise to 28% on day 5. After embryo implantation, the endometrial endothelial cell proliferative index rose further to 71% on day 7 at embryo sites only; but significantly decreased to basal values at intersites. The endothelial cell proliferative indices in the myometrium and mesometrial triangle remained at basal values during the first 5 days, but increased to approximately 22% at embryo sites only by day 7. We conclude that in the rat: (1) endometrial angiogenesis may be occurring before embryo implantation; (2) endometrial endothelial and stromal cell proliferation occurs concomitantly, except on day 3 when endothelial cell proliferation begins in advance of other stromal cell proliferation; and (3) there are two separate mechanisms controlling uterine endothelial cell proliferation during early pregnancy. The first mechanism is maternally controlled and is apparent throughout the entire endometrium from day 3; and the second mechanism is apparent after implantation in the vicinity of the embryo.

摘要

血管生成在正常成年组织中很少发生。然而,女性生殖道是几个例外情况之一,包括妊娠早期的子宫内膜。本研究的目的是使用双重染色技术的免疫组织化学方法,在植入时对大鼠子宫内膜中的内皮细胞增殖(血管生成的一个组成部分)进行定量。使用抗增殖细胞核抗原(PCNA;克隆PC10)的抗体对增殖细胞进行染色,并用来自西非豆的凝集素对内皮细胞进行染色。结果显示,子宫内膜中的内皮细胞增殖指数从妊娠第1至2天的约1%显著上升至第3天的13%;并在第5天继续上升至28%。胚胎植入后,仅在胚胎着床部位,子宫内膜内皮细胞增殖指数在第7天进一步上升至71%;但在非着床部位显著降至基础值。子宫肌层和阔韧带三角区的内皮细胞增殖指数在最初5天保持在基础值,但到第7天仅在胚胎着床部位增加到约22%。我们得出结论,在大鼠中:(1)子宫内膜血管生成可能在胚胎植入前就已发生;(2)子宫内膜内皮细胞和基质细胞增殖同时发生,但在第3天除外,此时内皮细胞增殖先于其他基质细胞增殖开始;(3)在妊娠早期有两种独立的机制控制子宫内皮细胞增殖。第一种机制由母体控制,从第3天起在整个子宫内膜中都很明显;第二种机制在胚胎植入后在胚胎附近很明显。

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