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蜕膜化对大鼠子宫内膜中bax和bcl-2表达的影响。

Effect of decidualization on the expression of bax and bcl-2 in the rat uterine endometrium.

作者信息

Akcali K C, Khan S A, Moulton B C

机构信息

Department of Cell Biology, University of Cincinnati College of Medicine, Ohio 45267-0526, USA. 526, USA.

出版信息

Endocrinology. 1996 Jul;137(7):3123-31. doi: 10.1210/endo.137.7.8770938.

Abstract

During early pregnancy, the uterine endometrium responds to an implanting blastocyst with the extensive growth and differentiation of decidualization. This transformation of endometrial stromal cells begins in the antimesometrial side of the uterus to form a primary decidual zone, expands to form a secondary zone in the antimesometrium, and eventually transforms stromal cells in the mesometrial region. During pregnancy, both decidual zones regress by apoptosis, leaving decidual cells in the mesometrial region to form decidua basalis and the mature placenta. Molecular mechanisms controlling cell death during blastocyst implantation and decidualization are unknown. We examined the hypothesis that progesterone and estrogen control of endometrial differentiation and eventual apoptosis involves control of bcl-2 gene family expression. Ovariectomized rats were primed with estradiol and treated with progestin (medroxyprogesterone acetate, 3.5 mg) and estradiol (200 ng) before an intrauterine stimulus to initiate decidualization. Expression of the two bax messenger RNA transcripts, 1.0 and 1.5 kilobases, was examined by Northern blot analysis after hormone treatment and decidualization, and only the 1.0-kilobase transcript was induced. After the same treatments, the expression of bcl-2, a suppressor of apoptosis, decreased. In situ analysis revealed a cell type-specific increase in bax expression after the hormonal treatment and decidualization. This increase was first seen in luminal and glandular epithelial cells and then in the periluminal stroma 24 h after intrauterine stimulation, with eventual progressive expression throughout the stroma. Expression of bcl-2 decreased after hormone treatment and decidualization. Immunohistochemical studies of Bax showed that expression of Bax protein accompanied decidualization of the stroma. Bcl-2 protein was only seen in the luminal and glandular epithelia, and its level decreased as decidualization progressed. These data indicate that the balance between bax and bcl-2 expression is altered during stromal cell differentiation. Increased expression of bax precedes nucleosomal DNA fragmentation and eventual apoptosis, which plays a significant role in placental development.

摘要

在妊娠早期,子宫内膜对植入的囊胚作出反应,发生广泛的蜕膜化生长和分化。子宫内膜基质细胞的这种转变始于子宫的反系膜侧,形成一个初级蜕膜区,扩展至反系膜中形成一个次级区,最终使系膜区的基质细胞发生转变。在怀孕期间,两个蜕膜区通过凋亡而退化,在系膜区留下蜕膜细胞以形成基蜕膜和成熟胎盘。囊胚植入和蜕膜化过程中控制细胞死亡的分子机制尚不清楚。我们检验了以下假说:孕酮和雌激素对子宫内膜分化及最终凋亡的控制涉及对bcl-2基因家族表达的控制。对去卵巢大鼠用雌二醇进行预处理,并在子宫内刺激以启动蜕膜化之前,用孕激素(醋酸甲羟孕酮,3.5毫克)和雌二醇(200纳克)进行处理。在激素处理和蜕膜化后,通过Northern印迹分析检测两种bax信使核糖核酸转录本(1.0和1.5千碱基)的表达,结果仅诱导出1.0千碱基的转录本。经过相同处理后,凋亡抑制因子bcl-2的表达下降。原位分析显示,在激素处理和蜕膜化后,bax表达出现细胞类型特异性增加。这种增加首先在腔上皮细胞和腺上皮细胞中出现,然后在子宫内刺激后24小时在腔周基质中出现,最终在整个基质中逐渐表达。激素处理和蜕膜化后,bcl-2的表达下降。对Bax的免疫组织化学研究表明,Bax蛋白的表达伴随着基质的蜕膜化。Bcl-2蛋白仅见于腔上皮细胞和腺上皮细胞,并且随着蜕膜化的进展其水平下降。这些数据表明,在基质细胞分化过程中,bax和bcl-2表达之间的平衡发生了改变。bax表达的增加先于核小体DNA片段化和最终的凋亡,这在胎盘发育中起重要作用。

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