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原癌基因c-ets 1和尿激酶型纤溶酶原激活剂在小鼠着床和胎盘形成过程中的作用。

Involvement of the proto-oncogene c-ets 1 and the urokinase plasminogen activator during mouse implantation and placentation.

作者信息

Grevin D, Chen J H, Raes M B, Stehelin D, Vandenbunder B, Desbiens X

机构信息

Laboratoire d'Oncologie Moléculaire, CNRS URA 1160, Institut Pasteur, Lille, France.

出版信息

Int J Dev Biol. 1993 Dec;37(4):519-29.

PMID:8179996
Abstract

Many of the Ets proteins have been shown to be transcription activators. In vitro, Ets 1 proteins are involved in the transcriptional induction of genes such as stromelysin 1, collagenase 1 or urokinase type plasminogen activator, which are proteases responsible for extracellular matrix degradation. In vivo, c-ets 1 is expressed in a wide variety of embryonic tissues in migrating cells, especially in endothelial cells during blood vessel formation. C-ets 1 is also expressed in stromal cells of invasive carcinomas. In the present work, we have investigated the expression of both c-ets 1 and u-PA, a putative target gene of the Ets 1 proteins, within a biological model which includes both embryonic and tumoral aspects. Implantation and placentation of the mouse embryo display migration of the trophoblastic cells, which invade the stroma of the uterine endometrium and trigger the establishment of a new vascular frame. Using in situ hybridization, we show that the overlapping of expression of c-ets 1 and u-PA is restricted to some maternal cell populations from the invasive front and to the endothelial cells of the endometrial vasculature. C-ets 1 is never expressed in trophoblasts. In contrast, u-PA expression in trophoblasts is strong and coincides with the embryo invasive phase. In the embryo proper, c-ets 1 displays a spatio-temporal expression pattern similar to that described in the chick embryo. Until E 10.5, u-PA is expressed neither in embryonic nor in extra-embryonic structures. The respective roles of c-ets 1 and u-PA and their relationship during mammalian placentation are discussed.

摘要

许多Ets蛋白已被证明是转录激活因子。在体外,Ets 1蛋白参与诸如基质溶解素1、胶原酶1或尿激酶型纤溶酶原激活剂等基因的转录诱导,这些都是负责细胞外基质降解的蛋白酶。在体内,c-ets 1在迁移细胞的多种胚胎组织中表达,尤其是在血管形成过程中的内皮细胞中。c-ets 1也在浸润性癌的基质细胞中表达。在本研究中,我们在一个包含胚胎和肿瘤两方面的生物学模型中,研究了c-ets 1和u-PA(Ets 1蛋白的一个假定靶基因)的表达情况。小鼠胚胎的着床和胎盘形成过程中,滋养层细胞会发生迁移,这些细胞侵入子宫内膜的基质并触发新血管框架的建立。通过原位杂交,我们发现c-ets 1和u-PA的表达重叠仅限于侵入前沿的一些母体细胞群体以及子宫内膜脉管系统的内皮细胞。c-ets 1在滋养层细胞中从未表达。相反,滋养层细胞中u-PA的表达很强,且与胚胎侵入期一致。在胚胎本身,c-ets 1呈现出与鸡胚中描述的类似的时空表达模式。直到胚胎发育第10.5天,u-PA在胚胎结构和胚外结构中均未表达。本文讨论了c-ets 1和u-PA在哺乳动物胎盘形成过程中的各自作用及其关系。

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