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早期滋养层细胞发育过程中蛋白酶激活受体(PARs)的表达模式。

The pattern of expression of protease-activated receptors (PARs) during early trophoblast development.

作者信息

Even-Ram Sharona Cohen, Grisaru-Granovsky Sorina, Pruss Diana, Maoz Miriam, Salah Zaidoun, Yong-Jun Yin, Bar-Shavit Rachel

机构信息

Department of Oncology, Pathology, Hadassah University Hospital, Jerusalem, Israel.

出版信息

J Pathol. 2003 May;200(1):47-52. doi: 10.1002/path.1338.

Abstract

Human fetal development depends on the ability of the embryo to gain access to the maternal circulation. Thus, specialized stem cells of the newly formed placenta, trophoblast, invade the uterus and its arterial network to establish an efficient feto-maternal molecular exchange. To accomplish this task, trophoblast differentiation during the first trimester of pregnancy involves cell proliferation, invasion, and extracellular matrix (ECM) remodelling. Trophoblast invasion shares many features with tumour cell invasion, with the distinction that it is strictly spatially and temporally controlled. We have previously demonstrated that PAR1, the first member of the protease-activated receptor (PAR) family, plays a central role in tumour cell invasion. In the present study we have examined the pattern of expression of PAR1 and other PAR family candidates during early human placental development. We show that PAR1 and PAR3 are highly and spatially expressed between the 7th and 10th weeks of gestation but not at the 12th week and thereafter. Likewise, high expression levels of PAR1 and PAR3 were observed in the cytotrophoblast cells of complete hydatidiform mole as compared to minimal levels in normal age-matched placenta. Together, our data suggest the involvement of PAR1 and PAR3 in restricted and unrestricted pathological trophoblast invasion.

摘要

人类胎儿发育依赖于胚胎进入母体循环的能力。因此,新形成的胎盘的特化干细胞——滋养层细胞,侵入子宫及其动脉网络,以建立高效的胎儿-母体分子交换。为完成此任务,妊娠头三个月期间的滋养层细胞分化涉及细胞增殖、侵袭和细胞外基质(ECM)重塑。滋养层细胞侵袭与肿瘤细胞侵袭有许多共同特征,区别在于它受到严格的空间和时间控制。我们之前已经证明,蛋白酶激活受体(PAR)家族的首个成员PAR1在肿瘤细胞侵袭中起核心作用。在本研究中,我们检测了PAR1和其他PAR家族候选成员在人类胎盘早期发育过程中的表达模式。我们发现,PAR1和PAR3在妊娠第7至10周期间高度且在特定空间表达,但在第12周及之后则不表达。同样,与年龄匹配的正常胎盘极低水平的表达相比,完全性葡萄胎的细胞滋养层细胞中观察到PAR1和PAR3的高表达水平。总之,我们的数据表明PAR1和PAR3参与了局限性和非局限性的病理性滋养层细胞侵袭。

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