Nishida Y, Hayashi Y, Imai Y, Itoh H
Department of Pathology, Kobe University School of Medicine.
Kobe J Med Sci. 1998 Feb;44(1):31-43.
In pregnancy the decrease in fibrinolytic activity has been described to date by many researchers. The placenta is a source of both plasminogen activator inhibitor type 2 (PAI-2) and type 1 (PAI-1). The PAI-2 was originally detected in the human placenta, which inhibits urokinase-type plasminogen activator (uPA) while it is unable to inhibit tissue type plasminogen activator (tPA). The urokinase-type plasminogen (uP) is activated by u-PA and urokinase-type plasminogen activator receptor (uPAR). We studied the expression and the localization of u-PAR in the human placenta by in situ hybridization, immunohistochemically and by use of Northern blot analysis. These data show that the decidualized endometorium have the cells with the greatest uPAR mRNA expression in the placenta, and syncytiotrophoblasts express lower level of uPAR mRNA.
迄今为止,许多研究人员都描述了孕期纤溶活性的降低。胎盘是2型纤溶酶原激活物抑制剂(PAI - 2)和1型纤溶酶原激活物抑制剂(PAI - 1)的来源。PAI - 2最初在人胎盘中被检测到,它能抑制尿激酶型纤溶酶原激活物(uPA),但不能抑制组织型纤溶酶原激活物(tPA)。尿激酶型纤溶酶原(uP)由u - PA和尿激酶型纤溶酶原激活物受体(uPAR)激活。我们通过原位杂交、免疫组织化学以及Northern印迹分析研究了uPAR在人胎盘中的表达和定位。这些数据表明,在胎盘中,蜕膜化的子宫内膜细胞具有最高的uPAR mRNA表达,而合体滋养层细胞表达的uPAR mRNA水平较低。