Nishizawa Haruki, Pryor-Koishi Kanako, Suzuki Machiko, Kato Takema, Kogo Hiroshi, Sekiya Takao, Kurahashi Hiroki, Udagawa Yasuhiro
Department of Obstetrics and Gynecology, Fujita Health University School of Medicine, 1-98 Dengakugakubo, Kutsukake, Toyoake, Aichi 470-1192, Japan.
Mol Hum Reprod. 2008 Oct;14(10):595-602. doi: 10.1093/molehr/gan054. Epub 2008 Sep 18.
Pregnancy-associated plasma protein-A and -A2 (PAPP-A and -A2) are proteases that cleave insulin-like growth factor-binding proteins (IGFBPs), resulting in local activation of IGF signaling pathways. Here, we examined PAPP-A and -A2 mRNA and protein levels in placenta and maternal sera from women with pre-eclampsia and compared them with samples from uncomplicated pregnancy. PAPP-A2 but not PAPP-A mRNA and protein were elevated in pre-eclamptic placenta (P < 0.01). PAPP-A2 is normally produced in placental syncytiotrophoblast cells and maternal decidua. PAPP-A2 in syncytiotrophoblast cells was dramatically increased in pre-eclampsia. Maternal serum concentrations of PAPP-A2 but not PAPP-A were also significantly elevated in pre-eclampsia as compared with uncomplicated pregnancy. mRNA levels of IGFBP5, a specific substrate for PAPP-A2 protease activity, were also significantly increased, suggesting a potential role for IGFBP5 in fetal and placental growth suppression during pre-eclampsia. However, IGFBP5 protein levels were not increased in placenta from pre-eclampsia, possibly due to cleavage by up-regulated PAPP-A2. These data might imply that PAPP-A2 may be up-regulated in pre-eclamptic pregnancy to compensate for IGFBP5-mediated suppression of the IGF pathway, although final birthweights are still low in pre-eclamptic pregnancy.
妊娠相关血浆蛋白-A和-A2(PAPP-A和-A2)是裂解胰岛素样生长因子结合蛋白(IGFBPs)的蛋白酶,可导致IGF信号通路的局部激活。在此,我们检测了子痫前期妇女胎盘和母血清中PAPP-A和-A2的mRNA及蛋白水平,并将其与正常妊娠样本进行比较。子痫前期胎盘组织中PAPP-A2的mRNA和蛋白水平升高,而PAPP-A未升高(P<0.01)。PAPP-A2通常由胎盘合体滋养层细胞和母体蜕膜产生。子痫前期时,合体滋养层细胞中的PAPP-A2显著增加。与正常妊娠相比,子痫前期孕妇血清中PAPP-A2浓度也显著升高,而PAPP-A未升高。PAPP-A2蛋白酶活性的特异性底物IGFBP5的mRNA水平也显著升高,提示IGFBP5在子痫前期胎儿和胎盘生长受限中可能发挥作用。然而,子痫前期胎盘组织中IGFBP5蛋白水平未升高,可能是由于上调的PAPP-A2对其进行了裂解。这些数据可能意味着,子痫前期妊娠中PAPP-A2可能上调,以补偿IGFBP5介导的IGF通路抑制,尽管子痫前期妊娠的最终出生体重仍然较低。