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Molecular mechanism of the effect of angiopoietin-like protein 8 on the proliferation invasion and migration of placental trophoblasts in preeclampsia

机译:子痫前期血管生成素样蛋白8对胎盘滋养细胞增殖侵袭和迁移影响的分子机制

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摘要

Preeclampsia (PE) is a pregnancy-specific systemic disorder characterized by various manifestations of organ dysfunction. Inadequate trophoblastic invasion of the uterine wall is involved in the pathogenesis of PE. Angiopoietin-like protein 8 (ANGPTL8) serves an important role in cardiovascular disease development and may have a potential effect on cell proliferation. In the present study, downregulation of ANGPTL8 promoted cell proliferation, decreased p21 expression, and increased the expression levels of cyclin-dependent kinase 2 and proliferating cell nuclear antigen in HTR8/SVneo cells. Silencing of ANGPTL8 led to significant acceleration in cell migration and invasion, and markedly enhanced the matrix metalloproteinase (MMP)-2 and MMP-9 expression levels. In addition, the protein expression levels of tissue inhibitor of matrix metalloproteinase (TIMP)-1 and TIMP-2 were decreased in the group transfected with small interfering RNA (si)-ANGPTL8-1 as compared with those in the control and si-negative control groups. Taken together, these results indicated that ANGPTL8 downregulation promoted the proliferation, migration and invasion of trophoblast cells. Thus, ANGPTL8 suppresses the viability, proliferation, migration and invasion of trophoblast cells, and may be a potential therapeutic target for the clinical treatment of PE.
机译:子痫前期(PE)是一种妊娠特定的全身性疾病,其特征是器官功能障碍的各种表现。子宫壁滋养细胞浸润不足与PE的发病机制有关。血管生成素样蛋白8(ANGPTL8)在心血管疾病的发展中起重要作用,并可能对细胞增殖产生潜在影响。在本研究中,ANGPTL8的下调促进了HTR8 / SVneo细胞的细胞增殖,降低了p21表达,并提高了细胞周期蛋白依赖性激酶2和增殖细胞核抗原的表达水平。 ANGPTL8的沉默导致细胞迁移和侵袭的显着加速,并显着增强了基质金属蛋白酶(MMP)-2和MMP-9的表达水平。此外,转染小干扰RNA(si)-ANGPTL8-1的组与对照组和si阴性组相比,基质金属蛋白酶(TIMP)-1和TIMP-2的组织抑制剂蛋白表达水平降低。对照组。综上所述,这些结果表明ANGPTL8的下调促进了滋养细胞的增殖,迁移和侵袭。因此,ANGPTL8抑制滋养细胞的活力,增殖,迁移和侵袭,并且可能是PE临床治疗的潜在治疗靶标。

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