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首页> 外文期刊>Reproduction: The official journal of the Society for the Study of Fertility >Interleukin-8 (CXCL8) stimulates trophoblast cell migration and invasion by increasing levels of matrix metalloproteinase (MMP)2 and MMP9 and integrins α5 and β1
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Interleukin-8 (CXCL8) stimulates trophoblast cell migration and invasion by increasing levels of matrix metalloproteinase (MMP)2 and MMP9 and integrins α5 and β1

机译:白介素8(CXCL8)通过增加基质金属蛋白酶(MMP)2和MMP9以及整联蛋白α5和β1的水平来刺激滋养细胞迁移和侵袭

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Interleukin-8 (IL8/CXCL8) is present in decidua and trophoblast, which also expresses the IL8 receptors, CXCR1 and CXCR2. IL8 was shown to stimulate trophoblast migration. Matrix metalloproteinase (MMP)2, MMP9, and integrins α_(5)β_(1) and α_(1)β_(1) were found to play important roles in trophoblast invasion. We hypothesized that IL8 would increase this cell migration and invasion by HTR-8/SVneo cells through the activity of MMPs and integrins. Isolated first trimester of pregnancy cytotrophoblast (CT) and HTR-8/SVneo cell line were used. Migration was studied by monolayer wounding test, and invasion by Matrigel invasion test. The effects of IL8 on MMPs and integrin subunit expression were determined in HTR-8/SVneo cells by gelatin zymography and western blot respectively. The results that were obtained showed that exogenous IL8 stimulated HTR-8/SVneo cell migration and invasion. MMP2 and MMP9 levels were stimulated to 182% ( P <0.01) and 134% ( P <0.01) respectively. Integrin α_(5) expression was increased to 119% ( P <0.05) and integrin β_(1) expression to 173% ( P <0.001) of the control values. The data that were obtained show for the first time the sensitivity of the HTR-8/SVneo cells, in addition to isolated first trimester CT, to IL8. Exogenous IL8/CXCL8 increased trophoblast cell migration and invasion, which may be partly attributable to stimulation of MMP2 and MMP9 levels and an increase in integrins. HTR-8/SVneo cell viability and proliferation were also increased.
机译:白细胞介素8(IL8 / CXCL8)存在于蜕膜和滋养细胞中,也表达IL8受体CXCR1和CXCR2。已证明IL8刺激滋养细胞迁移。发现基质金属蛋白酶(MMP)2,MMP9和整联蛋白α_(5)β_(1)和α_(1)β_(1)在滋养细胞入侵中起重要作用。我们假设IL8将通过MMP和整合素的活性增加HTR-8 / SVneo细胞的这种细胞迁移和侵袭。使用了分离的妊娠早孕滋养细胞(CT)和HTR-8 / SVneo细胞系。通过单层伤口测试研究迁移,并通过基质胶侵袭测试研究侵袭。分别通过明胶酶谱法和Western印迹法测定HTR-8 / SVneo细胞中IL8对MMPs和整联蛋白亚基表达的影响。获得的结果表明,外源IL8刺激HTR-8 / SVneo细胞迁移和侵袭。 MMP2和MMP9水平分别被刺激到182%(P <0.01)和134%(P <0.01)。整合素α_(5)表达增加至对照值的119%(P <0.05),整合素β_(1)表达增加至对照值的173%(P <0.001)。所获得的数据首次显示了HTR-8 / SVneo细胞,除了分离的孕早期CT以外,还对IL8敏感。外源IL8 / CXCL8增加了滋养层细胞的迁移和侵袭,这可能部分归因于MMP2和MMP9水平的刺激以及整联蛋白的增加。 HTR-8 / SVneo细胞的活力和增殖也增加了。

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