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The differential effect of endothelial cell factors on in vitro motility of metastatic and non metastatic cells

机译:内皮细胞因子对转移和非转移细胞体外运动的差异效应

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Motility of tumor cells plays a critical role in tumor metastasis, and as such is a target for intervention. The motility of Calu-1 epithelial lung carcinoma cells is up-regulated when placed in co-culture with human umbilical vein endothelialcells (HUVECs), while that of non-metastatic L132 lung epithelial cells is not. In order to determine the major factor(s) causing these changes in epithelial cell motility, the motile response of both cell types to HUVEC secreted factors - soluble, on the HUVECs themselves, and secreted to the extracellular matrix (ECM) - and to individual ECM proteins was measured by obtaining cell track data with time-lapse videomicroscopy and fitting it to a persistent random walk model of motility. None of the factorstested had a large up-regulatory effect on L132 cell motility, but the Calu-1 cell motility was up-regulated by the HUVEC secreted ECM, and was up-regulated differentially by the individual ECM proteins tested. Flow cytometry analysis showed that theexpression levels of the integrin subunits β1, α2, and α6 are significantly higher on the Calu-1 cells than on the L132 cells, implicating a role for integrins in the observed motile behaviors of these cell lines.
机译:肿瘤细胞的动力在肿瘤转移中发挥着关键作用,因此是干预的目标。当用人脐静脉内皮细胞(HUVECS)置于共培养时,钙肺肺癌细胞的动力是上调的,而非转移性L132肺上皮细胞的含量是上调的。为了确定导致上皮细胞运动中的这些变化的主要因素,细胞类型对Huvec分泌因子 - 可溶性,在Huvecs本身上,并分泌到细胞外基质(ECM)和个体通过用时间流逝跳频获得细胞轨道数据并将其装配到持续随机行走模型的运动能力来测量ECM蛋白。没有任何因子对L132细胞运动具有巨大的调节作用,但是通过Huvec分泌的ECM上调Calu-1细胞活性,并通过测试的个体ECM蛋白质差异上调。流式细胞术分析表明,整合蛋白亚基β1,α2和α6的表达水平在Calu-1细胞上显着高于L132细胞,这暗示了这些细胞系的观察到的运动行为中的整合蛋白的作用。

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