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Cancer Cells Induced to Express Mesenchymal Phenotype Release Exosome-like Extracellular Vesicles Carrying Tissue Factor

机译:癌细胞诱导表达间质表型释放外来样样细胞外囊泡携带组织因子。

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摘要

Aggressive epithelial cancer cells frequently adopt mesenchymal characteristics and exhibit aberrant interactions with their surroundings, including the vasculature. Whether the release/uptake of extracellular vesicles (EVs) plays a role during these processes has not been studied. EVs are heterogeneous membrane structures that originate either at the surface (microparticles), or within (exosomes) activated or transformed cells, and are involved in intercellular trafficking of bioactive molecules. Here, we show that epithelial cancer cells (A431, DLD-1) adopt mesenchymal features (epithelial-to-mesenchymal transition-like state) upon activation of epidermal growth factor receptor (EGFR) coupled with blockade of E-cadherin. This treatment leads to a coordinated loss of EGFR and tissue factor (TF) from the plasma membrane and coincides with a surge in emission of small, exosome-like EVs containing both receptors. TF (but not EGFR) is selectively up-regulated in EVs produced by mesenchymal-like cancer cells and can be transferred to cultured endothelial cells rendering them highly procoagulant. We postulate that epithelial-to-mesenchymal transition-like changes may alter cancer cell interactions with the vascular systems through altered vesiculation and TF shedding.
机译:侵袭性上皮癌细胞经常具有间充质特征,并与周围环境(包括脉管系统)表现出异常的相互作用。尚未研究在这些过程中是否释放/摄取细胞外囊泡(EVs)。电动汽车是异质膜结构,起源于表面(微粒)或在(外泌体)活化或转化的细胞内,并参与生物活性分子的细胞间运输。在这里,我们显示上皮癌细胞(A431,DLD-1)在激活表皮生长因子受体(EGFR)并阻断E-钙黏着蛋白后采用间充质特征(上皮向间充质样转变状态)。这种治疗导致质膜中EGFR和组织因子(TF)的协调丧失,并且与含有两种受体的小型,外体样EV的发射激增相吻合。 TF(但不是EGFR)在间充质样癌细胞产生的EV中选择性上调,并且可以转移到培养的内皮细胞中,使其高度促凝。我们假设上皮到间充质样转变可能通过改变囊泡和TF脱落而改变癌细胞与血管系统的相互作用。

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