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Lipid tethering of breast tumor cells enables real-time imaging of free-floating cell dynamics and drug response

机译:乳腺肿瘤细胞的脂质束缚可实现自由漂浮细胞动力学和药物反应的实时成像

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摘要

Free-floating tumor cells located in the blood of cancer patients, known as circulating tumor cells (CTCs), have become key targets for studying metastasis. However, effective strategies to study the free-floating behavior of tumor cells in vitro have been a major barrier limiting the understanding of the functional properties of CTCs. Upon extracellular-matrix (ECM) detachment, breast tumor cells form tubulin-based protrusions known as microtentacles (McTNs) that play a role in the aggregation and re-attachment of tumor cells to increase their metastatic efficiency. In this study, we have designed a strategy to spatially immobilize ECM-detached tumor cells while maintaining their free-floating character. We use polyelectrolyte multilayers deposited on microfluidic substrates to prevent tumor cell adhesion and the addition of lipid moieties to tether tumor cells to these surfaces through interactions with the cell membranes. This coating remains optically clear, allowing capture of high-resolution images and videos of McTNs on viable free-floating cells. In addition, we show that tethering allows for the real-time analysis of McTN dynamics on individual tumor cells and in response to tubulin-targeting drugs. The ability to image detached tumor cells can vastly enhance our understanding of CTCs under conditions that better recapitulate the microenvironments they encounter during metastasis.
机译:位于癌症患者血液中的自由漂浮肿瘤细胞(称为循环肿瘤细胞(CTC))已成为研究转移的关键靶标。但是,研究肿瘤细胞在体外的自由漂浮行为的有效策略已经成为限制对CTC功能特性的理解的主要障碍。在细胞外基质(ECM)脱离后,乳腺肿瘤细胞会形成基于微管蛋白的突出物,称为微触角(McTNs),在肿瘤细胞的聚集和重新附着中发挥作用,以提高其转移效率。在这项研究中,我们设计了一种策略,可以在空间上固定ECM分离的肿瘤细胞,同时保持其自由漂浮的特性。我们使用沉积在微流体基质上的聚电解质多层膜,以防止肿瘤细胞粘附以及通过与细胞膜的相互作用将脂质部分添加到系留肿瘤细胞的这些表面上。该涂层保持光学透明,从而可以在可行的自由漂浮细胞上捕获McTN的高分辨率图像和视频。此外,我们显示,系留系统可对单个肿瘤细胞上的McTN动态进行实时分析,并响应微管蛋白靶向药物。在更好地概括它们在转移过程中遇到的微环境的条件下,对分离的肿瘤细胞进行成像的能力可以极大地增强我们对四氯化碳的了解。

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