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Modulating Cell-Cell Communication with a High-Throughput Label-Free Cell Assay

机译:高通量无标记细胞测定法调节细胞间通信

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A high-throughput label-free cell assay for modulating cell-cell communication is demonstrated with the Epic system, a resonant waveguide grating sensor platform. Natural killer (NK) cells are known to be able to recognize abnormal cells (e.g., cancer cells and cells presenting intercellular adhesion molecule I [ICAMI] through cell surface receptors) and kill them. In this study, the effect of effecter cells NK92MI on two kinds of target cells, cervical cancer cells (HeLa) and Chinese hamster ovarian cells overexpressing ICAMI (CHO-ICAMI), was examined. Living target cells' response to NK92MI cells was monitored in real time and measured as wavelength shift in picometers. The authors showed that the detectability of target cell response is affected by multiple factors: the ratio of effecter cells to target cells (E/T), the interaction time of the two types of cells, and the target cell type. For example, with the effecter cells NK92MI and the same incubation time of 16 h, a minimal E/T ratio of I is required to detect HeLa cell response, whereas an E/T of 0.5 is sufficient to detect CHO-ICAM I cell response. The authors confirmed that NK92MI cell-mediated target cell cytotoxicity results in negative optical signals and is associated with apoptosis mainly through caspase pathways. Distinct optical signals could be generated with the pretreatment of the target cells with various known pharmaceutical reagents, making the assay useful for discovering new chemicals that may affect cell-cell communications.
机译:利用共振波导光栅传感器平台Epic系统演示了用于调制细胞间通信的高通量无标记细胞测定。已知自然杀伤(NK)细胞能够识别异常细胞(例如癌细胞和通过细胞表面受体呈递细胞间粘附分子I [ICAMI]的细胞)并杀死它们。在这项研究中,研究了效应细胞NK92MI对两种靶细胞的影响,即宫颈癌细胞(HeLa)和过度表达ICAMI的中国仓鼠卵巢细胞(CHO-ICAMI)。实时监测活靶细胞对NK92MI细胞的反应,并以皮米为单位的波长偏移进行测量。作者表明,靶细胞应答的可检测性受多种因素影响:效应细胞与靶细胞的比率(E / T),两种类型细胞的相互作用时间以及靶细胞类型。例如,在效应细胞NK92MI和相同的16小时孵育时间下,检测HeLa细胞反应需要最小的E / T比I,而0.5的E / T足以检测CHO-ICAM I细胞反应。作者证实,NK92MI细胞介导的靶细胞细胞毒性导致负性光信号,并且主要通过caspase途径与细胞凋亡相关。通过使用各种已知的药物试剂对靶细胞进行预处理,可以生成不同的光信号,从而使该测定法可用于发现可能影响细胞-细胞通讯的新化学物质。

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