RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Metasurface plasmon resonance platform for high-throughput, label-free, real-time, long-term monitoring of in vitro cancer therapy assessment.
Metasurface plasmon resonance platform for high-throughput, label-free, real-time, long-term monitoring of in vitro cancer therapy assessment.
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提高体外细胞行为的实时和长期评估能力对于基础科学研究和药物开发至关重要。本研究建立了一个基于超表面等离激元共振(MetaSPR)光谱的高通量、实时、无标记、长期细胞分析和药物筛选平台。该平台被应用于监测细胞增殖、药物-靶细胞相互作用、细胞黏附以及NK 细胞介导的细胞裂解。该平台的准确性通过MetaSPR结果与细胞计数试剂盒8(CCK-8)检测/成像信号之间的线性关系得到验证,为进一步实验提供了坚实基础。该平台持续监测细胞增殖、药物-靶细胞相互作用和细胞黏附/铺展,所得结果与使用传统CCK-8和流式细胞术方法获得的结果相当。
此外,通过将NK 细胞与靶细胞以不同效靶比共培养并监测其相互作用,评估了NK 细胞的细胞溶解活性。结果表明,光谱MetaSPR检测系统能够定量评估免疫细胞介导的细胞溶解活性。该平台的快速响应、成本效益、实时监测能力和非侵入性特征可以增强对复杂细胞过程的理解,并为药物筛选和临床诊断创造新的可能性。
Improving real-time and long-term assessment of cellular behaviors in vitro is crucial for basic scientific research and drug development.
This study establishes a high-throughput, real-time, label-free, long-term cell analysis and drug screening platform based on metasurface plasmon resonance (MetaSPR) spectroscopy. This platform was applied to monitor cell proliferation, drug-target cell interactions, cell adhesion, and natural killer cell-mediated cell lysis.
The accuracy of the platform was validated by a linear relationship between the MetaSPR results and cell counting kit 8 (CCK-8) assay/imaging signals, providing a solid foundation for further experiments. This platform consistently monitors cell proliferation, drug-target cell interactions, and cell adhesion/spreading, yielding results comparable to those obtained using traditional CCK-8 and flow cytometry methods.
Additionally, the cytolytic activity of natural killer cells was evaluated by co-culturing them with target cells at varying effector:target ratios and monitoring their interactions. The results demonstrate that the spectroscopic MetaSPR detection system can quantitatively assess cytolytic activity mediated by immune cells.
The rapid response, cost-effectiveness, real-time monitoring capability, and non-invasive characteristics of this platform can enhance the understanding of complex cellular processes and create new possibilities for drug screening and clinical diagnostics.
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