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:Lung Cancer Organoid System to Evaluate the Cytotoxicity of Natural Killer Cells.
Lung Cancer Organoid System to Evaluate the Cytotoxicity of Natural Killer Cells.
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自然杀伤(NK)细胞因其免疫治疗潜力而日益受到关注,需要快速且准确的平台研究其生物学特性和治疗应用。本研究建立基于肺癌类器官的系统以评估NK细胞的细胞毒性。研究者在基质胶上培养肺癌类器官并与NK细胞共培养;NK细胞可迁移至类器官附近并进入其中。流式细胞分析显示,共培养显著增加类器官细胞死亡,表明该模型适用于评估NK细胞杀伤能力。用TGF抑制剂A83-01预处理NK细胞后,其诱导类器官细胞死亡的能力进一步增强。该类器官共培养体系可重现细胞系实验中的体外细胞毒性评估结果,是研究NK细胞生物学及筛选NK细胞免疫疗法的可靠平台。
Natural killer (NK) cells are gaining growing attention due to their promise for immunotherapy. A fast and accurate system is needed to test NK cell biology and their therapeutic application.
Here, we report a lung cancer organoid-based system to evaluate NK cells' cytotoxicity.
We first established the lung cancer organoids on top of Matrigel, which allows the co-culture with NK cells. When co-cultured, NK cells moved close to and inside the lung cancer organoids. When we analyzed by flow cytometry, co-culture of NK cells induced a significantly higher ratio of cell death of lung cancer organoids, suggesting that lung cancer organoids can be employed to test the cytotoxicity of NK cells.
Finally, the pre-treatment of NK cells with A83-01, a TGF inhibitor, significantly enhanced the cell death of lung cancer organoids by NK cells, indicating that lung cancer organoid-based system faithfully recapitulates cell line-based system in evaluating the in vitro cytotoxicity of NK cells. These data represent that cancer organoid-based NK cell co-culture system is a reliable platform for studying NK cell biology and evaluating their cytotoxicity for screening for NK cell immunotherapy.
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