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:Development of a novel GAK solution for efficient hypothermic preservation of NK cell viability and anti-tumor function.
Development of a novel GAK solution for efficient hypothermic preservation of NK cell viability and anti-tumor function.
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本研究揭示了 NK 细胞在低温条件下的多种死亡机制,并成功开发了一种成分明确且高效的 GAK 溶液。GAK 溶液为 NK 细胞的低温保存提供了新方法,有助于 NK 细胞产品高效便捷地运输,对加速细胞免疫治疗的临床转化具有重要的现实意义。
NK 细胞在当前的免疫治疗模式中展现出显著潜力。低温保存是NK细胞产品临床运输和临时储存的关键步骤。然而,在此过程中,细胞活力和功能均显著下降。核心损伤机制尚不明确,且目前缺乏有效、专用的保存方案。本研究旨在阐明低温保存期间细胞死亡的主要方式并维持NK细胞效力。
本研究首先评估了不同静脉输液和温度对NK细胞保存效率的影响。随后,利用多种细胞死亡抑制剂、分子生物标志物检测和电子显微镜技术,系统阐明了细胞死亡方式。基于这些发现,我们优化了表现最佳的液体,用葡萄糖替代乳酸钠以增强能量供应,添加抗氧化剂α-生育酚以减轻氧化应激,并将钾离子浓度提高至22.5 mM以抑制过度营养摄取及相关氧化损伤。这些优化被纳入一种新配方,命名为GAK溶液。通过体外细胞活力和细胞毒性试验以及体内白血病异种移植模型,全面评估了保存效果。
4 °C 保存远优于 25 °C。在测试的静脉输液中,乳酸林格液在维持 NK 细胞活力和功能方面表现出最高效力。NK 细胞在低温保存过程中经历复杂的死亡通路,具体为铁死亡、焦亡和坏死性凋亡。我们优化的 GAK 有效缓解能量耗竭和氧化应激,在低温保存后显著维持 NK 细胞的活力以及对多种肿瘤细胞的有效细胞毒性能力。体内实验进一步表明,保存在 GAK 溶液中的 NK 细胞维持了显著的抗肿瘤活性,这有助于延长荷瘤小鼠的生存期。
Natural killer cells exhibit significant potential within current immunotherapeutic modalities. Hypothermic preservation is a critical step for the clinical transportation and temporary storage of NK cell products. However, during this process, both cell viability and function significantly decrease. The core damage mechanisms remain unclear, and effective, specialized preservation protocols are currently lacking. This study aimed to elucidate the primary modes of cell death and maintain NK cell potency during hypothermic preservation.
This study first evaluated the effects of different intravenous fluids and temperatures on NK cell preservation efficiency. Subsequently, various cell death inhibitors, molecular biomarker assays, and electron microscopy techniques were utilized to systematically elucidate the modes of cell death. Based on these findings, we optimized the best-performing fluids by replacing sodium lactate with glucose to enhance energy supply, adding the antioxidant α-tocopherol to mitigate oxidative stress, and elevating the potassium ion concentration (to 22.5 mM) to suppress excessive nutrient uptake and associated oxidative damage. These optimizations were incorporated into a new formulation designated as the GAK solution. The preservation efficacy was comprehensively assessed through in vitro cell viability and cytotoxicity assays, as well as an in vivo leukemia xenograft model.
Storage at 4 °C was much better than at 25 °C. Among the tested intravenous fluids, lactated Ringer's demonstrated the highest efficacy in preserving NK cell viability and function. NK cells undergo complex death pathways during hypothermic preservation, specifically ferroptosis, pyroptosis, and necroptosis. Our optimized GAK effectively mitigates energy depletion and oxidative stress, significantly maintaining the viability and potent cytotoxic capacity of NK cells against various tumor cells after hypothermic storage. In vivo experiments further demonstrated that NK cells preserved in the GAK solution maintained significant antitumor activity, which contributed to prolonged survival in tumor-bearing mice.
This study revealed multiple death mechanisms of NK cells during hypothermia and successfully developed a well-defined and highly efficient GAK solution. The GAK solution presents a new approach to the hypothermic preservation of NK cells, facilitating the efficient and convenient transport of NK cell products, which has significant practical implications for the accelerated clinical adoption of cellular immunotherapy.
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