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:PD-L1/PD-1 blockage enhanced the cytotoxicity of natural killer cell on the non-small cell lung cancer (NSCLC) by granzyme B secretion.
PD-L1/PD-1 blockage enhanced the cytotoxicity of natural killer cell on the non-small cell lung cancer (NSCLC) by granzyme B secretion.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
本研究表明,PD-L1/PD-1 阻断通过颗粒酶 B 分泌增强了 NSCLC 中 NK 细胞的细胞毒性。
探讨 PD-L1/PD-1 阻断对非小细胞肺癌(NSCLC)中NK 细胞细胞毒性的作用。
采用非放射性细胞毒性检测试剂盒,评估两种 NSCLC 细胞系 Calu-1 和 H460 对新鲜分离健康供者 NK 细胞细胞溶解作用的敏感性。采用 Western blot、流式细胞术(FACS)、ELISA 和抗体阻断实验确定相关机制,并收集 NSCLC 患者分离的 NK 细胞开展功能实验。
NK 细胞以剂量依赖性方式裂解 Calu-1 和 H460 细胞。在所有效靶比下,H460 对 NK 细胞介导裂解的敏感性均低于 Calu-1。流式细胞术和 Western blot 结果显示,H460 细胞 PD-L1 表达高于 Calu-1。使用抗 PD-L1 抗体阻断 PD-L1/PD-1 相互作用后,NK 细胞对 H460 的特异性裂解增强。NSCLC 患者来源 NK 细胞中也观察到这一结果。
本研究揭示,阻断 PD-L1/PD-1 可通过促进颗粒酶 B 分泌增强 NSCLC 中 NK 细胞的细胞毒性。这项研究将有助于通过检测肿瘤 PD-L1 表达实现更精准的肺癌治疗。
To explore the role of PD-L1/PD-1 blockage in the cytotoxicity of natural killer cell in NSCLC.
Two NSCLC cell lines, Calu-1 and H460, were tested for susceptibility to the cytolytic activity of freshly isolated healthy donor NK cells by a non-radioactive cellular cytotoxicity assay kit. Western blot analysis, FACS, ELISA and antibody blockage experiments were conducted to determine the mechanisms. NK cells isolated from NSCLC patients were also collected for functional assays.
Calu-1 and H460 cells were lysed by NK cells in a dose-dependent manner. H460 cells showed less susceptibility to NK cell-mediated lysis than Calu-1 cells at all ratios. The expression of PD-L1 on H460 cells was higher than that on Calu-1 cells, as determined by FACS and western blot analysis. The specific lysis of H460 cells by NK cells was enhanced when the PD-L1/PD-1 interaction was blocked by anti-PD-L1 antibody. This finding was also demonstrated in NK cells isolated from NSCLC patients.
The present study revealed that PD-L1/PD-1 blockage enhanced the cytotoxicity of natural killer cells in NSCLC via granzyme B secretion. This study will greatly facilitate the precise treatment of lung cancer through determination of PD-L1 expression in tumors.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。