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:Membrane-Anchored pH-Responsive DNA Nanodevice Enhances Natural-Killer-Cell Interaction Specificity toward Tumor Cells.
Membrane-Anchored pH-Responsive DNA Nanodevice Enhances Natural-Killer-Cell Interaction Specificity toward Tumor Cells.
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膜相关蛋白介导的细胞间相互作用对基于细胞的疗法至关重要,然而实现高特异性仍是一项重大挑战。在本研究中,我们开发了一种非遗传性、肿瘤微环境(TME)响应性DNA纳米装置,以增强自然杀伤(NK)细胞对肿瘤细胞的靶向精度。该纳米装置由用于NK细胞膜锚定的两亲性DNA四面体支架和包含pH敏感DNA三链体的CD71特异性适配体组成,用于肿瘤靶向。在正常生理pH下,该纳米装置保持非活性状态,防止脱靶结合。暴露于酸性TME后,三链体结构稳定,使适配体能够采取功能性构象以特异性识别CD71。这种TME响应性肿瘤相关抗原靶向策略显著增强了NK细胞识别和裂解肿瘤细胞的特异性。
Cellular interactions mediated by membrane-associated proteins are crucial for cell-based therapies, yet achieving high specificity remains a significant challenge. In this work, we developed a nongenetic, tumor microenvironment (TME)-responsive DNA nanodevice to enhance the targeting precision of natural killer (NK) cells against tumor cells. This nanodevice comprises an amphiphilic DNA tetrahedral scaffold for NK-cell membrane anchoring and a CD71-specific aptamer incorporating a pH-sensitive DNA triplex for tumor targeting.
Under normal physiological pH, the nanodevice maintains an inactive state, preventing off-target binding. Upon exposure to the acidic TME, the triplex structure stabilizes, enabling the aptamer to adopt a functional conformation for specific CD71 recognition. This TME-responsive tumor-associated antigen targeting strategy significantly enhances the specificity of NK cells in recognizing and lysing tumor cells.
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