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结合 NK 细胞的 TRAIL 偶联脂质体诱导结直肠癌细胞凋亡

英文原题:TRAIL-conjugated liposomes that bind natural killer cells to induce colorectal cancer cell apoptosis.

查看英文原题

TRAIL-conjugated liposomes that bind natural killer cells to induce colorectal cancer cell apoptosis.

PubMed 2023/09/29(内容时间) J Biomed Mater Res A Q2 · IF 3.8(JCR 2025)

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中文摘要

自然杀伤(NK)细胞功能良好是癌症患者预后良好的重要指标,因此NK细胞是预防肿瘤向淋巴结播散的潜在治疗靶点。研究人员构建了经抗CD335抗体修饰、用于靶向NK细胞的脂质体,并负载凋亡配体TRAIL以杀伤癌细胞。脂质体采用薄膜水化法制备后挤出至约100 nm,并通过巯基-马来酰亚胺点击化学偶联蛋白。TRAIL/抗CD335脂质体可成功结合分离的NK细胞。这些被脂质体“搭载”于表面的“超级NK 细胞”,与单独NK细胞相比,可通过TRAIL介导的凋亡更有效地杀伤奥沙利铂耐药SW620细胞和转移性结直肠癌COLO205细胞。在淋巴系统生理性液体剪切应力条件下,超级NK细胞的杀伤效果仍更强。静脉给药后的脂质体分布显示,其至少4天持续存在于脾脏及肿瘤引流肠系膜淋巴结。这些结果表明,脂质体TRAIL装甲化NK细胞可增强其对具有临床相关性的结直肠癌细胞的促凋亡作用,为在结直肠癌转移小鼠模型中开展体内治疗研究奠定了基础。

展开英文摘要原文

Natural killer (NK) cell functionality is a strong indicator of favorable prognosis in cancer patients, making NK cells an appealing therapeutic target to prevent lymph node dissemination.

We engineered liposomes that are conjugated with anti-CD335 antibodies for NK cell targeting, and the apoptotic ligand TRAIL to kill cancer cells. Liposomes were made using a thin film hydration method followed by extrusion to approximately 100 nm in diameter and conjugation of proteins via thiol-maleimide click chemistry.

TRAIL/anti-CD335 liposomes successfully bound to isolated NK cells. Once piggybacked to the surface of NK cells, these "Super Natural Killer Cells" were able to more effectively kill oxaliplatin-resistant SW620 cells and metastatic COLO205 colorectal cancer cells via TRAIL-mediated apoptosis compared to NK cells alone.

Importantly, Super NK cells were more effective under physiological levels of fluid shear stress found in the lymphatics. Liposome biodistribution after intravenous administration confirmed the sustained presence of liposomes within the spleen and tumor draining mesenteric lymph nodes for at least 4 days.

These results demonstrate the enhanced apoptotic effects of NK cells armored with liposomal TRAIL against clinically relevant colorectal cancer cells, providing the groundwork for in vivo treatment studies in mouse models of colorectal cancer metastasis.

论文信息

作者
Greenlee JD、Zhang Z、Subramanian T、Liu K、King MR
单位
Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.United States
文献类型
美国政府(非公共卫生署)资助研究 · 美国 NIH 资助研究
期刊
Journal of biomedical materials research. Part A2024 Jan
原文标识
PubMed 37772330 · DOI 10.1002/jbm.a.37621