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:Cationic Magnetic Nanoparticles Activate Natural Killer Cells for the Treatment of Glioblastoma.
Cationic Magnetic Nanoparticles Activate Natural Killer Cells for the Treatment of Glioblastoma.
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血脑屏障(BBB)和胶质母细胞瘤(GBM)的免疫抑制性微环境会严重阻碍自然杀伤(NK)细胞浸润及其活性,从而降低其治疗GBM的临床疗效。为应对这一挑战,研究者构建了一种工程化活体材料HEFDS-NK细胞,旨在增强NK细胞穿越BBB的能力并提高其对GBM的细胞毒作用。HEFDS由经阳离子聚乙烯亚胺(PEI)、硒代半胱氨酸(Sec)和透明质酸钠(HA)修饰的磁性纳米颗粒组成;将其与NK细胞共培养,制备HEFDS-NK细胞。在HA和磁靶向协助下,HEFDS-NK细胞可有效穿越BBB并定位于GBM部位。
此外,PEI可提高NK细胞上C-X-C趋化因子受体4型(CXCR4)和C-C趋化因子受体4型(CCR4)的表达,增强其对GBM的识别能力和细胞毒作用。Sec还可增强NK细胞针对GBM的免疫活性。HEFDS-NK细胞识别GBM后会被激活并产生颗粒酶B、穿孔素和IFN-γ,最终有效治疗GBM。
本研究展示了一种有效治疗GBM的方法,可同时增强NK细胞活性及其穿越BBB的能力,为GBM治疗提供了创新且高精度的策略。
The blood-brain barrier (BBB) and the immunosuppressive microenvironment of glioblastoma (GBM) severely hinder the infiltration and activity of natural killer (NK) cells, thereby reducing their clinical efficacy in GBM treatment. To address this challenge, we introduced an engineered living material, HEFDS-NK cells, designed to enhance the penetration of NK cells across the BBB and improve their cytotoxicity against GBM.
HEFDS comprises magnetic nanoparticles modified using cationic polyethylenimine (PEI), selenocysteine (Sec), and sodium hyaluronate (HA) and cocultured with NK cells to form HEFDS-NK cells. With the assistance of HA and magnet targeting, HEFDS-NK cells can effectively cross the BBB and localize at the GBM site.
Moreover, PEI enhances the expression of C-X-C chemokine receptor type 4 (CXCR4) and C-C chemokine receptor type 4 (CCR4) on NK cells, thereby improving their recognition and cytotoxicity against GBM.
Additionally, Sec boosts the immune activity of NK cells against GBM. Upon recognizing GBM, the activated HEFDS-NK cells produce Granzyme B, Perforin, and IFN- , ultimately achieving effective therapy for GBM.
This study demonstrates an effective treatment of GBM while enhancing NK cell activity and their ability to penetrate the BBB, providing an innovative and high-precision therapeutic approach for GBM.
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