重编程
表型
巨噬细胞极化
材料科学
活性氧
肿瘤微环境
癌症研究
纳米颗粒
IRF5公司
免疫
细胞生物学
肿瘤进展
肿瘤细胞
纳米技术
免疫系统
先天免疫系统
生物
细胞
免疫学
生物化学
癌症
遗传学
干扰素调节因子
基因
作者
Yanhui Zheng,Yaobao Han,Tingting Wang,Hanghang Liu,Qiao Sun,Shijun Hu,Jianquan Chen,Zhen Li
标识
DOI:10.1002/adfm.202270072
摘要
Reprogramming Tumor-Associated Macrophages In article number 2108971, Zhen Li and co-workers find that ultra-small Cu2−xSe nanoparticles can effectively polarize tumor-associated macrophages (TAMs) from the tumor-supportive M2 phenotype into anti-tumor M1 phenotype to significantly boost anti-tumor immunity through a novel mechanism. The nanoparticles can generate reactive oxygen species to trigger polarization through the novel ROS-TRAF6-IRF5-IL-23 signaling pathway, rather than the classic ROS-NF-?B-iNOS pathway.
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