外渗
肿瘤微环境
纳米颗粒
细胞外基质
巨噬细胞
基质
肿瘤细胞
纳米技术
癌症研究
化学
生物物理学
材料科学
病理
医学
生物
体外
生物化学
免疫组织化学
作者
Zachary P. Lin,Luan N. Nguyen,Ben Ouyang,Presley MacMillan,Jessica Ngai,Benjamin R. Kingston,Stefan M. Mladjenovic,Warren C. W. Chan
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-04-12
卷期号:16 (4): 6080-6092
被引量:45
标识
DOI:10.1021/acsnano.1c11578
摘要
Nanoparticles need to navigate a complex microenvironment to target cells in solid tumors after extravasation. Diffusion is currently the accepted primary mechanism for nanoparticle distribution in tumors. However, the extracellular matrix can limit nanoparticle diffusion. Here, we identified tumor-associated macrophages as another key player in transporting and redistributing nanoparticles in the tumor microenvironment. We found tumor-associated macrophages actively migrate toward nanoparticles extravasated from the vessels, engulfing and redistributing them in the tumor stroma. The macrophages can carry the nanoparticles 2–5 times deeper in the tumor than passive diffusion. The amount of nanoparticles transported by the tumor-associated macrophages is size-dependent. Understanding the nanoparticle behavior after extravasation will provide strategies to engineer them to navigate the microenvironment for improved intratumoral targeting and therapeutic effectiveness.
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