巨噬细胞
巨噬细胞极化
表型
癌细胞
免疫系统
细胞生物学
炎症
分泌物
胶体金
化学
M2巨噬细胞
纳米颗粒
生物物理学
材料科学
体外
纳米技术
生物
癌症
免疫学
生物化学
基因
遗传学
作者
Shouning Yang,Yanmin Zhang,Sijia Lü,Lin Yang,Shaoning Yu,Huayan Yang
出处
期刊:ACS applied bio materials
[American Chemical Society]
日期:2021-03-11
卷期号:4 (4): 3214-3223
被引量:11
标识
DOI:10.1021/acsabm.0c01608
摘要
Macrophage cells are plastic and can be polarized into opposing phenotypes, pro-inflammatory (M1-like cells) or anti-inflammatory (M2-like cells). Reprograming of M2-like cells into M1 phenotype will contribute significantly to combatting cancer. Gold nanoparticles (AuNPs) are intensively studied in various fields for their distinctive photo-chemical properties. However, the immune response of AuNPs is still unclear. In this study, AuNPs and CaCO3-encapsulated Au nanoparticles (Au@CaCO3 NPs) were synthesized as stimuli for macrophage modulation. Co-incubation of AuNPs and macrophages leads to a dramatically elongated macrophage cell morphology. Moreover, increased expression of M2 biomarker and M2-inducing cytokines suggests that AuNPs induce macrophage polarization toward M2 phenotype. More interestingly, the co-incubation of Au@CaCO3 NPs and macrophage cells resulted in a round cellular morphology and induced the secretion of M1 biomarker and inflammatory cytokines. Our studies demonstrate that the strategy of CaCO3-encapsulated Au nanoparticles can be used in modulating the polarization of M1 macrophages. Our strategy provides an efficient method for activating inflammation in macrophages, which will be useful for the application of nanoparticles in cancer therapy.
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