Macrophage Differentiation and Polarization into an M2-Like Phenotype using a Human Monocyte-Like THP-1 Leukemia Cell Line

THP1细胞系 单核细胞 细胞生物学 肿瘤微环境 细胞培养 细胞因子 巨噬细胞极化 表型 巨噬细胞 生物 电池类型 癌症研究 癌细胞 细胞分化 细胞 免疫系统 免疫学 体外 癌症 遗传学 基因
作者
Katharina M. Scheurlen,Dylan L. Snook,Sarah A. Gardner,M. Robert Eichenberger,Susan Galandiuk
出处
期刊:Journal of Visualized Experiments [MyJOVE]
卷期号: (174) 被引量:17
标识
DOI:10.3791/62652
摘要

Tumor-associated macrophages (TAM) can switch their expression and cytokine profile according to external stimuli. This remarkable plasticity enables TAM to adapt to ongoing changes within the tumor microenvironment. Macrophages can have either primarily pro-inflammatory (M1-like) or anti-inflammatory (M2-like) attributes and can continually switch between these two main states. M2-like macrophages within the tumor environment are associated with cancer progression and poor prognosis in several types of cancer. Many different methods for inducing differentiation and polarization of THP-1 cells are used to investigate cellular and intercellular mechanisms and the effects of TAM within the microenvironment of tumors. Currently, there is no established model for M2-like macrophage polarization using the THP-1 cell line, and the results of expression and cytokine profiles of macrophages due to certain in vitro stimuli vary between studies. This protocol serves as detailed guidance to differentiate THP-1 monocyte-like cells into M0 macrophages and to further polarize cells into an M2-like phenotype within 14 days. We demonstrate the morphological changes of THP-1 monocyte-like cells, differentiated macrophages, and polarized M2-like macrophages using light microscopy. This model is the basis for cell line models investigating the anti-inflammatory effects of TAM and their interactions with other cell populations of the tumor microenvironment.
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