Clark Nicholas M, Bos Paula D
Department of Pathology, Integrative Life Sciences Graduate Program, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Department of Pathology, Massey Cancer Center, Virginia Commonwealth University School of Medicine, Richmond, VA, USA.
Methods Mol Biol. 2019;1884:151-160. doi: 10.1007/978-1-4939-8885-3_10.
Characterization of individual cell populations from the tumor microenvironment is critical to understand their functional contribution to tumor progression. Magnetic bead enrichment and fluorescence-activated cell sorting (FACS) allow for the isolation of specific cell types that can be used in downstream applications, including in vitro and in vivo functional studies and molecular profiling. In this chapter, we describe the process of isolation of tumor-associated macrophages (TAMs) from primary murine breast tumors subsequent to therapeutic or experimental intervention. Additionally, we further detail how to analyze their ability to support tumor cell growth by co-injecting isolated TAMs with tumor cells orthotopically into the mammary gland of immune-deficient hosts, and monitoring tumor progression by live imaging and caliper measurement.
表征肿瘤微环境中的单个细胞群体对于理解它们对肿瘤进展的功能贡献至关重要。磁珠富集和荧光激活细胞分选(FACS)可用于分离特定细胞类型,这些细胞类型可用于下游应用,包括体外和体内功能研究以及分子谱分析。在本章中,我们描述了在治疗或实验干预后从原发性小鼠乳腺肿瘤中分离肿瘤相关巨噬细胞(TAM)的过程。此外,我们进一步详细介绍了如何通过将分离的TAM与肿瘤细胞原位共注射到免疫缺陷宿主的乳腺中,并通过实时成像和卡尺测量监测肿瘤进展,来分析它们支持肿瘤细胞生长的能力。