Davis Beckley K
Department of Biology, Franklin & Marshall College, Lancaster, PA, USA.
Methods Mol Biol. 2019;1960:41-55. doi: 10.1007/978-1-4939-9167-9_3.
Macrophages are cellular components of the immune system that are essential for responding to pathogens, initiating inflammation and maintaining tissue homeostasis. Isolation, culture, and functional characterization of bone marrow-derived macrophages from mice are exceptionally powerful in vitro techniques used to examine aspects of macrophage biology, including effector functions, such as phagocytosis, cytokine secretion, oxidative burst, migration, and antigen processing and presentation. These studies can be carried out using wild-type, gene-ablated, and/or transgenic mice. The quantity, purity, and ease of culture of these cells enhance their utility for primary cell cultures to understand macrophage biology. Mouse macrophages have become a cognate animal model for the study of human macrophage biology and disease. This chapter outlines protocols used to generate, polarize, quantitate, and functionally evaluate macrophages derived from bone marrow precursor cells.
巨噬细胞是免疫系统的细胞组成部分,对于应对病原体、引发炎症和维持组织稳态至关重要。从小鼠中分离、培养和功能鉴定骨髓来源的巨噬细胞,是用于研究巨噬细胞生物学各个方面的极为强大的体外技术,包括吞噬作用、细胞因子分泌、氧化爆发、迁移以及抗原加工和呈递等效应功能。这些研究可以使用野生型、基因敲除和/或转基因小鼠来进行。这些细胞的数量、纯度和培养的简便性提高了它们在原代细胞培养中用于理解巨噬细胞生物学的效用。小鼠巨噬细胞已成为研究人类巨噬细胞生物学和疾病的同源动物模型。本章概述了用于生成、极化、定量和功能评估源自骨髓前体细胞的巨噬细胞的方案。