Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ontario, Canada.
Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ontario, Canada; University of Ottawa Centre for Infection, Immunity and Inflammation, Ottawa, K1H 8M5 Ontario, Canada.
J Immunol Methods. 2020 Jun-Jul;481-482:112788. doi: 10.1016/j.jim.2020.112788. Epub 2020 Apr 15.
Macrophages are one of the important cell types in the innate immune system that are present in various anatomical regions of the body and promote early control of pathogens. The relative proportion of macrophages in various lymphoid and non-lymphoid regions is small, and as such it is tedious to purify these cells to homogeneity. Culture of bone marrow precursors with macrophage colony-stimulating factor (M-CSF) results in their differentiation to macrophages, however this procedure results in low numbers of differentiated macrophages. Herein we reveal a new approach of generating increased numbers of differentiated macrophages from bone marrow precursors. We show that M-CSF delivered in a plate-bound form results in the differentiation of significantly more macrophages in comparison to soluble M-CSF. Furthermore, the macrophages differentiated with plate-bound M-CSF display increased metabolic activity and cell death following infection with pathogens.
巨噬细胞是先天免疫系统中的重要细胞类型之一,存在于身体的各个解剖区域,有助于早期控制病原体。巨噬细胞在各种淋巴和非淋巴区域的相对比例较小,因此要将这些细胞纯化至均一性非常繁琐。用巨噬细胞集落刺激因子(M-CSF)培养骨髓前体可诱导其分化为巨噬细胞,但该过程产生的分化巨噬细胞数量较少。在此,我们揭示了一种从骨髓前体中产生更多分化巨噬细胞的新方法。我们发现,与可溶性 M-CSF 相比,以板结合形式提供的 M-CSF 可诱导更多的巨噬细胞分化。此外,与板结合的 M-CSF 分化的巨噬细胞在感染病原体后显示出更高的代谢活性和细胞死亡。