Aksamit R R, Falk W, Leonard E J
J Immunol. 1981 Jun;126(6):2194-9.
Five mouse macrophage cell lines were tested for chemotaxis and phagocytosis. All 5 cell lines ingested sheep red cells coated with rabbit IgG anti-Forssman antibody and exhibited chemotaxis to endotoxin-activated mouse serum (EAMS) and lymphocyte-derived chemotactic factor. Two cell lines were tested for chemotaxis to f-Met-Leu-Phe and neither responded. Four of the cell lines (RAW264, RAW309CR, PU5-1R, and WR19M.1) exhibited chemotaxis to C5a. These cell lines displayed a 1- to 2-hr lag before migrating toward EAMS, and chemotaxis was dependent upon cell density. When fewer than 10(3) cells were present per mm2 of filter surface, less than 10% of the cells migrated; however, at a density of 5 X 10(3) cells/mm2 50 to 70% of the cells migrated. WEHI-3 differed from the other cell lines in that there was no chemotaxis to C5a, migration to EAMS did not have a detectable lag, and there was no cell density dependence for chemotaxis. Comparison of these chemotactic properties with those reported in the literature for mouse macrophages and monocytes suggests that RAW264, RAW309CR, PU5-1R, and WR19M.1 have properties that are similar to those of mouse resident macrophages, whereas WEHI-3 may have some of the properties of mouse monocytes.
对五种小鼠巨噬细胞系进行趋化性和吞噬作用测试。所有这五种细胞系均摄取了包被有兔IgG抗福斯曼抗体的绵羊红细胞,并对内毒素激活的小鼠血清(EAMS)和淋巴细胞衍生的趋化因子表现出趋化性。测试了两种细胞系对f-Met-Leu-Phe的趋化性,均无反应。其中四种细胞系(RAW264、RAW309CR、PU5-1R和WR19M.1)对C5a表现出趋化性。这些细胞系在向EAMS迁移前有1至2小时的延迟,趋化性取决于细胞密度。当每平方毫米滤膜表面的细胞数少于10³个时,迁移的细胞不到10%;然而,当细胞密度为5×10³个/平方毫米时,50%至70%的细胞发生迁移。WEHI-3与其他细胞系不同,它对C5a无趋化性,向EAMS的迁移没有可检测到的延迟,且趋化性不存在细胞密度依赖性。将这些趋化特性与文献中报道的小鼠巨噬细胞和单核细胞的趋化特性进行比较表明,RAW264、RAW309CR、PU5-1R和WR19M.1具有与小鼠常驻巨噬细胞相似的特性,而WEHI-3可能具有一些小鼠单核细胞的特性。