Carvajal R E, Maldonado G
Cell Biol Int Rep. 1986 Feb;10(2):101-7. doi: 10.1016/0309-1651(86)90093-7.
The non-immune mechanisms of recognition of self and non-self substances by macrophages has not yet been clarified. In this work, we report the ability of mouse peritoneal macrophages to attach to and phagocytize in vitro autologous and homologous erythrocytes in proportions as high as those for certain heterologous red blood cells. This ability was abrogated by autologous or homologous serum but not by heterologous serum or a serum-free supplement. This effect of serum was dose dependent and did not affect the phagocytosis of homologous "old" red cells. Procedures for the identification of this serum factor indicated that it was dialyzable (10 kD cut off) and was excluded by filtration in Sephadex G-25. We conclude that this finding supports the possibility that macrophages do not selectively phagocytize foreign particles or senescent cells but, rather, that they do phagocytize all particles or cells indiscriminately and this serum factor may prevent phagocytosis of normal self cells.
巨噬细胞识别自身和非自身物质的非免疫机制尚未阐明。在这项研究中,我们报告了小鼠腹腔巨噬细胞在体外附着并吞噬自体和同源红细胞的能力,其比例与某些异源红细胞的比例一样高。这种能力被自体或同源血清消除,但不被异源血清或无血清补充剂消除。血清的这种作用是剂量依赖性的,并且不影响同源“衰老”红细胞的吞噬作用。鉴定这种血清因子的程序表明它是可透析的(截留分子量10 kD),并且在Sephadex G-25中过滤时被截留。我们得出结论,这一发现支持了巨噬细胞不会选择性吞噬外来颗粒或衰老细胞,而是会不加区分地吞噬所有颗粒或细胞的可能性,并且这种血清因子可能会阻止正常自身细胞的吞噬作用。