Nanno M, Shimizu-Takeda T, Mike A, Ohwaki M, Togashi Y, Suzuki R, Kumagai K, Mutai M
Yakult Central Institute for Microbiological Research, Tokyo, Japan.
J Leukoc Biol. 1989 Aug;46(2):89-95. doi: 10.1002/jlb.46.2.89.
Heat-killed Lactobacillus casei YIT9018 (LC9018), when administered intravenously to normal mice, induced increase in Mac-1+ cells and Mac-2+ cells but not in Mac-3+ cells in spleen. The number of both populations changed in the same time course and was maximal 14 d after the administration. To know the effect of LC9018 on hematopoietic progenitor level, we examined the number of macrophage colony-forming cells (M-CFC), granulocyte-macrophage CFC (GM-CFC), and colony-forming units in spleen (CFU-S) in bone marrow 3 d after the administration. LC9018 stimulated the proliferation of M-CFC but not that of GM-CFC and CFU-S. LC9018-induced M-CFC were similar to normal M-CFC in dependence on macrophage colony-stimulating factor (M-CSF) and buoyant density. M-CFC-derived macrophages cultured in the presence of M-CSF expressed Mac-1 and Mac-2 but not Mac-3. They showed cytotoxic activity against syngenic tumor cells, Meth A, via direct contact, when assayed by using an in vitro colony inhibition assay or an in vivo Winn test. These results indicate that LC9018 stimulates the proliferation of cytotoxic macrophage progenitors in bone marrow and induces their differentiation in spleen. These effects may be one of the ways in which LC9018 suppresses tumor growth.
将热灭活的干酪乳杆菌YIT9018(LC9018)静脉注射给正常小鼠后,可诱导脾脏中Mac-1+细胞和Mac-2+细胞数量增加,但不会使Mac-3+细胞数量增加。这两种细胞群体的数量在相同的时间进程中发生变化,给药后14天达到最大值。为了解LC9018对造血祖细胞水平的影响,我们在给药后3天检测了骨髓中巨噬细胞集落形成细胞(M-CFC)、粒细胞-巨噬细胞集落形成细胞(GM-CFC)以及脾脏集落形成单位(CFU-S)的数量。LC9018刺激了M-CFC的增殖,但未刺激GM-CFC和CFU-S的增殖。LC9018诱导产生的M-CFC在对巨噬细胞集落刺激因子(M-CSF)的依赖性和浮力密度方面与正常M-CFC相似。在M-CSF存在的情况下培养的M-CFC来源的巨噬细胞表达Mac-1和Mac-2,但不表达Mac-3。当通过体外集落抑制试验或体内温氏试验进行检测时,它们通过直接接触对同基因肿瘤细胞Meth A表现出细胞毒性活性。这些结果表明,LC9018刺激骨髓中细胞毒性巨噬细胞祖细胞的增殖,并诱导其在脾脏中分化。这些作用可能是LC9018抑制肿瘤生长的方式之一。