Takanashi M, Motoji T, Masuda M, Oshimi K, Mizoguchi H
Department of Medicine, Tokyo Women's Medical College, Japan.
Leuk Res. 1993 Mar;17(3):217-22. doi: 10.1016/0145-2126(93)90004-5.
The effects of leukemia inhibitory factor (LIF) and interleukin 6 (IL-6) on blast progenitors from acute myeloblastic leukemia (AML) were examined using a blast colony assay in a serum-free culture system. LIF and IL-6 stimulated colony growth in 2 and 5, respectively, of 11 cases studied. The simultaneous addition of LIF with granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin 3 (IL-3) or IL-6 produced a statistically significant increase of colony numbers in 3, 6 and 7 of 11 cases, respectively. Numbers of colonies increased significantly when IL-6 was added simultaneously with GM-CSF or IL-3 in 5 and 4 of 11 cases, respectively. LIF or IL-6 used in the primary culture did not significantly change the numbers of secondary colonies compared to GM-CSF. Previous exposure to LIF and IL-6 did not alter cellular phenotype or morphology, indicating that LIF and IL-6 did not induce the differentiation of fresh AML blasts.
在无血清培养系统中,使用原始细胞集落测定法检测了白血病抑制因子(LIF)和白细胞介素6(IL-6)对急性髓细胞白血病(AML)原始祖细胞的影响。在所研究的11例病例中,LIF和IL-6分别刺激了其中2例和5例的集落生长。LIF与粒细胞-巨噬细胞集落刺激因子(GM-CSF)、白细胞介素3(IL-3)或IL-6同时添加时,分别在11例中的3例、6例和7例中使集落数量有统计学意义的增加。IL-6与GM-CSF或IL-3同时添加时,分别在11例中的5例和4例中使集落数量显著增加。与GM-CSF相比,原代培养中使用的LIF或IL-6并未显著改变二代集落的数量。先前暴露于LIF和IL-6并未改变细胞表型或形态,表明LIF和IL-6并未诱导新鲜AML原始细胞的分化。