Takahashi T, Suzuki A, Ichiba S, Okuno Y, Sugiyama H, Imura H, Nakamura K, Iho S, Hoshino T
Second Department of Internal Medicine, Faculty of Medicine, Kyoto University, Japan.
Int J Hematol. 1991 Feb;54(1):57-63.
1,25-Dihydroxyvitamin D-3 (1,25(OH)2D3) suppresses colony formation of normal human granulocyte macrophage progenitors (CFU-GM) and induces differentiation of colonies into monocyte macrophages in vitro. We examined whether or not the target cell of 1,25(OH)2D3 is only CFU-GM in the suppression and differentiation of colonies by the agent. Reduction of colony counts was observed only when 1,25(OH)2D3 was added to CFU-GM cultures at days 0 or 3, and after day 5 the agent did not affect the colony count. However, the delayed addition of 1,25(OH)2D3 elevated the proportion of granulocyte macrophage (GM) or macrophage (M) colonies even after 5 days of culture. We confirmed transformation of day 11 colony cells into macrophages by 1,25(OH)2D3 during the following 3 days' culture period based on serial observations of single colonies. Day 11 colonies contained very few CFU-GM and their most immature cells were promyelocytes. Short-term exposure to 1,25(OH)2D3 (4 h) of bone marrow cells, which had been precultured for 24 to 72 h with a purified granulocyte-colony stimulating factor caused a reduction of colony counts but did not elevate the proportions of GM or M colonies. These results indicate that 1,25(OH)2D3 inhibits the growth of CFU-GM itself and induces differentiation into macrophages at the progeny level (probably promyelocytes) and not at the level of CFU-GM.
1,25 - 二羟基维生素D - 3(1,25(OH)2D3)在体外可抑制正常人粒细胞巨噬细胞祖细胞(CFU - GM)的集落形成,并诱导集落分化为单核巨噬细胞。我们研究了在该因子对集落的抑制和分化作用中,1,25(OH)2D3的靶细胞是否仅为CFU - GM。仅在第0天或第3天向CFU - GM培养物中添加1,25(OH)2D3时,才观察到集落计数减少,而在第5天后该因子对集落计数没有影响。然而,即使在培养5天后,延迟添加1,25(OH)2D3仍会提高粒细胞巨噬细胞(GM)或巨噬细胞(M)集落的比例。基于对单个集落的连续观察,我们证实了在接下来3天的培养期内,第11天的集落细胞可被1,25(OH)2D3转化为巨噬细胞。第11天的集落中CFU - GM极少,其最不成熟的细胞为早幼粒细胞。用纯化的粒细胞集落刺激因子预培养24至72小时的骨髓细胞短期暴露于1,25(OH)2D3(4小时)会导致集落计数减少,但不会提高GM或M集落的比例。这些结果表明,1,25(OH)2D3抑制CFU - GM本身的生长,并在子代水平(可能是早幼粒细胞)而非CFU - GM水平诱导其分化为巨噬细胞。