Langdon S P, Richards F M, Hickman J A
Cancer Research Campaign Experimental Chemotherapy Group, Aston University, Birmingham, U.K.
Leuk Res. 1988;12(3):211-6. doi: 10.1016/0145-2126(88)90138-5.
The relationship between the N-methylformamide (NMF)-induced differentiation of HL-60 human promyelocytic leukemia cells, to myeloid cells, and their proliferative potential was determined in suspension culture. Continuous incubation with 170 mM NMF induced 70% of cells to differentiate after 2-2.5 cell divisions, whether or not cells were replenished with fresh medium and serum. 100 mM NMF induced significant levels of differentiation only when cells were allowed to reach a plateau of growth, and this was prevented by replenishment of the medium and serum. Under these conditions of "re-feeding", the cells could be made to undergo greater than 10 cell divisions, and differentiated only when they were allowed to reach a plateau in their growth. The data suggests that NMF may induce differentiation only when the proliferative potential of the cells is limited, either by the drug itself or by the conditions of growth.
在悬浮培养中确定了N-甲基甲酰胺(NMF)诱导HL-60人早幼粒细胞白血病细胞向髓样细胞分化与其增殖潜能之间的关系。无论是否用新鲜培养基和血清补充细胞,用170 mM NMF连续孵育2-2.5个细胞周期后可诱导70%的细胞分化。仅当细胞达到生长平台期时,100 mM NMF才诱导显著水平的分化,而补充培养基和血清可阻止这种分化。在“再喂养”的这些条件下,细胞可进行超过10个细胞周期的分裂,并且仅当它们达到生长平台期时才分化。数据表明,NMF可能仅在细胞的增殖潜能受到限制时才诱导分化,这种限制要么是由药物本身造成,要么是由生长条件造成。