Bhalla K N, Li G R, Grant S, Cole J T, MacLaughlin W W, Volsky D J
Division of Hematology/Oncology, Medical University of South Carolina, Charleston 29425.
AIDS. 1990 May;4(5):427-31. doi: 10.1097/00002030-199005000-00008.
We examined in vitro the effect of high, but clinically achievable and non-toxic, concentrations of 2'-deoxycytidine (dCyd) (greater than or equal to 100 mumols/l on the metabolism and cytotoxicity of 2',3'-dideoxycytidine (DDC) in normal human bone marrow mononuclear cells (BMMCs) and a cultured T-lymphocyte (HUT-102) cell line. Colony formation in semi-solid medium by bone marrow progenitor cells (CFU-GM and CFU-GEMM) was significantly protected by dCyd against the cytotoxic effects of high doses of DDC. In contrast, in HIV-infected HUT-102 cells, anti-HIV effect of DDC (10 mumols/l) was preserved in the presence of 100 mumols/l dCyd but partially reversed by higher levels of dCyd. dCyd reduced the generation of DDC triphosphate (DDC-TP) relative to dCyd triphosphate (dCTP) pools to a significantly greater extent in BMMCs versus HUT-102 cells. This might explain dCyd-mediated abrogation of DDC cytotoxicity against marrow progenitor cells with relative preservation of its anti-HIV-1 activity in HUT-102 cells.
我们在体外研究了高浓度但临床上可达到且无毒的2'-脱氧胞苷(dCyd)(≥100μmol/L)对正常人骨髓单个核细胞(BMMCs)和培养的T淋巴细胞(HUT-102)细胞系中2',3'-二脱氧胞苷(DDC)代谢及细胞毒性的影响。骨髓祖细胞(CFU-GM和CFU-GEMM)在半固体培养基中的集落形成受到dCyd的显著保护,免受高剂量DDC的细胞毒性作用。相比之下,在感染HIV的HUT-102细胞中,100μmol/L dCyd存在时DDC(10μmol/L)的抗HIV作用得以保留,但更高水平的dCyd会使其部分逆转。与HUT-102细胞相比,dCyd在BMMCs中使DDC三磷酸(DDC-TP)相对于胞苷三磷酸(dCTP)池的生成减少的程度显著更大。这可能解释了dCyd介导的对骨髓祖细胞DDC细胞毒性的消除,同时其在HUT-102细胞中的抗HIV-1活性得以相对保留。