Sawai M, Takase K, Teraoka H, Tsukada K
Department of Pathological Biochemistry, Medical Research Institute, Medical and Dental University, Japan.
Exp Cell Res. 1990 Mar;187(1):4-10. doi: 10.1016/0014-4827(90)90108-m.
Proliferation of human B- and T-lymphoid cell lines including Raji and Akata cells was found to be arrested at the G1 stage in the cell cycle by dimethyl sulfoxide (DMSO). The G1 arrest by DMSO occurred gradually and was completed within 96 h after addition of 1.5% DMSO concomitantly with a decrease in growth rate. Progression of G1-phase cells containing a larger amount of RNA into S-phase began 9-12 h after removal of DMSO. At 24 h, the DNA pattern of the cell cycle was similar to that of nontreated log-phase cells. The expression of six differentiation markers on the lymphoid cells was not appreciably changed by treatment with DMSO. On the other hand, the expression of transferrin receptor (one of the growth-related markers) on G1-phase cells 96 h after addition of DMSO was decreased to one-fourth that on log-phase cells and was completely restored 24 h after removal of DMSO. These results indicate that DMSO, known as an inducer of differentiation in several myeloid cell lines, acts as an agent inducing G1 arrest in the cell cycle of the lymphoid cells.
已发现包括Raji和Akata细胞在内的人B淋巴细胞系和T淋巴细胞系的增殖在细胞周期的G1期被二甲基亚砜(DMSO)阻滞。DMSO对G1期的阻滞是逐渐发生的,在加入1.5% DMSO后96小时内完成,同时生长速率下降。含有大量RNA的G1期细胞在去除DMSO后9 - 12小时开始进入S期。在24小时时,细胞周期的DNA模式与未处理的对数期细胞相似。用DMSO处理后,淋巴细胞上六种分化标志物的表达没有明显变化。另一方面,加入DMSO 96小时后,G1期细胞上转铁蛋白受体(生长相关标志物之一)的表达降至对数期细胞的四分之一,并在去除DMSO 24小时后完全恢复。这些结果表明,DMSO在几种髓系细胞系中作为分化诱导剂,在淋巴细胞的细胞周期中充当诱导G1期阻滞的因子。