Davies R, Legg R F, Neal G E
MRC Toxicology Unit, Carshalton, Surrey, UK.
Cell Biol Toxicol. 1990 Oct;6(4):353-63. doi: 10.1007/BF00120802.
The effects of TGF beta 1 on cell cycle events in a rat liver derived epithelial cell line (BL9) and in two in vitro transformants of this line were studied by flow cytometry. Using either ethidium bromide staining or the incorporation of bromodeoxyuridine to evaluate DNA synthesis it was shown that TGF beta 1 prevented the entry of G0/G1 phase BL9 cells into S phase. TGF beta 1 did not exert its inhibitory effect(s) on DNA synthesis by the modulation of early events in the cell cycle. The tumorigenic transformed BL9 cell lines gave contrasting responses to the effects of TGF beta 1. DNA synthesis in a BL9 cell line derived by transfection with an active N-ras oncogene was unaffected by TFG beta 1 and thus appeared refractory to its growth controlling effects. On the other hand cells from a BL9 cell line derived by in vitro transformation with activated aflatoxin B1 retained their sensitivity to the effects of TGF beta 1. Thus the loss of the inhibitory effect of TGF beta 1 on DNA synthesis is not obligatory for the malignant transformation of rat liver epithelial cells.
通过流式细胞术研究了转化生长因子β1(TGFβ1)对大鼠肝脏来源的上皮细胞系(BL9)及其两个体外转化细胞系细胞周期事件的影响。使用溴化乙锭染色或掺入溴脱氧尿苷来评估DNA合成,结果表明TGFβ1可阻止G0/G1期的BL9细胞进入S期。TGFβ1并非通过调节细胞周期早期事件来对DNA合成发挥抑制作用。致瘤性转化的BL9细胞系对TGFβ1的作用表现出不同的反应。用活性N-ras癌基因转染获得的BL9细胞系中的DNA合成不受TGFβ1影响,因此似乎对其生长控制作用具有抗性。另一方面,用活化的黄曲霉毒素B1进行体外转化获得的BL9细胞系中的细胞仍对TGFβ1的作用敏感。因此,TGFβ1对DNA合成抑制作用的丧失并非大鼠肝脏上皮细胞恶性转化所必需的。