Grosse Y, Baudrimont I, Castegnaro M, Betbeder A M, Creppy E E, Dirheimer G, Pfohl-Leszkowicz A
Ecole Nationale Supérieure Agronomique, Toulouse, France.
Chem Biol Interact. 1995 Mar 30;95(1-2):175-87. doi: 10.1016/0009-2797(94)03359-5.
Monkey kidney cells (named Vero cells) were incubated with increasing doses of ochratoxin A (10-100 microM). The inhibiting concentration 50% (IC50) on protein synthesis was about 14 microM in the presence of 5% fetal calf serum and 37 microM in the presence of 10% fetal calf serum. Some metabolites of ochratoxin A, including the chlorinated dihydroisocoumarin moiety of OTA (OT alpha), 4-[S]-hydroxy-OTA and 4-[R]-hydroxy-OTA were detected by HPLC in the mixture of cell homogenate after a 24 h incubation with 10 and 25 microM of OTA. Using the 32P-postlabelling method, several DNA-adducts, similar to those formed in mouse kidney after OTA treatment, were detected in monkey kidney cells. Thus, Vero cells are suitable for genotoxic and cytotoxic studies in relation to the metabolism of nephrotoxic xenobiotics such as OTA.
将猴肾细胞(命名为Vero细胞)与递增剂量的赭曲霉毒素A(10 - 100微摩尔)一起孵育。在5%胎牛血清存在的情况下,对蛋白质合成的半数抑制浓度(IC50)约为14微摩尔,在10%胎牛血清存在的情况下为37微摩尔。在用10和25微摩尔OTA孵育24小时后,通过高效液相色谱法在细胞匀浆混合物中检测到了赭曲霉毒素A的一些代谢产物,包括OTA的氯化二氢异香豆素部分(OTα)、4 - [S] - 羟基 - OTA和4 - [R] - 羟基 - OTA。使用32P后标记法,在猴肾细胞中检测到了几种与OTA处理后小鼠肾脏中形成的类似的DNA加合物。因此,Vero细胞适用于与肾毒性外源性物质(如OTA)代谢相关的遗传毒性和细胞毒性研究。