Ono M, Ando M, Shimada T, Furuno K, Kato K, Kuwano M
J Biochem. 1983 Nov;94(5):1493-503.
Chloroquine-resistant (CQr) clones (CQ-21 and CQ-22) have been isolated from mutagenized hamster lung V79 cells by exposing the cells to a high dose of chloroquine. CQ-21 and CQ-22 showed about 3-fold higher resistance to chloroquine than the parental V79 cells, and they showed specific cross-resistance to another amine, NH4Cl, which is also concentrated in lysosomes. CQr clone showed no cross-resistance to other unrelated agents. Chloroquine-induced inhibition of [125I]ricin internalization was observed in both cell lines at neutral pH, but the inhibition of uptake was less in the variant. Also, the degradation of endogenous protein was slowed in the mutant; further, treatment of cells with 30 micrograms/ml of chloroquine inhibited the degradation of endogenous proteins in the parental V79, but not in CQ-22 cells. Similar levels of acid phosphatase, beta-glucuronidase and cathepsin D were observed in V79 and CQ-22 cells, but the level of cathepsin B was lower in the mutant. Electron microscopy showed an increased number of electron-dense bodies, possibly autophagosomes/lysosomes, in the mutant cells grown for 4 days with 5 micrograms/ml of chloroquine. Similar aberrant structures were observed in the parental V79 cells treated for only 3 h with 5 micrograms/ml of chloroquine.
通过将细胞暴露于高剂量氯喹,从诱变的仓鼠肺V79细胞中分离出氯喹抗性(CQr)克隆(CQ - 21和CQ - 22)。CQ - 21和CQ - 22对氯喹的抗性比亲代V79细胞高约3倍,并且它们对另一种也集中在溶酶体中的胺NH4Cl表现出特异性交叉抗性。CQr克隆对其他无关药物没有交叉抗性。在中性pH条件下,两种细胞系中均观察到氯喹诱导的[125I]蓖麻毒素内化抑制,但变体中的摄取抑制作用较小。此外,突变体中内源性蛋白质的降解减慢;此外,用30微克/毫升氯喹处理细胞可抑制亲代V79细胞中内源性蛋白质的降解,但对CQ - 22细胞无效。在V79和CQ - 22细胞中观察到相似水平的酸性磷酸酶、β - 葡萄糖醛酸酶和组织蛋白酶D,但突变体中组织蛋白酶B的水平较低。电子显微镜显示,在含有5微克/毫升氯喹培养4天的突变体细胞中,电子致密体(可能是自噬体/溶酶体)的数量增加。在用5微克/毫升氯喹仅处理3小时的亲代V79细胞中也观察到类似的异常结构。