细胞凋亡
有丝分裂
程序性细胞死亡
生物
DNA断裂
细胞毒性T细胞
半胱氨酸蛋白酶
相间
细胞生物学
分子生物学
生物化学
体外
作者
Susan L. Mooberry,Lizette Busquets,Georgia Tien
标识
DOI:10.1002/(sici)1097-0215(19971104)73:3<440::aid-ijc20>3.0.co;2-f
摘要
The ability of cryptophycin 1, a new potent cytotoxic antimicrotubule agent, to initiate apoptosis was studied. Treatment of cells with cryptophycin 1 (50 pM) rapidly caused morphological changes consistent with the induction of apoptosis. DNA strand breakage and fragmentation of the DNA into oligonucleosome-sized fragments was observed, and this coincided with the loss of cellular DNA. Activation of the cysteine protease CPP32 (caspase 3, YAMA, apopain), a member of the ICE/CED-3-like protease family of apoptosis effectors, was consistent with the execution of cell death by a coordinated sequence of events. Low concentrations of cryptophycin 1 caused mitotic arrest with the formation of abnormal mitotic spindles without affecting interphase microtubule structures. Unlike other microtubule active agents, cryptophycin-induced mitotic arrest persisted for only a brief period before the onset of apoptosis. There was no evidence of release from G2/M cell cycle arrest. Our results show that low concentrations of cryptophycin 1 (50 pM) initiated cell death consistent with apoptosis. These data suggest that the cytotoxic effects of cryptophycin 1 are due in part to its ability to initiate apoptosis rapidly. Int. J. Cancer 73:440–448, 1997. © 1997 Wiley-Liss, Inc.
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