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Glucocorticoid/oxysterol-induced DNA lysis in human leukemic cells
被引:17
|作者:
Johnson, BH
[1
]
AyalaTorres, S
[1
]
Chan, LNL
[1
]
ElNaghy, M
[1
]
Thompson, EB
[1
]
机构:
[1] UNIV TEXAS,MED BRANCH,DEPT HUMAN BIOL CHEM & GENET,GALVESTON,TX 77555
来源:
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY
|
1997年
/
61卷
/
1-2期
关键词:
D O I:
10.1016/S0960-0760(96)00256-7
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Both glucocorticoids and oxysterols, steroids with quite different known transduction pathways, cause the death of lymphoid cells. Dual TUNEL/propidium iodide assays on sensitive human leukemic CEM-C7 clones treated with either steroid were clearly positive by 48 h, consistent with apoptosis. Both steroids evoked two distinctive types of DNA lysis: cleavage into large fragments of several different sizes and the classic ''ladders'', multiples of similar to 200 base pairs. Conventional gel electrophoresis showed that a small proportion of total DNA had undergone laddering 36-48 h after treatment with glucocorticoid or 24 h after oxysterol exposure. On field inversion gel electrophoresis of cellular DNA both steroids caused an increase in an array of large DNA fragments <50 kb in size. A 50 kb fragment appeared 36 h after treatment with either steroid, but only oxysterol treatment caused a significant increase in a 300 kb fragment. Oxysterol treatment did not result in DNA fragmentation in the resistant M10R5 subclone, which retained sensitivity to glucocorticoids. We conclude that glucocorticoids and oxysterols kill these cells with similar, but not identical, patterns of DNA lysis which occur just before or concomitant with the onset of cell death. (C) 1997 Elsevier Science Ltd.
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页码:35 / 45
页数:11
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