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Apoptotic cell death induced by inhibitors of energy conservation Bcl-2 inhibits apoptosis downstream of a fall of ATP level
被引:49
|作者:
Marton, A
Mihalik, R
Bratincsak, A
Adleff, V
Petak, I
Vegh, M
Bauer, PI
Krajcsi, P
机构:
[1] SEMMELWEIS UNIV MED, SCH MED, DEPT MED BIOCHEM, H-1444 BUDAPEST, HUNGARY
[2] I INST PATHOL & EXPT CANC RES, BUDAPEST, HUNGARY
[3] EGIS PHARMACEUT, DIV BIOL RES, H-1475 BUDAPEST, HUNGARY
来源:
关键词:
apoptosis;
ATP;
energy conservation;
Bcl-2;
metabolic regulation;
D O I:
10.1111/j.1432-1033.1997.0467a.x
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:
Energy charge controls intermediary metabolism and cellular regulation. Here we show that inhibition of energy conservation at the level of glucose uptake, glycolysis, citric acid cycle: and oxidative phosphorylation induces cell death, leading to fragmentation of DNA into an oligonucleosomal ladder and morphological changes typical for apoptosis. Bcl-2, the prototype of oncogenes that suppress cell death, efficiently inhibits apoptosis induced by metabolic inhibitors. Bcl-2 does not antagonize the inhibitory potential of mitochondrial inhibitors, and cannot prevent or delay the decrease of the cellular ATP level subsequent to metabolic inhibition. Thus, we propose that Bcl-2 blocks apoptosis at a point downstream of the collapse of the cellular-energy homeostasis.
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页码:467 / 475
页数:9
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