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J Biol Chem ; 272(48): 30567-76, 1997 Nov 28.
Article in English | MEDLINE | ID: mdl-9374553

ABSTRACT

Little is known about the mechanisms of suppression of apoptosis. We have addressed the novel possibility that the level of intracellular K+ regulates the apoptotic process by controlling the activity of death enzymes. We show that K+, at normal intracellular levels, inhibits both apoptotic DNA fragmentation and caspase-3(CPP32)-like protease activation, suggesting that intracellular K+ loss must occur early during apoptosis. Direct measurement of K+ by inductively coupled plasma/mass spectrometry and flow cytometry indicates a major decrease in intracellular K+ concentration in the apoptotic cell. Flow cytometric analysis revealed that caspase and nuclease activity were restricted to the subpopulation of cells with reduced K+. Disruption of the natural K+ electrochemical gradient suppressed the activity of both caspase and nuclease independent of the mode of activation of the apoptotic inducing agent, demonstrating that a decrease in intracellular K+ concentration is a necessary, early event in programmed cell death.


Subject(s)
Apoptosis , Caspases , Lymphocytes/cytology , Potassium/physiology , Animals , Apoptosis/drug effects , Caspase 3 , Cysteine Endopeptidases/physiology , Cytoplasm/physiology , DNA Fragmentation , Deoxyribonucleases/antagonists & inhibitors , Deoxyribonucleases/metabolism , Dexamethasone/pharmacology , Enzyme Activation/drug effects , Enzyme Precursors/metabolism , Glucocorticoids/pharmacology , Lymphocytes/enzymology , Male , Nucleosomes/metabolism , Potassium/pharmacology , Rats , Rats, Sprague-Dawley , Thymus Gland/cytology
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