Microcin E492, a channel-forming bacteriocin from Klebsiella pneumoniae, induces apoptosis in some human cell lines
Author
dc.contributor.author
Hetz Flores, Claudio
Author
dc.contributor.author
Bono Merino, María Rosa
Author
dc.contributor.author
Barros, Luis Felipe
Author
dc.contributor.author
Lagos Mónaco, Rosalba
Admission date
dc.date.accessioned
2019-01-29T13:47:48Z
Available date
dc.date.available
2019-01-29T13:47:48Z
Publication date
dc.date.issued
2002
Cita de ítem
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Proceedings of the National Academy of Sciences of the United States of America, Volumen 99, Issue 5, 2002, Pages 2696-2701
Identifier
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00278424
Identifier
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10.1073/pnas.052709699
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/159815
Abstract
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The cytotoxic effect of microcin E492, a low-molecular-mass channel-forming bacteriocin (7,887 Da) produced by a strain of Klebsiella pneumoniae, was characterized in HeLa cells. At low (5 microg/ml) and intermediate (10 microg/ml) concentrations, microcin E492 induced biochemical and morphological changes typical of apoptosis, such as cell shrinkage, DNA fragmentation, extracellular exposure of phosphatidylserine, caspase activation, and loss of mitochondrial membrane potential. Treatment with zVAD-fmk, a general caspase inhibitor, completely blocked the cytotoxic effect of this bacteriocin. At higher microcin concentrations (>20 microg/ml) a necrotic phenotype was observed. Induction of apoptosis by microcin E492 was associated with the release of calcium from intracellular stores, probably after microcin-triggered ion channel formation. Microcin E492 also presented a cytotoxic effect on Jurkat and RJ2.25 cells, but had no effect on KG-1 cells nor on a primary culture of human tonsil endothelial cells, suggesting that there is a specific interaction of the bacteriocin with components of the target cell surface. This report describes a bacteriocin that has the capacity to induce apoptosis in human cell lines.