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dc.contributor.authorBahi i Pla, Núria
dc.contributor.authorZhang, Jisheng
dc.contributor.authorLlovera i Tomàs, Marta
dc.contributor.authorBallester, Manel
dc.contributor.authorComella i Carnicé, Joan Xavier
dc.contributor.authorSanchis, Daniel
dc.date.accessioned2022-03-03T13:29:44Z
dc.date.available2022-03-03T13:29:44Z
dc.date.issued2006
dc.identifier.issn0021-9258
dc.identifier.issn1083-351X
dc.identifier.urihttp://hdl.handle.net/10459.1/73162
dc.description.abstractDifferentiated cardiomyocytes are resistant to caspase-dependent cell death; however, the mechanisms involved are still uncertain. We previously reported that low Apaf1 expression partially accounts for cardiomyocyte resistance to apoptosis. Here, we extend the knowledge on the molecular basis of cardiac resistance to caspase activation by showing that the whole caspase-dependent pathway is silenced during heart development. Experimental ischemia triggers caspase activation in embryonic cardiomyocytes and proliferating fibroblasts, but not in neonatal and adult cardiomyocytes. Ischemia induces the release of the proapoptotic factors cytochrome c, truncated-AIF, and EndoG from mitochondria in postnatal cardiomyocytes in the absence of caspase activation. On the one hand, lentiviral-driven knockdown of EndoG shows that this gene is essential for ischemia-induced DNA degradation in neonatal cardiomyocytes, but not in proliferating fibroblasts; on the other hand, the AIF gene is essential for high molecular DNA cleavage in fibroblasts, but not in postmitotic cardiomyocytes, where it plays a prosurvival role during reoxygenation. These results show the switch from caspase-dependent to caspase-independent death pathways after cardiac cell differentiation, and disclose the relevance of EndoG in the caspase-independent DNA processing of differentiated cardiomyocytes.ca_ES
dc.language.isoengca_ES
dc.publisherAmerican Society for Biochemistry and Molecular Biologyca_ES
dc.publisherElsevierca_ES
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1074/jbc.M601025200ca_ES
dc.relation.ispartofJournal of Biological Chemistry (JBC), 2006, vol. 281, núm. 32, p. 22943-22952ca_ES
dc.rightscc-by (c)The American Society for Biochemistry and Molecular Biology, 2006ca_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleSwitch from caspase-dependent to caspase-independent death during heart development: essential role of endonuclease G in ischemia-induced DNA processing of differentiated cardiomyocytesca_ES
dc.typeinfo:eu-repo/semantics/articleca_ES
dc.identifier.idgrec009998
dc.type.versioninfo:eu-repo/semantics/publishedVersionca_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccessca_ES
dc.identifier.doihttps://doi.org/10.1074/jbc.M601025200


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cc-by (c)The American Society for Biochemistry and Molecular Biology, 2006
Except where otherwise noted, this item's license is described as cc-by (c)The American Society for Biochemistry and Molecular Biology, 2006