dc.creatorCarbonell, GV
dc.creatorFalcon, R
dc.creatorYamada, AT
dc.creatorda Fonseca, BAL
dc.creatorYano, T
dc.date2004
dc.dateJAN-FEB
dc.date2014-11-18T16:29:28Z
dc.date2015-11-26T17:52:33Z
dc.date2014-11-18T16:29:28Z
dc.date2015-11-26T17:52:33Z
dc.date.accessioned2018-03-29T00:36:02Z
dc.date.available2018-03-29T00:36:02Z
dc.identifierResearch In Microbiology. Elsevier Science Bv, v. 155, n. 1, n. 25, n. 30, 2004.
dc.identifier0923-2508
dc.identifierWOS:000189308500004
dc.identifier10.1016/j.resmic.2003.09.009
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/82390
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/82390
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/82390
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1290278
dc.descriptionIn the present work, in vitro assays were used to investigate the toxicity of Serratia marcescens cytotoxin in cultured Chinese hamster ovary (CHO) cells. The time necessary to detect cellular alterations such as the onset of apoptosis, the perturbation of mitochondrial function, and cytoskeletal changes was assessed. The internalization of the cytotoxin by CHO cells was also examined. Within 10-15 min of exposure to cytotoxin, CHO cells became round, the nucleus shrank, the chromatin became more compact, and cytoplasmic blebs appeared on the cell surface. TUNEL (TdT-mediated dUTP nick end labeling) and propidium iodide staining identified some nuclei with fragmented DNA, and electrophoresis of CHO cell DNA obtained after 30-min exposure to S. marcescens toxin showed a pattern of DNA fragments typically associated with apoptosis. The cells also lost their characteristic actin organization within 10 min of exposure to cytotoxin. Lactate dehydrogenase leakage was detected after 20-min exposure to the cytotoxin and increased with time thereafter. Concomitantly, there was a time-dependent reduction in mitochondrial activity. Fluorescein-labeled S. marcescens cytotoxin was detected only on the surface of CHO cells, even after 30-min exposure to the toxin. These results show that there was no internalization of the toxin by CHO cells, and that, once bound to the cell surface, the toxin was able to induce changes in intracellular metabolism and to trigger cell death by apoptosis. (C) 2003 Elsevier SAS. All rights reserved.
dc.description155
dc.description1
dc.description25
dc.description30
dc.languageen
dc.publisherElsevier Science Bv
dc.publisherAmsterdam
dc.publisherHolanda
dc.relationResearch In Microbiology
dc.relationRes. Microbiol.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectSerratia marcescens
dc.subjectcytotoxin
dc.subjectapoptosis
dc.subjectvirulence factors
dc.subjectCells
dc.subjectApoptosis
dc.subjectDna
dc.titleMorphological and intracellular alterations induced by Serratia marcescens cytotoxin
dc.typeArtículos de revistas


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