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dc.contributor.authorZheng, Jieen
dc.date2008-10-27 00:24:02.204
dc.date.accessioned2008-10-27T18:01:10Z
dc.date.available2008-10-27T18:01:10Z
dc.date.issued2008-10-27T18:01:10Z
dc.identifier.urihttp://hdl.handle.net/1974/1562
dc.descriptionThesis (Ph.D, Biology) -- Queen's University, 2008-10-27 00:24:02.204en
dc.description.abstractSeveral genes involved in the regulation of apoptosis can influence longevity. Although observations in several different systems imply that apoptosis and aging are closely linked, the relationship between the two remains largely unknown. In this study, Drosophila melanogaster was used as a model organism to explore the relationship between aging and apoptosis regulation. Apoptosis was investigated using two apoptotic hallmarks: caspase activity and DNA fragmentation. The results showed that apoptosis occured in adult flies at all ages and the changes in apoptosis associated with aging were linked to physiological age and were tissue-specific. During normal fly aging, apoptosis increased gradually within the muscle and was activated in the fat of old flies. However, neither of the two apoptotic signs were shown in the nervous system. The analysis of the apoptotic response to starvation and oxidative stress suggested that the increased apoptosis in muscle resulted from the accumulation of oxidative damage associated with aging. Once the presence of apoptosis during Drosophila aging was confirmed, the expression of anti-apoptotic genes was manipulated in specific tissues to examine the impact of a localized alternation of apoptosis on aging. The overexpression of anti-apoptotic genes in muscle extended Drosophila mean and maximum life span up to 99% and 65%, respectively. This extension was mediated by apoptosis inhibition using the detection of caspase activity and DNA fragmentation. In addition, the long-lived animals exhibited increased resistance to oxidative stress and preserved flight ability. Overall this study establishes that muscle apoptosis limits life span and participates in sarcopenia. This finding may have applications in the development of interventions to improve the life quality of elderly human.en
dc.format.extent22910184 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoengen
dc.relation.ispartofseriesCanadian thesesen
dc.rightsThis publication is made available by the authority of the copyright owner solely for the purpose of private study and research and may not be copied or reproduced except as permitted by the copyright laws without written authority from the copyright owner.en
dc.subjectApoptosisen
dc.subjectAgingen
dc.subjectDrosophilaen
dc.subjectCaspaseen
dc.titleApoptosis and Aging in Drosophilaen
dc.typethesisen
dc.description.degreePhDen
dc.contributor.supervisorSeroude, Laurenten
dc.contributor.departmentBiologyen
dc.degree.grantorQueen's University at Kingstonen


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