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Role of mitochondrial function in cell death and body metabolism

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dc.contributor.author이명식-
dc.date.accessioned2017-10-26T07:24:21Z-
dc.date.available2017-10-26T07:24:21Z-
dc.date.issued2016-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/151987-
dc.description.abstractMitochondria are the key players in apoptosis and necrosis. Mitochondrial DNA (mtDNA)-depleted r0 cells were resistant to diverse apoptosis inducers such as TNF-alpha, TNFSF10, staurosporine and p53. Apoptosis resistance was accompanied by the absence of mitochondrial potential loss or cytochrome c translocation. r0 cells were also resistant to necrosis induced by reactive oxygen species (ROS) donors due to upregulation of antioxidant enzymes such as manganese superoxide dismutase. Mitochondria also has a close relationship with autophagy that plays a critical role in the turnover of senescent organelles or dysfunctional proteins and may be included in 'cell death' category. It was demonstrated that autophagy deficiency in insulin target tissues such as skeletal muscle induces mitochondrial stress response, which leads to the induction of FGF21 as a 'mitokine' and affects the whole body metabolism. These results show that mitochondria are not simply the power plants of cells generating ATP, but are closely related to several types of cell death and autophagy. Mitochondria affect various pathophysiological events related to diverse disorders such as cancer, metabolic disorders and aging.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherFrontiers in Bioscience-
dc.relation.isPartOfFRONTIERS IN BIOSCIENCE-LANDMARK-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAnimals-
dc.subject.MESHApoptosis/physiology-
dc.subject.MESHAutophagy/physiology-
dc.subject.MESHCell Death/physiology*-
dc.subject.MESHDNA, Mitochondrial/metabolism-
dc.subject.MESHHumans-
dc.subject.MESHLongevity/physiology-
dc.subject.MESHMitochondria/physiology*-
dc.subject.MESHNecrosis-
dc.subject.MESHStress, Physiological-
dc.subject.MESHTNF-Related Apoptosis-Inducing Ligand/metabolism-
dc.titleRole of mitochondrial function in cell death and body metabolism-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine-
dc.contributor.departmentDept. of Life Science-
dc.contributor.googleauthorMyung-Shik Lee-
dc.identifier.doi10.2741/4453-
dc.contributor.localIdA02752-
dc.relation.journalcodeJ00910-
dc.identifier.eissn1093-4715-
dc.identifier.pmid27100503-
dc.identifier.urlhttps://www.bioscience.org/2016/v21/af/4453/list.htm-
dc.subject.keywordMitochondria-
dc.subject.keywordApoptosis-
dc.subject.keywordCell Death-
dc.subject.keywordROS-
dc.subject.keywordAging-
dc.subject.keywordAutophagy-
dc.subject.keywordMitokine-
dc.subject.keywordSenescence-
dc.subject.keywordReview-
dc.contributor.alternativeNameLee, Myung Shik-
dc.contributor.affiliatedAuthorLee, Myung Shik-
dc.citation.volume21-
dc.citation.startPage1233-
dc.citation.endPage1244-
dc.identifier.bibliographicCitationFRONTIERS IN BIOSCIENCE-LANDMARK, Vol.21 : 1233-1244, 2016-
dc.date.modified2017-10-24-
dc.identifier.rimsid46309-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers

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