Profiling of cytosolic and mitochondrial H2O2 production using the H2O2-sensitive protein HyPer in LPS-induced microglia cells

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dc.contributor.authorJunghyung Park-
dc.contributor.authorS Lee-
dc.contributor.authorH S Lee-
dc.contributor.authorSang-Rae Lee-
dc.contributor.authorD S Lee-
dc.date.accessioned2017-08-29-
dc.date.available2017-08-29-
dc.date.issued2017-
dc.identifier.issn0304-3940-
dc.identifier.uri10.1016/j.neulet.2017.06.017ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/17243-
dc.description.abstractDysregulation of the production of pro-inflammatory mediators in microglia exacerbates the pathologic process of neurodegenerative disease. ROS actively affect microglia activation by regulating transcription factors that control the expression of pro-inflammatory genes. However, accurate information regarding the function of ROS in different subcellular organelles has not yet been established. Here, we analyzed the pattern of cytosolic and mitochondrial H2O2 formation in LPS-activated BV-2 microglia using the H2O2-sensitive protein HyPer targeted to specific subcellular compartments. Our results show that from an early time, cytosolic H2O2 started increasing constantly, whereas mitochondrial H2O2 rapidly increased later. In addition, we found that MAPK affected cytosolic H2O2, but not mitochondrial H2O2. Consequently, our study provides the basic information about subcellular H2O2 generation in activated microglia, and a useful tool for investigating molecular targets that can modulate neuroinflammatory responses.-
dc.publisherElsevier-
dc.titleProfiling of cytosolic and mitochondrial H2O2 production using the H2O2-sensitive protein HyPer in LPS-induced microglia cells-
dc.title.alternativeProfiling of cytosolic and mitochondrial H2O2 production using the H2O2-sensitive protein HyPer in LPS-induced microglia cells-
dc.typeArticle-
dc.citation.titleNeuroscience Letters-
dc.citation.number0-
dc.citation.endPage11-
dc.citation.startPage6-
dc.citation.volume654-
dc.contributor.affiliatedAuthorJunghyung Park-
dc.contributor.affiliatedAuthorSang-Rae Lee-
dc.contributor.alternativeName박정형-
dc.contributor.alternativeName이승훈-
dc.contributor.alternativeName이현식-
dc.contributor.alternativeName이상래-
dc.contributor.alternativeName이동석-
dc.identifier.bibliographicCitationNeuroscience Letters, vol. 654, pp. 6-11-
dc.identifier.doi10.1016/j.neulet.2017.06.017-
dc.subject.keywordHydrogen peroxide-
dc.subject.keywordHyPer-
dc.subject.keywordLipopolysaccharide-
dc.subject.keywordMicroglia-
dc.subject.keywordMitogen-activated protein kinase-
dc.subject.keywordReactive oxygen species-
dc.subject.localHydrogen peroxide-
dc.subject.localhydrogen peroxide-
dc.subject.localHyPer-
dc.subject.localHyper-
dc.subject.localLipopolysaccharide-
dc.subject.localLipopolysaccharide (LPS)-
dc.subject.localLipopolysaccharides-
dc.subject.locallipopolysaccharide-
dc.subject.locallipopolysaccharide (LPS)-
dc.subject.localmicroglia-
dc.subject.localMicroglia-
dc.subject.localmitogen activated protein kinase-
dc.subject.localmitogen-activated protein kinase-
dc.subject.localmitogen-activated protein kinases-
dc.subject.localMitogen activated protein kinase-
dc.subject.localMitogen-acti-vated protein kinase-
dc.subject.localMitogen-activated protein kinase-
dc.subject.localMitogen-activated protein kinase (MAPK)-
dc.subject.localMitogen-activated protein kinases-
dc.subject.localMitogen-activated protein kinases (MAPKs)-
dc.subject.localMitogen-activated protein (MAP) kinase-
dc.subject.localMitogenactivated protein kinase-
dc.subject.localROS-
dc.subject.localReactive Oxygen Species (ROS)-
dc.subject.localReactive oxidative species-
dc.subject.localReactive oxygen species-
dc.subject.localReactive oxygen species (ROS)-
dc.subject.localreactive oxygen species-
dc.subject.localreactive oxygen species (ROS)-
dc.subject.localReactive Oxygen Species-
dc.subject.localReactive oxygen species(ROS)-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > National Primate Research Center > 1. Journal Articles
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