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dc.contributor.author Park, Hyun Ha -
dc.contributor.author Kim, Byeong-Hyeon -
dc.contributor.author Leem, Seol Hwa -
dc.contributor.author Park, Yong Ho -
dc.contributor.author Hoe, Hyang-Sook -
dc.contributor.author Nam, Yunkwon -
dc.contributor.author Kim, Sujin -
dc.contributor.author Shin, Soo Jung -
dc.contributor.author Moon, Minho -
dc.date.accessioned 2024-02-15T14:40:15Z -
dc.date.available 2024-02-15T14:40:15Z -
dc.date.created 2023-10-25 -
dc.date.issued 2023-09 -
dc.identifier.issn 1976-6696 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/47950 -
dc.description.abstract Alzheimer’s disease (AD) is a progressive neurodegenerative disease characterized by cognitive decline. Several recent studies demonstrated that impaired adult neurogenesis could contribute to AD-related cognitive impairment. Adult subventricular zone (SVZ) neurogenesis, which occurs in the lateral ventricles, plays a crucial role in structural plasticity and neural circuit maintenance. Alterations in adult SVZ neurogenesis are early events in AD, and impaired adult neurogenesis is influenced by the accumulation of intracellular Aβ. Although Aβ-overexpressing transgenic 5XFAD mice are an AD animal model well representative of Aβ-related pathologies in the brain, the characterization of altered adult SVZ neurogenesis following AD progression in 5XFAD mice has not been thoroughly examined. Therefore, we validated the characterization of adult SVZ neurogenesis changes with AD progression in 2-, 4-, 8-, and 11-monthold male 5XFAD mice. We first investigated the Aβ accumulation in the SVZ using the 4G8 antibody. We observed intracellular Aβ accumulation in the SVZ of 2-month-old 5XFAD mice. In addition, 5XFAD mice exhibited significantly increased Aβ deposition in the SVZ with age. Next, we performed a histological analysis to investigate changes in various phases of adult neurogenesis, such as quiescence, proliferation, and differentiation, in SVZ. Compared to age-matched wild-type (WT) mice, quiescent neural stem cells were reduced in 5XFAD mice from 2-11 months of age. Moreover, proliferative neural stem cells were decreased in 5XFAD mice from 2 to 8 months of age. Furthermore, differentiations of neuroblasts were diminished in 5XFAD mice from 2-11 months of age. Intriguingly, we found that adult SVZ neurogenesis was reduced with aging in healthy mice. Taken together, our results revealed that impairment of adult SVZ neurogenesis appears with aging or AD progression. © 2023 by the The Korean Society for Biochemistry and Molecular Biology -
dc.language English -
dc.publisher The Biochemical Society of the Republic of Korea -
dc.title Characterization of age- and stage-dependent impaired adult subventricular neurogenesis in 5XFAD mouse model of Alzheimer’s disease -
dc.type Article -
dc.identifier.doi 10.5483/BMBRep.2023-0071 -
dc.identifier.wosid 001079798500008 -
dc.identifier.scopusid 2-s2.0-85173038195 -
dc.identifier.bibliographicCitation BMB Reports, v.56, no.9, pp.520 - 525 -
dc.identifier.kciid ART002998790 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordAuthor 5XFAD mice -
dc.subject.keywordAuthor Adult neurogenesis -
dc.subject.keywordAuthor Alzheimer&apos -
dc.subject.keywordAuthor s disease -
dc.subject.keywordAuthor Amyloid beta -
dc.subject.keywordAuthor Subventricular zone -
dc.subject.keywordPlus NEURAL STEM-CELLS -
dc.subject.keywordPlus HIPPOCAMPAL NEUROGENESIS -
dc.subject.keywordPlus AMYLOID-BETA -
dc.subject.keywordPlus SVZ CELLS -
dc.subject.keywordPlus NEURONS -
dc.subject.keywordPlus ACCUMULATION -
dc.subject.keywordPlus ZONE -
dc.subject.keywordPlus MICE -
dc.citation.endPage 525 -
dc.citation.number 9 -
dc.citation.startPage 520 -
dc.citation.title BMB Reports -
dc.citation.volume 56 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.relation.journalResearchArea Biochemistry & Molecular Biology -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology -
dc.type.docType Article -
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