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dc.contributor.author Yeo, Bo Kyoung -
dc.contributor.author Hong, Caroline Jeeyeon -
dc.contributor.author Chung, Kyung Min -
dc.contributor.author Woo, Hanwoong -
dc.contributor.author Kim, Kyungchan -
dc.contributor.author Jung, Seonghee -
dc.contributor.author Kim, Eun-Kyoung -
dc.contributor.author Yu, Seong-Woon -
dc.date.available 2017-07-05T08:45:54Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016-03 -
dc.identifier.issn 1756-6606 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2289 -
dc.description.abstract Background: Programmed cell death (PCD) plays essential roles in the regulation of survival and function of neural stem cells (NSCs). Abnormal regulation of this process is associated with developmental and degenerative neuronal disorders. However, the mechanisms underlying the PCD of NSCs remain largely unknown. Understanding the mechanisms of PCD in NSCs is crucial for exploring therapeutic strategies for the treatment of neurodegenerative diseases. Result: We have previously reported that adult rat hippocampal neural stem (HCN) cells undergo autophagic cell death (ACD) following insulin withdrawal without apoptotic signs despite their normal apoptotic capabilities. It is unknown how interconnection between ACD and apoptosis is mediated in HCN cells. Valosin-containing protein (VCP) is known to be essential for autophagosome maturation in mammalian cells. VCP is abundantly expressed in HCN cells compared to hippocampal tissue and neurons. Pharmacological and genetic inhibition of VCP at basal state in the presence of insulin modestly impaired autophagic flux, consistent with its known role in autophagosome maturation. Of note, VCP inaction in insulin-deprived HCN cells significantly decreased ACD and down-regulated autophagy initiation signals with robust induction of apoptosis. Overall autophagy level was also substantially reduced, suggesting the novel roles of VCP at initial step of autophagy. Conclusion: Taken together, these data demonstrate that VCP may play an essential role in the initiation of autophagy and mediation of crosstalk between ACD and apoptosis in HCN cells when autophagy level is high upon insulin withdrawal. This is the first report on the role of VCP in regulation of NSC cell death. Elucidating the mechanism by which VCP regulates the crosstalk of ACD and apoptosis will contribute to understanding the molecular mechanism of PCD in NSCs. © 2016 Yeo et al. -
dc.language English -
dc.publisher BioMed Central Ltd. -
dc.title Valosin-containing protein is a key mediator between autophagic cell death and apoptosis in adult hippocampal neural stem cells following insulin withdrawal -
dc.type Article -
dc.identifier.doi 10.1186/s13041-016-0212-8 -
dc.identifier.scopusid 2-s2.0-84964354813 -
dc.identifier.bibliographicCitation Molecular Brain, v.9, no.1 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordAuthor Autophagic cell death -
dc.subject.keywordAuthor Apoptosis -
dc.subject.keywordAuthor Adult neural stem cells -
dc.subject.keywordAuthor Insulin withdrawal -
dc.subject.keywordAuthor Valosin-containing protein -
dc.subject.keywordPlus AAA-ATPASE -
dc.subject.keywordPlus Adult -
dc.subject.keywordPlus Adult Neural Stem Cells -
dc.subject.keywordPlus Animal Cell -
dc.subject.keywordPlus Animal Tissue -
dc.subject.keywordPlus APOPTOSIS -
dc.subject.keywordPlus Article -
dc.subject.keywordPlus Autophagic Cell Death -
dc.subject.keywordPlus Autophagosome -
dc.subject.keywordPlus Autophagy -
dc.subject.keywordPlus Brain Nerve Cell -
dc.subject.keywordPlus Controlled Study -
dc.subject.keywordPlus DEGRADATION -
dc.subject.keywordPlus DISEASE -
dc.subject.keywordPlus Down Regulation -
dc.subject.keywordPlus Drug Withdrawal -
dc.subject.keywordPlus embryo -
dc.subject.keywordPlus ENDOPLASMIC-RETICULUM STRESS -
dc.subject.keywordPlus Gene Inactivation -
dc.subject.keywordPlus Hippocampus -
dc.subject.keywordPlus IDENTIFICATION -
dc.subject.keywordPlus Insulin -
dc.subject.keywordPlus Insulin Withdrawal -
dc.subject.keywordPlus Membrane Transport -
dc.subject.keywordPlus Neural Stem Cell -
dc.subject.keywordPlus Nonhuman -
dc.subject.keywordPlus P97 -
dc.subject.keywordPlus PATHWAYS -
dc.subject.keywordPlus Priority Journal -
dc.subject.keywordPlus Protein Degradation -
dc.subject.keywordPlus Protein Expression -
dc.subject.keywordPlus Protein Transport -
dc.subject.keywordPlus Rat -
dc.subject.keywordPlus Regulatory Mechanism -
dc.subject.keywordPlus Signal Transduction -
dc.subject.keywordPlus Ubiquitin -
dc.subject.keywordPlus Valosin-Containing Protein -
dc.subject.keywordPlus VCP -
dc.subject.keywordPlus VCP/P97 -
dc.citation.number 1 -
dc.citation.title Molecular Brain -
dc.citation.volume 9 -

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