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Autophagy for the quality control of adult hippocampal neural stem cells
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dc.contributor.author Hong, Caroline Jeeyeon -
dc.contributor.author Park, Hyunhee -
dc.contributor.author Yu, Seong-Woon -
dc.date.available 2017-07-05T08:32:10Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016-10-15 -
dc.identifier.issn 0006-8993 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2174 -
dc.description.abstract Autophagy plays an important role in neurodegeneration, as well as in normal brain development and function. Recent studies have also implicated autophagy in the regulation of stemness and neurogenesis in neural stem cells (NSCs). However, little is known regarding the roles of autophagy in NSC biology. It has been shown that in addition to cytoprotective roles of autophagy, pro-death autophagy, or ׳autophagic cell death (ACD),’ regulates the quantity of adult NSCs. A tight regulation of survival and death of NSCs residing in the neurogenic niches through programmed cell death (PCD) is critical for maintenance of adult neurogenesis. ACD plays a primary role in the death of adult hippocampal neural stem (HCN) cells following insulin withdrawal. Despite the normal apoptotic capability of HCN cells, they are committed to death by autophagy following insulin withdrawal, suggesting the existence of a unique regulatory program that controls the mode of cell death. We propose that dual roles of autophagy for maintenance of NSC pluripotency, as well as for elimination of defective NSCs, may serve as a combined NSC quality control mechanism. This article is part of a Special Issue entitled SI:Autophagy. © 2016 Elsevier B.V. -
dc.publisher ELSEVIER SCIENCE BV -
dc.title Autophagy for the quality control of adult hippocampal neural stem cells -
dc.type Article -
dc.identifier.doi 10.1016/j.brainres.2016.02.048 -
dc.identifier.scopusid 2-s2.0-84961231052 -
dc.identifier.bibliographicCitation Hong, Caroline Jeeyeon. (2016-10-15). Autophagy for the quality control of adult hippocampal neural stem cells. Brain Research, 1649, 166–172. doi: 10.1016/j.brainres.2016.02.048 -
dc.subject.keywordAuthor Hippocampal neural stem cell -
dc.subject.keywordAuthor Programmed cell death -
dc.subject.keywordAuthor Autophagic cell death -
dc.subject.keywordAuthor GSK-3 beta -
dc.subject.keywordAuthor Calpain -
dc.subject.keywordAuthor Apoptosis -
dc.subject.keywordPlus APOPTOSIS -
dc.subject.keywordPlus Autophagic Cell Death -
dc.subject.keywordPlus BAX ACTIVATION -
dc.subject.keywordPlus Calpain -
dc.subject.keywordPlus DEATH -
dc.subject.keywordPlus DISTINCT ACTIONS -
dc.subject.keywordPlus GLYCOGEN-SYNTHASE KINASE-3-BETA -
dc.subject.keywordPlus GROWTH-FACTOR-I -
dc.subject.keywordPlus GSK-3 Beta -
dc.subject.keywordPlus Hippocampal Neural stem Cell -
dc.subject.keywordPlus Insulin Withdrawal -
dc.subject.keywordPlus NERVOUS-system -
dc.subject.keywordPlus NEURONAL DEGENERATION -
dc.subject.keywordPlus Programmed Cell Death -
dc.subject.keywordPlus PROGRAMMED NECROSIS -
dc.citation.endPage 172 -
dc.citation.startPage 166 -
dc.citation.title Brain Research -
dc.citation.volume 1649 -
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