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Department of Brain Sciences
Laboratory of Neuronal Cell Death
1. Journal Articles
Autophagy for the quality control of adult hippocampal neural stem cells
Hong, Caroline Jeeyeon
;
Park, Hyunhee
;
Yu, Seong-Woon
Department of Brain Sciences
Laboratory of Neuronal Cell Death
1. Journal Articles
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Title
Autophagy for the quality control of adult hippocampal neural stem cells
Issued Date
2016-10-15
Citation
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
Type
Article
Author Keywords
Hippocampal neural stem cell
;
Programmed cell death
;
Autophagic cell death
;
GSK-3 beta
;
Calpain
;
Apoptosis
Keywords
APOPTOSIS
;
Autophagic Cell Death
;
BAX ACTIVATION
;
Calpain
;
DEATH
;
DISTINCT ACTIONS
;
GLYCOGEN-SYNTHASE KINASE-3-BETA
;
GROWTH-FACTOR-I
;
GSK-3 Beta
;
Hippocampal Neural stem Cell
;
Insulin Withdrawal
;
NERVOUS-system
;
NEURONAL DEGENERATION
;
Programmed Cell Death
;
PROGRAMMED NECROSIS
ISSN
0006-8993
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.
URI
http://hdl.handle.net/20.500.11750/2174
DOI
10.1016/j.brainres.2016.02.048
Publisher
ELSEVIER SCIENCE BV
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