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Control of adult neurogenesis by programmed cell death in the mammalian brain

Control of adult neurogenesis by programmed cell death in the mammalian brain
Ryu, Jae RyunHong, Caroline JeeyeonKim, Joo YeonKim, Eun-KyoungSun, WoongYu, Seong-Woon
DGIST Authors
Kim, Eun-KyoungYu, Seong-Woon
Issued Date
Article Type
Adult NeurogenesisAgingApoptosisAutophagyBrain InjuryBrain IschemiaCell IsolationCell MigrationCell ProliferationCell RenewalEnergy MetabolismFas AntigenHippocampusHumanIntracellular SignalingNecrosisNeocortexNerve Cell DifferentiationNerve Cell NecrosisNerve Cell NetworkNeural Stem CellNeural Stem CellsNeuroblastNeuroblastsNon-HumanOlfactory BulbPriority JournalProgrammed Cell DeathRetina Ganglion CellReviewScatter FactorStem Cell TransplantationSubventricular ZoneTumor Necrosis Factor-AlphaTumor Necrosis Factor Related Apoptosis Inducing Ligand
The presence of neural stem cells (NSCs) and the production of new neurons in the adult brain have received great attention from scientists and the public because of implications to brain plasticity and their potential use for treating currently incurable brain diseases. Adult neurogenesis is controlled at multiple levels, including proliferation, differentiation, migration, and programmed cell death (PCD). Among these, PCD is the last and most prominent process for regulating the final number of mature neurons integrated into neural circuits. PCD can be classified into apoptosis, necrosis, and autophagic cell death and emerging evidence suggests that all three may be important modes of cell death in neural stem/progenitor cells. However, the molecular mechanisms that regulate PCD and thereby impact the intricate balance between self-renewal, proliferation, and differentiation during adult neurogenesis are not well understood. In this comprehensive review, we focus on the extent, mechanism, and biological significance of PCD for the control of adult neurogenesis in the mammalian brain. The role of intrinsic and extrinsic factors in the regulation of PCD at the molecular and systems levels is also discussed. Adult neurogenesis is a dynamic process, and the signals for differentiation, proliferation, and death of neural progenitor/stem cells are closely interrelated. A better understanding of how adult neurogenesis is influenced by PCD will help lead to important insights relevant to brain health and diseases. © 2016 Ryu et al.
BioMed Central Ltd.
Related Researcher
  • 김은경 Kim, Eun-Kyoung 뇌과학과
  • Research Interests Neural functions in metabolic diseases; 뇌신경세포와 비만; 당뇨 등의 대사 질환 관련 연구
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Appears in Collections:
Department of Brain Sciences Lab of Neuro-Metabolism & Neurometabolomic Research Center 1. Journal Articles
Department of Brain Sciences Laboratory of Neuronal Cell Death 1. Journal Articles


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