Metabolic circuits in neural stem cells

被引:45
作者
Kim, Do-Yeon [1 ]
Rhee, Inmoo [1 ,2 ]
Paik, Jihye [1 ]
机构
[1] Weill Cornell Med Coll, Dept Pathol & Lab Med, New York, NY 10065 USA
[2] Gachon Univ, Sch Med, Dept Biochem, Incheon 406799, South Korea
关键词
Neural stem/progenitor cells; Metabolism; Self-renewal; Differentiation; ADULT SUBVENTRICULAR ZONE; TUMOR-SUPPRESSOR P53; GROWTH-FACTOR-I; GLUTAMINE-METABOLISM; SELF-RENEWAL; C-MYC; HIPPOCAMPAL NEUROGENESIS; AEROBIC GLYCOLYSIS; ENERGY-METABOLISM; OXIDATIVE STRESS;
D O I
10.1007/s00018-014-1686-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic activity indicative of cellular demand is emerging as a key player in cell fate decision. Numerous studies have demonstrated that diverse metabolic pathways have a critical role in the control of the proliferation, differentiation and quiescence of stem cells. The identification of neural stem/progenitor cells (NSPCs) and the characterization of their development and fate decision process have provided insight into the regenerative potential of the adult brain. As a result, the potential of NSPCs in cell replacement therapies for neurological diseases is rapidly growing. The aim of this review is to discuss the recent findings on the crosstalk among key regulators of NSPC development and the metabolic regulation crucial for the function and cell fate decisions of NSPCs. Fundamental understanding of the metabolic circuits in NSPCs may help to provide novel approaches for reactivating neurogenesis to treat degenerative brain conditions and cognitive decline.
引用
收藏
页码:4221 / 4241
页数:21
相关论文
共 214 条
  • [1] Åberg MAI, 2000, J NEUROSCI, V20, P2896
  • [2] Multilineage embryonic hematopoiesis requires hypoxic ARNT activity
    Adelman, DM
    Maltepe, E
    Simon, MC
    [J]. GENES & DEVELOPMENT, 1999, 13 (19) : 2478 - 2483
  • [3] Metabolic differentiation in the embryonic retina
    Agathocleous, Michalis
    Love, Nicola K.
    Randlett, Owen
    Harris, Julia J.
    Liu, Jinyue
    Murray, Andrew J.
    Harris, William A.
    [J]. NATURE CELL BIOLOGY, 2012, 14 (08) : 859 - U180
  • [4] POSTNATAL NEUROGENESIS IN GUINEA-PIG
    ALTMAN, J
    DAS, GD
    [J]. NATURE, 1967, 214 (5093) : 1098 - &
  • [5] AUTORADIOGRAPHIC INVESTIGATION OF CELL PROLIFERATION IN BRAINS OF RATS AND CATS
    ALTMAN, J
    [J]. ANATOMICAL RECORD, 1963, 145 (04): : 573 - &
  • [6] ARE NEW NEURONS FORMED IN BRAINS OF ADULT MAMMALS
    ALTMAN, J
    [J]. SCIENCE, 1962, 135 (3509) : 1127 - &
  • [7] Cognitive dysfunction and hippocampal changes in experimental type 1 diabetes
    Alvarez, Edgardo O.
    Beauquis, Juan
    Revsin, Yanina
    Banzan, Arturo M.
    Roig, Paulina
    De Nicola, Alejandro F.
    Saravia, Flavia
    [J]. BEHAVIOURAL BRAIN RESEARCH, 2009, 198 (01) : 224 - 230
  • [8] Inhibition of Pyruvate Kinase M2 by Reactive Oxygen Species Contributes to Cellular Antioxidant Responses
    Anastasiou, Dimitrios
    Poulogiannis, George
    Asara, John M.
    Boxer, Matthew B.
    Jiang, Jian-kang
    Shen, Min
    Bellinger, Gary
    Sasaki, Atsuo T.
    Locasale, Jason W.
    Auld, Douglas S.
    Thomas, Craig J.
    Vander Heiden, Matthew G.
    Cantley, Lewis C.
    [J]. SCIENCE, 2011, 334 (6060) : 1278 - 1283
  • [9] Therapeutic value of prenatal rapamycin treatment in a mouse brain model of tuberous sclerosis complex
    Anderl, Stefanie
    Freeland, Megan
    Kwiatkowski, David J.
    Goto, June
    [J]. HUMAN MOLECULAR GENETICS, 2011, 20 (23) : 4597 - 4604
  • [10] Androutsellis-Theotokis A, 2006, NATURE, V442, P823, DOI 10.1038/nature04940