Roles of Nitric Oxide Synthase Isoforms in Neurogenesis

被引:37
作者
Chong, Cheong-Meng [1 ]
Ai, Nana [2 ]
Ke, Minjing [1 ]
Tan, Yuan [1 ]
Huang, Zhijian [1 ]
Li, Yong [3 ]
Lu, Jia-Hong [1 ]
Ge, Wei [2 ]
Su, Huanxing [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau, Peoples R China
[2] Univ Macau, Fac Hlth Sci, Macau, Peoples R China
[3] Shanghai Jiao Tong Univ, Inst Med Sci, Dept Biochem & Mol Cell Biol, Sch Med, Shanghai 200025, Peoples R China
关键词
Nitric oxide; Nitric oxide synthase; Neural stem cells; Proliferation; Neurogenesis; NEURAL STEM-CELLS; GROWTH-FACTOR RECEPTOR; CENTRAL-NERVOUS-SYSTEM; SUBVENTRICULAR ZONE; ADULT NEUROGENESIS; DENTATE GYRUS; IN-VITRO; BRAIN; PROLIFERATION; DIFFERENTIATION;
D O I
10.1007/s12035-017-0513-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nitric oxide (NO), a free radical gas, acts as a neurotransmitter or neuromodulator in the central nervous system (CNS). It has been widely explored as a mediator of neuroinflammation, neuronal damages, and neurodegeneration at its pathological levels. Recently, increasing evidence suggests that NO plays key roles in mediating adult neurogenesis, the process of neural stem cells (NSCs) to generate newborn neurons for replacing damaged neurons or maintaining the function of the brain. NO synthase (NOS) is a major enzyme catalyzing the generation of NO in the brain. Recent studies indicate that three homologous NOS isoforms are involved in the proliferation of NSCs and neurogenesis. Therefore, the impact of NOS isoforms on NSC functions needs to be elucidated. Here, we summarize the studies on the role of NO and NOS with different isoforms in NSC proliferation and neurogenesis with the focus on introducing action mechanisms involved in the regulation of NSC function. This growing research area provides the new insight into controlling NSC function via regulating NO microenvironment in the brain. It also provides the evidence on targeting NOS for the treatment of brain diseases.
引用
收藏
页码:2645 / 2652
页数:8
相关论文
共 65 条
  • [1] Nitric oxide synthases: structure, function and inhibition
    Alderton, WK
    Cooper, CE
    Knowles, RG
    [J]. BIOCHEMICAL JOURNAL, 2001, 357 (03) : 593 - 615
  • [2] Neuronal replacement from endogenous precursors in the adult brain after stroke
    Arvidsson, A
    Collin, T
    Kirik, D
    Kokaia, Z
    Lindvall, O
    [J]. NATURE MEDICINE, 2002, 8 (09) : 963 - 970
  • [3] Bauer S, 2003, J NEUROSCI, V23, P1792
  • [4] Nitric oxide regulates astrocyte maturation in the hippocampus: Involvement of NOS2
    Bechade, Catherine
    Pascual, Olivier
    Triller, Antoine
    Bessis, Alain
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 2011, 46 (04) : 762 - 769
  • [5] Bon CLM, 2003, J NEUROSCI, V23, P1941
  • [6] Endogenous nitric oxide synthesis: Biological functions and pathophysiology
    Bredt, DS
    [J]. FREE RADICAL RESEARCH, 1999, 31 (06) : 577 - 596
  • [7] Nitric oxide and neuronal death
    Brown, Guy C.
    [J]. NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 2010, 23 (03): : 153 - 165
  • [8] Nitric oxide in the central nervous system: neuroprotection versus neurotoxicity
    Calabrese, Vittorio
    Mancuso, Cesare
    Calvani, Menotti
    Rizzarelli, Enrico
    Butterfield, D. Allan
    Stella, Anna Maria Giuffrida
    [J]. NATURE REVIEWS NEUROSCIENCE, 2007, 8 (10) : 766 - 775
  • [9] Telomerase activity in the subventricular zone of adult mice
    Caporaso, GL
    Lim, DA
    Alvarez-Buylla, A
    Chao, MV
    [J]. MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 23 (04) : 693 - 702
  • [10] Nitric oxide from inflammatory origin impairs neural stem cell proliferation by inhibiting epidermal growth factor receptor signaling
    Carreira, Bruno P.
    Morte, Maria I.
    Santos, Ana I.
    Lourenco, Ana S.
    Ambrosio, Antonio F.
    Carvalho, Caetana M.
    Araujo, Ines M.
    [J]. FRONTIERS IN CELLULAR NEUROSCIENCE, 2014, 8