MANF is widely expressed in mammalian tissues and differently regulated after ischemic and epileptic insults in rodent brain

被引:171
作者
Lindholm, Paivi [1 ]
Peranen, Johan [1 ]
Andressoo, Jaan-Olle [1 ]
Kalkkinen, Nisse [1 ]
Kokaia, Zaal [2 ]
Lindvall, Olle [2 ]
Timmusk, Tonis [1 ,3 ]
Saarma, Mart
机构
[1] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
[2] Univ Lund Hosp, Lund Strateg Res Ctr Stem Cell Biol & Cell Therap, SE-22184 Lund, Sweden
[3] Tallinn Univ Technol, Dept Gene Technol, EE-19086 Tallinn, Estonia
基金
瑞典研究理事会; 芬兰科学院;
关键词
MANF; ARMET; CDNF; Dopaminergic; Expression; Immunohistochemistry; Ischemia; Status epilepticus;
D O I
10.1016/j.mcn.2008.07.016
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The mesencephalic astrocyte-derived neurotrophic factor (MANF) has been described as a Survival factor for dopaminergic neurons in vitro, but its expression in mammalian tissues is poorly known. MANF and a homologous Protein, the conserved dopamine neurotrophic factor (CDNF), form a novel evolutionary conserved family of neurotrophic factors. Here we used in situ hybridization and immunohistochemistry to characterize MANF expression in developing and adult mouse. MANF expression was widespread in the nervous system and non-neuronal tissues. In the brain, relatively high MANF levels were detected in the cerebral cortex, hippocampus and cerebellar Purkinje cells. After status epilepticus, Manf mRNA expression was transiently increased in the dentate granule cell layer of hippocampus, thalamic reticular nucleus and in several cortical areas. In contrast, following global forebrain ischemia changes in Manf expression were widespread in the hippocampal formation and more restricted in cerebral cortex. The widespread expression of MANF together with its evolutionary conserved nature and regulation by brain insults suggest that it has important functions both under normal and pathological conditions in many tissue types. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:356 / 371
页数:16
相关论文
共 44 条
  • [11] Chronic, controlled GDNF infusion promotes structural and functional recovery in advanced parkinsonian monkeys
    Grondin, R
    Zhang, ZM
    Yi, A
    Cass, WA
    Maswood, N
    Andersen, AH
    Elsberry, DD
    Klein, MC
    Gerhardt, GA
    Gash, DM
    [J]. BRAIN, 2002, 125 : 2191 - 2201
  • [12] Intraventricular infusion of TrkB-Fc fusion protein promotes ischemia-induced neurogenesis in adult rat dentate gyrus
    Gustafsson, E
    Lindvall, O
    Kokaia, Z
    [J]. STROKE, 2003, 34 (11) : 2710 - 2715
  • [13] GLIAL-CELL LINE-DERIVED NEUROTROPHIC FACTOR REVERSES TOXIN-INDUCED INJURY TO MIDBRAIN DOPAMINERGIC-NEURONS IN-VIVO
    HOFFER, BJ
    HOFFMAN, A
    BOWENKAMP, K
    HUETTL, P
    HUDSON, J
    MARTIN, D
    LIN, LFH
    GERHARDT, GA
    [J]. NEUROSCIENCE LETTERS, 1994, 182 (01) : 107 - 111
  • [14] Neurotrophins: Roles in neuronal development and function
    Huang, EJ
    Reichardt, LF
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 : 677 - 736
  • [15] Environment matters: Synaptic properties of neurons born in the epileptic adult brain develop to reduce excitability
    Jakubs, Katherine
    Nanobashvili, Avtandil
    Bonde, Sara
    Ekdahl, Christine T.
    Kokaia, Zaal
    Kokaia, Merab
    Lindvall, Olle
    [J]. NEURON, 2006, 52 (06) : 1047 - 1059
  • [16] Protection against ischemic brain damage by GDNF affecting cell survival and death signals
    Jin, G
    Omori, N
    Li, F
    Nagano, I
    Manabe, Y
    Shoji, M
    Abe, K
    [J]. NEUROLOGICAL RESEARCH, 2003, 25 (03) : 249 - 253
  • [17] GDNF PROTECTS NIGRAL DOPAMINE NEURONS AGAINST 6-HYDROXYDOPAMINE IN-VIVO
    KEARNS, CM
    GASH, DM
    [J]. BRAIN RESEARCH, 1995, 672 (1-2) : 104 - 111
  • [18] Neurogenesis after ischaemic brain insults
    Kokaia, Z
    Lindvall, O
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 2003, 13 (01) : 127 - 132
  • [19] GDNF family ligands and receptors are differentially regulated after brain insults in the rat
    Kokaia, Z
    Airaksinen, MS
    Nanobashvili, A
    Larsson, E
    Kujamäki, E
    Lindvall, O
    Saarma, M
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (04) : 1202 - 1216
  • [20] Absence of ret signaling in mice causes progressive and late degeneration of the nigrostriatal system
    Kramer, Edgar R.
    Aron, Liviu
    Ramakers, Geert M. J.
    Seitz, Sabine
    Zhuang, Xiaoxi
    Beyer, Klaus
    Smidt, Marten P.
    Klein, Ruediger
    [J]. PLOS BIOLOGY, 2007, 5 (03) : 616 - 628