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
  • [1] The GDNF family: Signalling, biological functions and therapeutic value
    Airaksinen, MS
    Saarma, M
    [J]. NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) : 383 - 394
  • [2] GDNF prevents degeneration and promotes the phenotype of brain noradrenergic neurons in vivo
    Arenas, E
    Trupp, M
    Akerud, P
    Ibanez, CF
    [J]. NEURON, 1995, 15 (06) : 1465 - 1473
  • [3] Stroke induces widespread changes of gene expression for glial cell line-derived neurotrophic factor family receptors in the adult rat brain
    Arvidsson, A
    Kokaia, Z
    Airaksinen, MS
    Saarma, M
    Lindvall, O
    [J]. NEUROSCIENCE, 2001, 106 (01) : 27 - 41
  • [4] GDNF family receptor complexes are emerging drug targets
    Bespalov, Maxim M.
    Saarma, Mart
    [J]. TRENDS IN PHARMACOLOGICAL SCIENCES, 2007, 28 (02) : 68 - 74
  • [5] BDNF and epilepsy: too much of a good thing?
    Binder, DK
    Croll, SD
    Gall, CM
    Scharfman, HE
    [J]. TRENDS IN NEUROSCIENCES, 2001, 24 (01) : 47 - 53
  • [6] Burke RE, 2003, ANN NY ACAD SCI, V991, P69
  • [7] D Kuipers S, 2006, CURR OPIN DRUG DISC, V9, P580
  • [8] INCREASED LEVELS OF MESSENGER-RNAS FOR NEUROTROPHIC FACTORS IN THE BRAIN DURING KINDLING EPILEPTOGENESIS
    ERNFORS, P
    BENGZON, J
    KOKAIA, Z
    PERSSON, H
    LINVALL, O
    [J]. NEURON, 1991, 7 (01) : 165 - 176
  • [9] Functional recovery in parkinsonian monkeys treated with GDNF
    Gash, DM
    Zhang, ZM
    Ovadia, A
    Cass, WA
    Yi, A
    Simmerman, L
    Russell, D
    Martin, D
    Lapchak, PA
    Collins, F
    Hoffer, BJ
    Gerhardt, GA
    [J]. NATURE, 1996, 380 (6571) : 252 - 255
  • [10] Direct brain infusion of glial cell line-derived neurotrophic factor in Parkinson disease
    Gill, SS
    Patel, NK
    Hotton, GR
    O'Sullivan, K
    McCarter, R
    Bunnage, M
    Brooks, DJ
    Svendsen, CN
    Heywood, P
    [J]. NATURE MEDICINE, 2003, 9 (05) : 589 - 595