Identification of a novel gene, OASIS, which encodes for a putative CREB ATF family transcription factor in the long-term cultured astrocytes and gliotic tissue

被引:95
作者
Honma, Y
Kanazawa, K
Mori, T
Tanno, Y
Tojo, M
Kiyosawa, H
Takeda, J
Nikaido, T
Tsukamoto, T
Yokoya, S
Wanaka, A
机构
[1] Inst Biomed Sci, Dept Cell Sci, Fukushima 9601295, Japan
[2] Fukushima Med Univ, Dept Neurol, Sch Med, Fukushima 9601295, Japan
[3] Iwaki Kyoritsu Hosp, Dept Neurol, Iwaki, Fukushima, Japan
来源
MOLECULAR BRAIN RESEARCH | 1999年 / 69卷 / 01期
关键词
gliosis; molecular cloning; CREB ATF; in situ hybridization; reactive astrocyte;
D O I
10.1016/S0169-328X(99)00102-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Gliosis is a characteristic response of astrocytes to inflammation and trauma of the central nervous system (CNS), To study the mechanisms underlying gliosis, we performed differential display screening for genes specifically induced in long-term cultured astrocytes used as an in vitro gliosis model. We identified and characterized a gene (named OASIS, for old astrocyte specifically-induced substance) expressed in long-term cultured mouse astrocytes, or 'old astrocytes (OG)'. The OASIS gene encoded a putative transcription factor belonging to the cyclic AMP responsive element binding protein/activating transcription factor (CREB/ATF) gene family, with homology to box B-binding factor-2 (BBF-2), a Drosophila transcription factor. Its expression was developmentally regulated; OASIS mRNA was primarily expressed in the salivary gland and cartilage in the mouse embryo and it was transiently upregulated in the brain during postnatal two weeks. The expression became weaker in the adult brain. We also demonstrated that an expression of the OASIS mRNA was induced in response to the cryo-injury of the mouse cerebral cortex, The distribution pattern of the OASIS-positive cells in the injured cortex was very similar to that of the glial fibrillary acidic protein (GFAP)-positive cells. These results suggest that OASIS protein may play a role in gliotic events. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:93 / 103
页数:11
相关论文
共 30 条
  • [1] A DROSOPHILA CREB ATF TRANSCRIPTIONAL ACTIVATOR BINDS TO BOTH FAT BODY-SPECIFIC AND LIVER-SPECIFIC REGULATORY ELEMENTS
    ABEL, T
    BHATT, R
    MANIATIS, T
    [J]. GENES & DEVELOPMENT, 1992, 6 (03) : 466 - 480
  • [2] Differential expression of peroxisome proliferator-activated receptors (PPARs): Tissue distribution of PPAR-alpha, -beta, and -gamma in the adult rat
    Braissant, O
    Foufelle, F
    Scotto, C
    Dauca, M
    Wahli, W
    [J]. ENDOCRINOLOGY, 1996, 137 (01) : 354 - 366
  • [3] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [4] CONDORELLI DF, 1994, J NEUROCHEM, V63, P509
  • [5] CREB: A major mediator of neuronal neurotrophin responses
    Finkbeiner, S
    Tavazoie, SF
    Maloratsky, A
    Jacobs, KM
    Harris, KM
    Greenberg, ME
    [J]. NEURON, 1997, 19 (05) : 1031 - 1047
  • [6] Fitzgerald LR, 1996, J NEUROCHEM, V66, P429
  • [7] Geisert EE, 1996, J NEUROSCI, V16, P5478
  • [8] THE TRANSCRIPTION FACTORS C-JUN, JUN D AND CREB, BUT NOT FOS AND KROX-24, ARE DIFFERENTIALLY REGULATED IN AXOTOMIZED NEURONS FOLLOWING TRANSECTION OF RAT SCIATIC-NERVE
    HERDEGEN, T
    FIALLOSESTRADA, CE
    SCHMID, W
    BRAVO, R
    ZIMMERMANN, M
    [J]. MOLECULAR BRAIN RESEARCH, 1992, 14 (03): : 155 - 165
  • [9] EXPRESSION OF P75NGFR TRKA, AND TRKB MESSENGER-RNA IN RAT-C6 GLIOMA AND TYPE-I ASTROCYTE CULTURES
    HUTTON, LA
    DEVELLIS, J
    PEREZPOLO, JR
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 1992, 32 (03) : 375 - 383
  • [10] Molecular cloning of a novel polypeptide, DP5, induced during programmed neuronal death
    Imaizumi, K
    Tsuda, M
    Imai, Y
    Wanaka, A
    Takagi, T
    Tohyama, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (30) : 18842 - 18848