Nuclear factor-I regulates glial fibrillary acidic protein gene expression in astrocytes differentiated from cortical precursor cells

被引:66
作者
Cebolla, B [1 ]
Vallejo, M [1 ]
机构
[1] Univ Autonoma Madrid, CSIC, Inst Invest Biomed Alberto Sols, E-28029 Madrid, Spain
关键词
astrocyte differentiation; ciliary neurotrophic factor; neural progenitor cells; pituitary adenylate cyclase-activating polypeptide; process outgrowth; transcription factors;
D O I
10.1111/j.1471-4159.2006.03804.x
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
The elucidation of the transcriptional mechanisms that regulate glial fibrillary acidic protein (GFAP) gene expression is important for the understanding of the molecular mechanisms that control astrocyte differentiation during brain development. We investigated regulatory elements located in a proximal region of the GFAP promoter, important for expression in cortical precursor cells differentiating into astrocytes. One of these elements recognizes transcription factors of the nuclear factor-I family (NFI). We found that, in primary cultures of cortical cells, NFI occupies the GFAP promoter prior to the induction of astrocyte differentiation. In the developing cerebral cortex, the onset of expression of NFI coincides chronologically with the beginning of astrocytogenesis. Mutational analysis of the GFAP gene and transfections in primary cortical precursors show that inhibition of binding of NFI to the GFAP promoter results in decreased levels of transcriptional activity and is required for the synergistic stimulation of the GFAP promoter by the astrogenic agents, pituitary adenylate cyclase-activating polypeptide and ciliary neurotrophic factor, which in combination enhance astrocyte differentiation to generate astrocytes with longer processes. Thus, NFI appears to be an important factor for the integration of astrogenic stimuli in the developing central nervous system.
引用
收藏
页码:1057 / 1070
页数:14
相关论文
共 56 条
[1]   Radial glia serve as neuronal progenitors in all regions of the central nervous system [J].
Anthony, TE ;
Klein, C ;
Fishell, G ;
Heintz, N .
NEURON, 2004, 41 (06) :881-890
[2]  
Barnett SC, 1995, DEVELOPMENT, V121, P3969
[3]  
Bedford FK, 1998, J NEUROSCI, V18, P6186
[4]   Nuclear factor 1 and octamer transcription factor 1 binding preset the chromatin structure of the mouse mammary tumor virus promoter for hormone induction [J].
Belikov, S ;
Holmqvist, PH ;
Åstrand, C ;
Wrange, Ö .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :49857-49867
[5]   Regulation of gliogenesis in the central nervous system by the JAK-STAT signaling pathway [J].
Bonni, A ;
Sun, Y ;
NadalVicens, M ;
Bhatt, A ;
Frank, DA ;
Rozovsky, I ;
Stahl, N ;
Yancopoulos, GD ;
Greenberg, ME .
SCIENCE, 1997, 278 (5337) :477-483
[6]   GROWTH OF A RAT NEUROBLASTOMA CELL LINE IN SERUM-FREE SUPPLEMENTED MEDIUM [J].
BOTTENSTEIN, JE ;
SATO, GH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (01) :514-517
[7]  
Chaudhry AZ, 1997, DEV DYNAM, V208, P313
[8]   Cyclic AMP inducibility of the myelin basic protein gene promoter requires the NF1 site [J].
Clark, RE ;
Miskimins, WK ;
Miskimins, R .
INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2002, 20 (02) :103-111
[9]   TISSUE-SPECIFIC DNA METHYLATION PATTERNS OF THE RAT GLIAL FIBRILLARY ACIDIC PROTEIN GENE [J].
CONDORELLI, DF ;
NICOLETTI, VG ;
BARRESI, V ;
CARUSO, A ;
CONTICELLO, S ;
DEVELLIS, J ;
STELLA, AMG .
JOURNAL OF NEUROSCIENCE RESEARCH, 1994, 39 (06) :694-707
[10]   Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum [J].
das Neves, L ;
Duchala, CS ;
Godinho, F ;
Haxhiu, MA ;
Colmenares, C ;
Macklin, WB ;
Campbell, CE ;
Butz, KG ;
Gronostajski, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (21) :11946-11951