Ascorbate-induced differentiation of embryonic cortical precursors into neurons and astrocytes

被引:65
作者
Lee, JY [1 ]
Chang, MY
Park, CH
Kim, HY
Kim, JH
Son, H
Lee, YS
Lee, SH
机构
[1] Hanyang Univ, Dept Biochem, Coll Med, Seoul 133791, South Korea
[2] Hanyang Univ, Inst Mental Hlth, Seoul 133791, South Korea
[3] Hanyang Univ, Coll Med, Dept Microbiol, Seoul 133791, South Korea
[4] Hanyang Univ, Coll Med, Dept Physiol, Seoul 133791, South Korea
关键词
CNS precursors; CNS development; ascorbate; differentiation; synaptic maturation;
D O I
10.1002/jnr.10647
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A specific role for ascorbate (AA) in brain development has been postulated based on a rise of AA levels in fetal brain (Kratzing et al., 1985). To evaluate the role of AA during CNS development, we analyzed the survival, proliferation, and differentiation of AA-treated CNS precursor cells isolated from rat embryonic cortex. Immunocytochemical analyses revealed that AA promoted the in vitro differentiation of CNS precursor cells into neurons and astrocytes in a cell density-dependent manner. Additionally, AA increased the frequency and amplitude of miniature excitatory postsynaptic currents (mEPSCs) of postmitotic neurons in primary neuronal cultures. Differential expression analysis of genes specific to neuronal or glial differentiation revealed an AA-dependent increase in the expression of genes that could potentially compound the effects of AA on cell differentiation. These data suggest that AA may act in the developing brain to stimulate the generation of CNS neurons and glia, thereby assisting in the formation of neural circuits by promoting the acquisition of neuronal synaptic functions. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:156 / 165
页数:10
相关论文
共 52 条
[1]   Vitamin C crosses the blood-brain barrier in the oxidized form through the glucose transporters [J].
Agus, DB ;
Gambhir, SS ;
Pardridge, WM ;
Spielholz, C ;
Baselga, J ;
Vera, JC ;
Golde, DW .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2842-2848
[2]  
Brahma B, 2000, J NEUROCHEM, V74, P1263
[3]   OPTIMIZED SURVIVAL OF HIPPOCAMPAL-NEURONS IN B27-SUPPLEMENTED NEUROBASAL(TM), A NEW SERUM-FREE MEDIUM COMBINATION [J].
BREWER, GJ ;
TORRICELLI, JR ;
EVEGE, EK ;
PRICE, PJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 1993, 35 (05) :567-576
[4]   OXYGEN FREE-RADICAL INVOLVEMENT IN ISCHEMIA AND REPERFUSION INJURY TO BRAIN [J].
CAO, W ;
CARNEY, JM ;
DUCHON, A ;
FLOYD, RA ;
CHEVION, M .
NEUROSCIENCE LETTERS, 1988, 88 (02) :233-238
[5]  
CHANG MY, 2003, IN PRESS MOL CELL NE
[6]   ADRENOMEDULLARY CHROMAFFIN CELLS AS A MODEL TO STUDY THE NEUROBIOLOGY OF ASCORBIC-ACID - FROM MONOOXYGENATION TO NEUROMODULATION [J].
DILIBERTO, EJ ;
MENNITI, FS ;
KNOTH, J ;
DANIELS, AJ ;
KIZER, JS ;
VIVEROS, OH .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 498 :28-53
[7]   Bone morphogenetic proteins promote astroglial lineage commitment by mammalian subventricular zone progenitor cells [J].
Gross, RE ;
Mehler, MF ;
Mabie, PC ;
Zang, ZY ;
Santschi, L ;
Kessler, JA .
NEURON, 1996, 17 (04) :595-606
[8]   ASCORBIC-ACID IN THE BRAIN [J].
GRUNEWALD, RA .
BRAIN RESEARCH REVIEWS, 1993, 18 (01) :123-133
[9]  
Ha HC, 2000, CLIN CANCER RES, V6, P3783
[10]   ASCORBIC-ACID, METAL-IONS AND SUPEROXIDE RADICAL [J].
HALLIWELL, B ;
FOYER, CH .
BIOCHEMICAL JOURNAL, 1976, 155 (03) :697-700