Ca2+ influx through AMPA or kainate receptors alone is sufficient to initiate excitotoxicity in cultured oligodendrocytes

被引:101
作者
Alberdi, E [1 ]
Sánchez-Gómez, MV [1 ]
Marino, A [1 ]
Matute, C [1 ]
机构
[1] Univ Basque Country, Dept Neurociencias, E-48940 Leioa, Vizcaya, Spain
关键词
D O I
10.1006/nbdi.2001.0457
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oligodendrocytes are vulnerable to excitotoxic insults mediated by AMPA receptors and by low and high affinity kainate receptors, a feature that is dependent on Ca2+ influx. In the current study, we have analyzed the intracellular concentration of calcium [Ca2+](i) as well as the entry routes of this cation, upon activation of these receptors. Selective activation of either receptor type resulted in a substantial increase (up to fivefold) of [Ca2+](i), an effect which was totally abolished by the non-NMDA receptor antagonist CNOX or by removing Ca2+ from the culture medium. Blockade of voltage-gated Ca2+ channels with La3+ or nifedipine, reduced the amplitude of the Ca2+ current triggered by AMPA receptor activation by similar to65%, but not that initiated by low and high affinity kainate receptors. In contrast, KB-R7943, an inhibitor of the plasma membrane Na+-Ca2+ exchanger, solely attenuated the rise in [Ca2+] by similar to25% due to activation of low affinity kainate receptors. However, oligodendroglial death by glutamate receptor overactivation was largely unaffected in the presence of La3+ or KB-R7943. These findings indicate that Ca2+ influx via AMPA and kainate receptors alone is sufficient to initiate cell death in oligodendrocytes, which does not require the entry of calcium via other routes such as voltage-activated calcium channels or the plasma membrane Na+-Ca2+ exchanger. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:234 / 243
页数:10
相关论文
共 50 条
[1]   CELL-DEATH AND CONTROL OF CELL-SURVIVAL IN THE OLIGODENDROCYTE LINEAGE [J].
BARRES, BA ;
HART, IK ;
COLES, HSR ;
BURNE, JF ;
VOYYODIC, JT ;
RICHARDSON, WD ;
RAFF, MC .
CELL, 1992, 70 (01) :31-46
[2]  
BARRES BA, 1990, ANNU REV NEUROSCI, V13, P441, DOI 10.1146/annurev.ne.13.030190.002301
[3]  
Canzoniero LMT, 1996, J NEUROSCI RES, V45, P226
[4]  
Carriedo SG, 1998, J NEUROSCI, V18, P7727
[5]  
Choi Dennis W., 1995, Trends in Neurosciences, V18, P58, DOI 10.1016/0166-2236(95)93870-4
[6]   Reduced editing of low-affinity kainate receptor subunits in optic nerve glial cells [J].
de Zulueta, MP ;
Matute, C .
MOLECULAR BRAIN RESEARCH, 1999, 73 (1-2) :104-109
[7]  
Dingledine R, 1999, PHARMACOL REV, V51, P7
[8]   Rapid ischemic cell death in immature oligodendrocytes:: A fatal glutamate release feedback loop [J].
Fern, R ;
Möller, T .
JOURNAL OF NEUROSCIENCE, 2000, 20 (01) :34-42
[9]   Expression of kainate-selective glutamate receptor subunits in glial cells of the adult bovine white matter [J].
GarciaBarcina, JM ;
Matute, C .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (11) :2379-2387
[10]  
GOLDMAN WF, 1994, J NEUROSCI, V14, P5834