Sánchez G, Ortega A
Departamento de Genética y Biología Molecular, Cinvestav-IPN, México D.F., Mexico.
Neuroreport. 1994 Oct 27;5(16):2109-12. doi: 10.1097/00001756-199410270-00030.
The effect of L-glutamate (L-Glu) and its structural analogs kainate (KA) and alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA) on the DNA binding activity of the activator protein 1 (AP-1) family of transcription factors was examined in cultured chick cerebellar Bergmann glia cells. These agonists evoked a dose- and time-dependent increase in AP-1 DNA binding activity and their responses were blocked by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX). The increase in DNA binding is probably mediated by an AMPA/low affinity KA subtype of L-Glu receptor. The synaptic localization of these receptors, their ion channel properties and a stimulus-transcription coupling further strengthen the putative role of glia cells in the modulation of synaptic efficacy and plasticity.
在培养的鸡小脑伯格曼胶质细胞中,研究了L-谷氨酸(L-Glu)及其结构类似物海藻酸(KA)和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)对转录因子激活蛋白1(AP-1)家族DNA结合活性的影响。这些激动剂引起AP-1 DNA结合活性呈剂量和时间依赖性增加,且它们的反应被6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)阻断。DNA结合的增加可能由L-谷氨酸受体的AMPA/低亲和力KA亚型介导。这些受体的突触定位、它们的离子通道特性以及刺激-转录偶联进一步强化了胶质细胞在调节突触效能和可塑性方面的假定作用。