Chisamore B, Solc M, Dow K
Department of Pediatrics, Kingston General Hospital, Queen's University, Canada.
Brain Res Dev Brain Res. 1996 Nov 22;97(1):22-8. doi: 10.1016/s0165-3806(96)00129-0.
Activity-dependent enduring change in cellular communication is essential for specific connectivity during development of the nervous system and for adaptive responses of the mature nervous system. Here we report that glutamate activation of excitatory amino acid receptors induces the synthesis and release of proteoglycans (PGs) from fetal hippocampal-astrocytes in dissociated culture. PG synthesis and release are mediated via kainate and metabotropic receptor activation. Glutamate exposure did not regulate the release of a specific family of PG, but glutamate inhibited the synthesis of heparan sulfate (HS) PGs that appeared within the extracellular environment of the astrocyte. Particulate protein kinase C (PKC) activity was increased by glutamate and the PKC activator phorbol 10-myristate 13-acetate produced a dose-dependent increase in PG release. However, glutamate-induced PG release was not blocked by inhibition of PKC activity. These data suggest that PKC activation can lead to PG release, but is not necessary for it. Activity-dependent influences on a class of substrate-bound molecular species with growth-modulatory properties may be involved in spatial regulation of neuronal growth responses produced by excitatory amino acids.
在神经系统发育过程中,依赖于活动的细胞通讯持久变化对于特定的连接形成至关重要,对于成熟神经系统的适应性反应也同样重要。在此我们报告,在解离培养中,兴奋性氨基酸受体的谷氨酸激活可诱导胎儿海马星形胶质细胞合成并释放蛋白聚糖(PGs)。PG的合成和释放是通过海人酸和代谢型受体激活介导的。谷氨酸暴露并未调节特定PG家族的释放,但谷氨酸抑制了在星形胶质细胞细胞外环境中出现的硫酸乙酰肝素(HS)PGs的合成。谷氨酸增加了颗粒蛋白激酶C(PKC)的活性,并且PKC激活剂佛波醇10 - 肉豆蔻酸酯13 - 乙酸酯使PG释放呈剂量依赖性增加。然而,谷氨酸诱导的PG释放并未被PKC活性抑制所阻断。这些数据表明PKC激活可导致PG释放,但并非其释放所必需。对一类具有生长调节特性的底物结合分子种类的活动依赖性影响可能参与了由兴奋性氨基酸产生的神经元生长反应的空间调节。