Haak L L, Heller H C, van den Pol A N
Department of Biological Sciences, Stanford University, Stanford, California 94305-5020, USA.
J Neurosci. 1997 Mar 1;17(5):1825-37. doi: 10.1523/JNEUROSCI.17-05-01825.1997.
Although metabotropic glutamate receptor (mGluR) modulation has been studied extensively in neurons, it has not been investigated in astrocytes. We studied modulation of glutamate-evoked calcium rises in primary astrocyte cultures using fura-2 ratiometric digital calcium imaging. Calcium plays a key role as a second messenger system in astrocytes, both in regulation of many subcellular processes and in long distance intercellular signaling. Suprachiasmatic nucleus (SCN) and cortical astrocytes showed striking differences in sensitivity to glutamate and to mGluR agonists, even after several weeks in culture. Kainate-evoked intracellular calcium rises were inhibited by concurrent application of the type I and II mGluR agonists quisqualate (10 micro;M), trans-(+/-)-1-amino-1,3-cyclopentanedicarboxylate (100-500 micro;M), and (2S-1'S-2'S)-2-(carboxycyclopropyl)glycine (L-CCG-I) (10 micro;M). Inhibition mediated by L-CCG-I had long-lasting effects (>45 min) in approximately 30% of the SCN astrocytes tested. The inhibition could be mimicked by the L-type calcium channel blocker nimodipine (1 micro;M) as well as by protein kinase C (PKC) activators phorbol 12,13-dibutyrate (10 micro;M) and phorbol 12-myristate 13-acetate (500 nM), and blocked by the PKC inactivator (+/-)-1-(5-isoquinolinesulfonyl)-2-methylpiperazine (200 micro;M), suggesting a mechanism involving PKC modulation of L-type calcium channels. In contrast, mGluRs modulated serotonin (5HT)-evoked calcium rises through a different mechanism. The type III mGluR agonist L-2-amino-4-phosphonobutyrate consistently inhibited 5HT-evoked calcium rises, whereas in a smaller number of cells quisqualate and L-CCG-I showed both inhibitory and additive effects. Unlike the mGluR-kainate interaction, which required a pretreatment with an mGluR agonist and was insensitive to pertussis toxin (PTx), the mGluR modulation of 5HT actions was rapid and was blocked by PTx. These data suggest that glutamate, acting at several metabotropic receptors expressed by astrocytes, could modulate glial activity evoked by neurotransmitters and thereby influence the ongoing modulation of neurons by astrocytes.
尽管代谢型谷氨酸受体(mGluR)调节在神经元中已得到广泛研究,但在星形胶质细胞中尚未进行研究。我们使用fura-2比率数字钙成像技术研究了原代星形胶质细胞培养物中谷氨酸诱发的钙升高的调节。钙作为星形胶质细胞中的第二信使系统发挥关键作用,既参与许多亚细胞过程的调节,也参与长距离细胞间信号传导。即使在培养数周后,视交叉上核(SCN)和皮质星形胶质细胞对谷氨酸和mGluR激动剂的敏感性仍存在显著差异。同时应用I型和II型mGluR激动剂喹啉酸(10 μM)、反式(±)-1-氨基-1,3-环戊二羧酸(100 - 500 μM)和(2S-1'S-2'S)-2-(羧基环丙基)甘氨酸(L-CCG-I)(10 μM)可抑制海人酸诱发的细胞内钙升高。在约30%测试的SCN星形胶质细胞中,L-CCG-I介导的抑制具有长效作用(>45分钟)。L型钙通道阻滞剂尼莫地平(1 μM)以及蛋白激酶C(PKC)激活剂佛波醇12,13-二丁酸酯(10 μM)和佛波醇12-肉豆蔻酸13-乙酸酯(500 nM)可模拟这种抑制作用,而PKC失活剂(±)-1-(5-异喹啉磺酰基)-2-甲基哌嗪(200 μM)可阻断这种抑制作用,提示其机制涉及PKC对L型钙通道的调节。相比之下,mGluR通过不同机制调节5-羟色胺(5HT)诱发的钙升高。III型mGluR激动剂L-2-氨基-4-膦酸丁酸持续抑制5HT诱发的钙升高,而在少数细胞中,喹啉酸和L-CCG-I表现出抑制和相加作用。与mGluR-海人酸相互作用不同,后者需要用mGluR激动剂预处理且对百日咳毒素(PTx)不敏感,mGluR对5HT作用的调节迅速且被PTx阻断。这些数据表明,作用于星形胶质细胞表达的多种代谢型受体的谷氨酸,可调节神经递质诱发的胶质细胞活动,从而影响星形胶质细胞对神经元的持续调节。