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首页> 外文期刊>The European Journal of Neuroscience >Characterization of the metabotropic glutamate receptors mediating phospholipase C activation and calcium release in cerebellar granule cells: calcium-dependence of the phospholipase C response.
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Characterization of the metabotropic glutamate receptors mediating phospholipase C activation and calcium release in cerebellar granule cells: calcium-dependence of the phospholipase C response.

机译:小脑颗粒细胞介导磷脂酶C活化和钙释放的代谢型谷氨酸受体的表征:磷脂酶C反应的钙依赖性。

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In this study we have determined the metabotropic glutamate receptors (mGluRs) involved in the glutamate activation of phospholipase C (PLC) and Ca(2+) mobilization in cerebellar granule cells at 9 days in vitro; and studied the Ca(2+) modulation of the PLC response. Both PLC activation and Ca(2+) signalling were found to be mediated exclusively by the mGluR1 subtype, although both group I mGluRs, mGluR1 alpha and mGluR5, could be detected in cell extracts. Exposure of cells to medium devoid of Ca(2+) for various times before agonist stimulation reduced the PLC response, which was quickly recovered following the re-exposure of cells to Ca(2+)-containing medium. The extent of the glutamate response correlated well with changes in the cytosolic Ca(2+) concentration. On the other hand, loading of the intracellular Ca(2+) stores by a transient depolarization followed by washing in nondepolarizing buffer, allowed glutamate to release stored Ca(2+) in the majority of cells and enhanced glutamate activation of PLC. Under such conditions, the absence of extracellular Ca(2+) during stimulation and the chelation of cytosolic Ca(2+) with BAPTA/AM inhibited both glutamate-elicited Ca(2+) response and PLC activation. Overall, these results indicate that the mGluR-mediated activation of PLC depends on the presence of extracellular Ca(2+) and can be modulated by moderate changes of cytosolic Ca(2+). Furthermore, ryanodine reduced PLC stimulation by glutamate in predepolarized cells but not in control cells, suggesting that ryanodine receptors could play a role in the potentiation of the mGluR-mediated activation of PLC by Ca(2+) release in predepolarized cells.
机译:在这项研究中,我们确定了代谢型谷氨酸受体(mGluRs)在体外第9天参与了小脑颗粒细胞中磷脂酶C(PLC)的谷氨酸活化和Ca(2+)的动员;并研究了PLC响应的Ca(2+)调制。发现PLC激活和Ca(2+)信号均仅由mGluR1亚型介导,尽管I组mGluRs,mGluR1α和mGluR5均可在细胞提取物中检测到。在激动剂刺激之前,将细胞暴露于无Ca(2+)的培养基中的时间长短不一,从而降低了PLC的响应,在将细胞重新暴露于含Ca(2+)的培养基后,PLC反应得以迅速恢复。谷氨酸反应的程度与胞质Ca(2+)浓度的变化相关性很好。另一方面,通过瞬时去极化随后在非去极化缓冲液中洗涤来加载细胞内Ca(2+)存储,使谷氨酸释放大部分细胞中的Ca(2+)并增强PLC的谷氨酸激活。在这种情况下,在刺激过程中不存在胞外Ca(2+)和与BAPTA / AM的胞质Ca(2+)螯合抑制谷氨酸引起的Ca(2+)反应和PLC激活。总体而言,这些结果表明,mGluR介导的PLC激活取决于细胞外Ca(2+)的存在,并且可以通过适度改变胞质Ca(2+)进行调节。此外,ryanodine减少了去极化前细胞中谷氨酸对PLC的刺激,但没有在对照细胞中,这表明ryanodine受体可能通过在去极化前细胞中的Ca(2+)释放而增强了mGluR介导的PLC活化。

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