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Target Cell-Specific Involvement of Presynaptic Mitochondria in Post-Tetanic Potentiation at Hippocampal Mossy Fiber Synapses

机译:海马生苔藓纤维突触的强直后增强突触前线粒体的靶细胞特定参与。

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摘要

Previous studies indicate that boutons from the same axon exhibit distinct Ca2+ dynamics depending on the postsynaptic targets. Mossy fibers of hippocampal granule cells innervate synaptic targets via morphologically distinct boutons. We investigated mitochondrial involvement in the generation of post-tetanic residual Ca2+ (Cares) at large and small en passant mossy fiber boutons (MFBs). Mitochondria limited the [Ca2+]i build-up during high-frequency stimulation (HFS) at large MFBs, but not at small MFBs. The amount of Cares, quantified as a time integral of residual [Ca2+]i, was significantly larger at large MFBs than at small MFBs, and that at large MFBs was substantially attenuated by inhibitors of mitochondrial Ca2+ uniporter and mitochondrial Na+/Ca2+ exchanger (mitoNCX). In contrast, blockers of mitoNCX had no effect on the Cares at small MFBs. Post-tetanic Cares has been proposed as a mechanism for post-tetanic potentiation (PTP). We examined mitochondrial involvement in PTP at mossy fiber synapses on hilar mossy cells (MF→MC synapse) and on hilar interneurons (MF→HI synapse), which are presumably innervated via large and small MFBs, respectively. Consistent with the differential contribution of mitochondria to Cares at large and small MFBs, mitoNCX blockers significantly reduced the PTP at the MF→MC synapse, but not at the MF→HI synapse. In contrast, protein kinase C (PKC) inhibitors significantly reduced the PTP at MF→HI synapse, but not at the MF→MC synapse. These results indicate that mitochondria- and PKC-dependent PTP are expressed at distinct hilar mossy fiber synapses depending on postsynaptic targets.
机译:先前的研究表明,取决于突触后靶标,来自相同轴突的钮扣具有不同的Ca 2 + 动态。海马颗粒细胞的苔藓纤维通过形态学上不同的钮扣支配突触靶标。我们调查了线粒体在大,小整个生苔藓纤维钮扣(MFBs)中产生的破伤风残留Ca 2 + (Cares)的过程。线粒体限制了在大型MFB的高频刺激(HFS)期间[Ca 2 + ] i的积累,但在小型MFB却没有。 Cares的数量(以残留[Ca 2 + ] i的时间积分来量化)在大型MFB处明显大于在小型MFB处,并且在大型MFB处被线粒体Ca抑制剂大大削弱了 2 + 单向转运体和线粒体Na + / Ca 2 + 交换子(mitoNCX)。相比之下,mitoNCX的阻滞剂对小型MFB的Cares没有影响。已提出将强直性护理作为强直性增强作用(PTP)的机制。我们检查了线粒体参与PTP的高丝苔藓细胞(MF→MC突触)和高丝中间神经元(MF→HI突触)的苔藓纤维突触,推测它们分别通过大和小的MFB支配。与线粒体在大型和小型MFB上对Cares的不同贡献相一致,mitoNCX阻滞剂可显着降低MF→MC突触处的PTP,但不会降低MF→HI突触处的PTP。相反,蛋白激酶C(PKC)抑制剂可显着降低MF→HI突触处的PTP,但不会降低MF→MC突触处的PTP。这些结果表明,取决于突触后靶标,线粒体和PKC依赖性PTP在不同的肺门苔藓纤维突触中表达。

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