期刊
JOURNAL OF NEUROSCIENCE
卷 27, 期 50, 页码 13603-13613出版社
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.3985-07.2007
关键词
post-tetanic potentiation; residual calcium; mitochondria; hippocampal mossy fiber; hilar mossy cell; hilar interneuron
资金
- National Research Foundation of Korea [전06A1107] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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 Ca-res, 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 Ca-res at small MFBs. Post-tetanic Ca-res 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.
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