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

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.

[1]  H. Lüdi,et al.  The interrelations between the transport of sodium and calcium in mitochondria of various mammalian tissues. , 1978, European journal of biochemistry.

[2]  D. Attwell,et al.  The timing of channel opening during miniature end-plate currents , 1981, Brain Research.

[3]  D. Amaral,et al.  Development of the mossy fibers of the dentate gyrus: I. A light and electron microscopic study of the mossy fibers and their expansions , 1981, The Journal of comparative neurology.

[4]  T. Aiuchi,et al.  Effects of probes of membrane potential on metabolism in synaptosomes. , 1985, Biochimica et biophysica acta.

[5]  T. Gunter,et al.  Kinetics of mitochondrial calcium transport. II. A kinetic description of the sodium-dependent calcium efflux mechanism of liver mitochondria and inhibition by ruthenium red and by tetraphenylphosphonium. , 1986, The Journal of biological chemistry.

[6]  V. Zinchenko,et al.  TPP+ inhibits Na+-stimulated Ca2+ efflux from brain mitochondria. , 1986, Cell calcium.

[7]  D. Amaral,et al.  A light and electron microscopic analysis of the mossy fibers of the rat dentate gyrus , 1986, The Journal of comparative neurology.

[8]  E. Neher,et al.  Calcium gradients and buffers in bovine chromaffin cells. , 1992, The Journal of physiology.

[9]  R. Zucker,et al.  Residual Ca2 + and short-term synaptic plasticity , 1994, Nature.

[10]  D W Tank,et al.  The role of presynaptic calcium in short-term enhancement at the hippocampal mossy fiber synapse , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[11]  Paul Antoine Salin,et al.  Distinct short-term plasticity at two excitatory synapses in the hippocampus. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[12]  B. Sakmann,et al.  Calcium dynamics associated with a single action potential in a CNS presynaptic terminal. , 1997, Biophysical journal.

[13]  R. Zucker,et al.  Mitochondrial Involvement in Post-Tetanic Potentiation of Synaptic Transmission , 1997, Neuron.

[14]  W. Regehr Interplay between sodium and calcium dynamics in granule cell presynaptic terminals. , 1997, Biophysical journal.

[15]  E. Barrett,et al.  Stimulation‐induced changes in [ca2+] in lizard motor nerve terminals , 1997, The Journal of physiology.

[16]  E. Barrett,et al.  Evidence that mitochondria buffer physiological Ca2+ loads in lizard motor nerve terminals , 1998, The Journal of physiology.

[17]  G Buzsáki,et al.  GABAergic Cells Are the Major Postsynaptic Targets of Mossy Fibers in the Rat Hippocampus , 1998, The Journal of Neuroscience.

[18]  N Spruston,et al.  Specialized electrophysiological properties of anatomically identified neurons in the hilar region of the rat fascia dentata. , 1998, Journal of neurophysiology.

[19]  P. Bernardi,et al.  Mitochondrial transport of cations: channels, exchangers, and permeability transition. , 1999, Physiological reviews.

[20]  E. Barrett,et al.  Stimulation-Evoked Increases in Cytosolic [Ca2+] in Mouse Motor Nerve Terminals Are Limited by Mitochondrial Uptake and Are Temperature-Dependent , 2000, The Journal of Neuroscience.

[21]  S. H. Lee,et al.  Differences in Ca2+ buffering properties between excitatory and inhibitory hippocampal neurons from the rat , 2000, The Journal of physiology.

[22]  K. Tóth,et al.  Target‐specific expression of pre‐ and postsynaptic mechanisms , 2000, The Journal of physiology.

[23]  K. Svoboda,et al.  Estimating intracellular calcium concentrations and buffering without wavelength ratioing. , 2000, Biophysical journal.

[24]  P. Jonas,et al.  PTP and LTP at a hippocampal mossy fiber-interneuron synapse , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[25]  R. Zucker,et al.  Roles for Mitochondrial and Reverse Mode Na+/Ca2+ Exchange and the Plasmalemma Ca2+ ATPase in Post-Tetanic Potentiation at Crayfish Neuromuscular Junctions , 2001, The Journal of Neuroscience.

[26]  B. Sakmann,et al.  Transmitter release modulation by intracellular Ca2+ buffers in facilitating and depressing nerve terminals of pyramidal cells in layer 2/3 of the rat neocortex indicates a target cell‐specific difference in presynaptic calcium dynamics , 2001, The Journal of physiology.

[27]  E. Neher,et al.  Combining Deconvolution and Noise Analysis for the Estimation of Transmitter Release Rates at the Calyx of Held , 2001, The Journal of Neuroscience.

[28]  K. Svoboda,et al.  The Life Cycle of Ca2+ Ions in Dendritic Spines , 2002, Neuron.

[29]  M. Osanai,et al.  Ca2+-Dependent Ca2+ Clearance Via Mitochondrial Uptake and Plasmalemmal Extrusion in Frog Motor Nerve Terminals , 2002 .

[30]  I. Forsythe,et al.  Presynaptic Mitochondrial Calcium Sequestration Influences Transmission at Mammalian Central Synapses , 2002, The Journal of Neuroscience.

[31]  G. Buzsáki,et al.  Single granule cells reliably discharge targets in the hippocampal CA3 network in vivo , 2002, Nature Neuroscience.

[32]  M. Osanai,et al.  Ca(2+)-dependent Ca(2+) clearance via mitochondrial uptake and plasmalemmal extrusion in frog motor nerve terminals. , 2002, Journal of neurophysiology.

[33]  W. Regehr,et al.  Short-term synaptic plasticity. , 2002, Annual review of physiology.

[34]  Scott M Thompson,et al.  Activity-dependent activation of presynaptic protein kinase C mediates post-tetanic potentiation , 2003, Nature Neuroscience.

[35]  P. Jonas,et al.  A large pool of releasable vesicles in a cortical glutamatergic synapse , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[36]  Maria Blatow,et al.  Ca2+ Buffer Saturation Underlies Paired Pulse Facilitation in Calbindin-D28k-Containing Terminals , 2003, Neuron.

[37]  W. Ho,et al.  Distribution of K+-Dependent Na+/Ca2+ Exchangers in the Rat Supraoptic Magnocellular Neuron Is Polarized to Axon Terminals , 2003, The Journal of Neuroscience.

[38]  David E. Clapham,et al.  The mitochondrial calcium uniporter is a highly selective ion channel , 2004, Nature.

[39]  L. Abbott,et al.  Synaptic computation , 2004, Nature.

[40]  W. Ho,et al.  Li+ enhances GABAergic inputs to granule cells in the rat hippocampal dentate gyrus , 2004, Neuropharmacology.

[41]  R. Zucker,et al.  Facilitation through buffer saturation: constraints on endogenous buffering properties. , 2004, Biophysical journal.

[42]  Jerson L. Silva,et al.  Reversible aggregation plays a crucial role on the folding landscape of p53 core domain. , 2004, Biophysical journal.

[43]  Urs Gerber,et al.  A frequency-dependent switch from inhibition to excitation in a hippocampal unitary circuit , 2004, Nature.

[44]  W. Ho,et al.  Interplay between Na+/Ca2+ Exchangers and Mitochondria in Ca2+ Clearance at the Calyx of Held , 2005, The Journal of Neuroscience.

[45]  Dietmar Schmitz,et al.  Synaptic plasticity at hippocampal mossy fibre synapses , 2005, Nature Reviews Neuroscience.

[46]  D. Johnston,et al.  Target Cell-Dependent Normalization of Transmitter Release at Neocortical Synapses , 2005, Science.

[47]  P. Kostyuk,et al.  Possible role of mitochondria in posttetanic potentiation of GABAergic synaptic transmission in rat neocortical cell cultures , 2005, Synapse.

[48]  Dirk Dietrich,et al.  Endogenous Ca2+ Buffer Concentration and Ca2+ Microdomains in Hippocampal Neurons , 2005, The Journal of Neuroscience.

[49]  I. Soltesz,et al.  Long‐ and short‐term plasticity at mossy fiber synapses on mossy cells in the rat dentate gyrus , 2005, Hippocampus.

[50]  J. Borst,et al.  Post‐tetanic potentiation in the rat calyx of Held synapse , 2005, The Journal of physiology.

[51]  R. Schneggenburger,et al.  Presynaptic Ca2+ Requirements and Developmental Regulation of Posttetanic Potentiation at the Calyx of Held , 2005, The Journal of Neuroscience.

[52]  J. Lacaille,et al.  Compartmentalized Ca2+ Channel Regulation at Divergent Mossy-Fiber Release Sites Underlies Target Cell-Dependent Plasticity , 2006, Neuron.

[53]  E. Barrett,et al.  Extrusion of Ca2+ from mouse motor terminal mitochondria via a Na+–Ca2+ exchanger increases post‐tetanic evoked release , 2006, The Journal of physiology.

[54]  M. Frotscher,et al.  Timing and efficacy of transmitter release at mossy fiber synapses in the hippocampal network , 2006, Pflügers Archiv.

[55]  Pico Caroni,et al.  Long-Term Rearrangements of Hippocampal Mossy Fiber Terminal Connectivity in the Adult Regulated by Experience , 2006, Neuron.

[56]  Urs Gerber,et al.  Recruitment of an inhibitory hippocampal network after bursting in a single granule cell , 2007, Proceedings of the National Academy of Sciences.

[57]  M. Verhage,et al.  Interdependence of PKC-Dependent and PKC-Independent Pathways for Presynaptic Plasticity , 2007, Neuron.

[58]  W. Regehr,et al.  Differential Expression of Posttetanic Potentiation and Retrograde Signaling Mediate Target-Dependent Short-Term Synaptic Plasticity , 2007, Neuron.