Main determinants of presynaptic Ca2+ dynamics at individual mossy fiber-CA3 pyramidal cell synapses

J Neurosci. 2006 Jun 28;26(26):7071-81. doi: 10.1523/JNEUROSCI.0946-06.2006.

Abstract

Synaptic transmission between hippocampal mossy fibers (MFs) and CA3 pyramidal cells exhibits remarkable use-dependent plasticity. The underlying presynaptic mechanisms, however, remain poorly understood. Here, we have used fluorescent Ca2+ indicators Fluo-4, Fluo-5F, and Oregon Green BAPTA-1 to investigate Ca2+ dynamics in individual giant MF boutons (MFBs) in area CA3 traced from the somata of granule cells held in whole-cell mode. In an individual MFB, a single action potential induces a brief peak of free Ca2+ (estimated in the range of 8-9 microm) followed by an elevation to approximately 320 nm, which slowly decays to its resting level of approximately 110 nm. Changes in the somatic membrane potential influence presynaptic Ca2+ entry at proximal MFBs in the hilus. This influence decays with distance along the axon, with a length constant of approximately 200 microm. In giant MFBs in CA3, progressive saturation of endogenous Ca2+ buffers during repetitive spiking amplifies rapid Ca2+ peaks and the residual Ca2+ severalfold, suggesting a causal link to synaptic facilitation. We find that internal Ca2+ stores contribute to maintaining the low resting Ca2+ providing approximately 22% of the buffering/extrusion capacity of giant MFBs. Rapid Ca2+ release from stores represents up to 20% of the presynaptic Ca2+ transient evoked by a brief train of action potentials. The results identify the main components of presynaptic Ca2+ dynamics at this important cortical synapse.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials
  • Animals
  • Axons / physiology
  • Calcium / metabolism*
  • Electrophysiology
  • In Vitro Techniques
  • Kinetics
  • Male
  • Models, Neurological
  • Mossy Fibers, Hippocampal / physiology*
  • Neuronal Plasticity
  • Osmolar Concentration
  • Presynaptic Terminals / metabolism*
  • Pyramidal Cells / physiology*
  • Rats
  • Rats, Sprague-Dawley
  • Signal Transduction / physiology
  • Synapses / metabolism*
  • Synaptic Transmission
  • Time Factors

Substances

  • Calcium