Loose-patch recordings of single quanta at individual hippocampal synapses

Synapses in the central nervous system are typically studied by recording electrical responses from the cell body of the postsynaptic cell. Because neurons are normally connected by multiple synaptic contacts, these postsynaptic responses reflect the combined activity of many thousands synapses, and it remains unclear to what extent the properties of individual synapses can be deduced from the population response. We have therefore developed a method for recording the activity of individual hippocampal synapses. By capturing an isolated presynaptic bouton inside a loose-patch pipette and recording from the associated patch of postsynaptic membrane, we were able to detect miniature excitatory postsynaptic currents (‘minis’) arising from spontaneous vesicle exocytosis at a single synaptic site, and to compare these with minis recorded simultaneously from the cell body. The average peak conductance at a single synapse was about 900 pS, corresponding roughly to the opening of 90 AMPA-type glutamate-receptor channels. The variability in this conductance was about 30%, matching the value reported for the neuromuscular junction. Given that our synapses displayed single postsynaptic densities (PSDs), this variability is larger than would be predicted from the random opening of receptor channels, suggesting that they are not saturated by the content of a single vesicle. Therefore the response to a quantum of neurotransmitter at these synapses is not limited by the number of available postsynaptic receptors.

[1]  F. Edwards,et al.  Anatomy and electrophysiology of fast central synapses lead to a structural model for long-term potentiation. , 1995, Physiological reviews.

[2]  J. Jack,et al.  Electric current flow in excitable cells , 1975 .

[3]  B Sakmann,et al.  Quantal analysis of inhibitory synaptic transmission in the dentate gyrus of rat hippocampal slices: a patch‐clamp study. , 1990, The Journal of physiology.

[4]  M. Frerking,et al.  Saturation of postsynaptic receptors at central synapses? , 1996, Current Opinion in Neurobiology.

[5]  H Korn,et al.  Intrinsic quantal variability due to stochastic properties of receptor-transmitter interactions. , 1992, Science.

[6]  Stephen J. Smith,et al.  The kinetics of synaptic vesicle recycling measured at single presynaptic boutons , 1993, Neuron.

[7]  W. Almers,et al.  Quantal neurotransmitter release from early endosomes? , 1994, Trends in cell biology.

[8]  L. Stjärne Molecular and cellular mechanisms of neurotransmitter release , 1994 .

[9]  D. Faber,et al.  Inhibitory synaptic transmission in isolated patches of membrane from cultured rat spinal cord and medullary neurons. , 1996, Journal of neurophysiology.

[10]  N. Spruston,et al.  Voltage- and space-clamp errors associated with the measurement of electrotonically remote synaptic events. , 1993, Journal of neurophysiology.

[11]  R. Nicoll,et al.  Long-term potentiation is associated with increases in quantal content and quantal amplitude , 1992, Nature.

[12]  G. Major,et al.  Quantal analysis of the synaptic excitation of CA1 hippocampal pyramidal cells. , 1994, Advances in second messenger and phosphoprotein research.

[13]  R. Malinow,et al.  Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice , 1995, Nature.

[14]  Antonio Malgaroli,et al.  Glutamate-induced long-term potentiation of the frequency of miniature synaptic currents in cultured hippocampal neurons , 1992, Nature.

[15]  B. Sakmann,et al.  Quantal components of unitary EPSCs at the mossy fibre synapse on CA3 pyramidal cells of rat hippocampus. , 1993, The Journal of physiology.

[16]  R. Malinow,et al.  Direct measurement of quantal changes underlying long-term potentiation in CA1 hippocampus , 1992, Neuron.

[17]  J. Isaac,et al.  Evidence for silent synapses: Implications for the expression of LTP , 1995, Neuron.

[18]  K. Stratford,et al.  Quantal analysis of excitatory synaptic action and depression in hippocampal slices , 1991, Nature.

[19]  W. Almers,et al.  The Loose Patch Clamp , 1983 .

[20]  B. Sakmann,et al.  Single-Channel Recording , 1995, Springer US.

[21]  B. Katz,et al.  Spontaneous subthreshold activity at motor nerve endings , 1952, The Journal of physiology.

[22]  R. Silver,et al.  Non‐NMDA glutamate receptor occupancy and open probability at a rat cerebellar synapse with single and multiple release sites. , 1996, The Journal of physiology.

[23]  R. Tsien,et al.  Properties of synaptic transmission at single hippocampal synaptic boutons , 1995, Nature.

[24]  Shaul Hestrin,et al.  Activation and desensitization of glutamate-activated channels mediating fast excitatory synaptic currents in the visual cortex , 1992, Neuron.

[25]  C. Stevens,et al.  Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[26]  W. Betz,et al.  Optical analysis of synaptic vesicle recycling at the frog neuromuscular junction. , 1992, Science.

[27]  N. Spruston,et al.  Dendritic glutamate receptor channels in rat hippocampal CA3 and CA1 pyramidal neurons. , 1995, The Journal of physiology.

[28]  S. Redman,et al.  Statistical analysis of amplitude fluctuations in EPSCs evoked in rat CA1 pyramidal neurones in vitro. , 1996, The Journal of physiology.

[29]  R. Silver,et al.  Rapid-time-course miniature and evoked excitatory currents at cerebellar synapses in situ , 1992, Nature.

[30]  C. Stevens,et al.  NMDA and non-NMDA receptors are co-localized at individual excitatory synapses in cultured rat hippocampus , 1989, Nature.

[31]  D. Faber,et al.  The one-vesicle hypothesis and multivesicular release. , 1994, Advances in second messenger and phosphoprotein research.

[32]  A. Konnerth,et al.  Long-term potentiation and functional synapse induction in developing hippocampus , 1996, Nature.