Estimation of nonuniform quantal parameters with multiple-probability fluctuation analysis: theory, application and limitations

Synapses are a key determinant of information processing in the central nervous system. Investigation of the mechanisms underlying synaptic transmission at central synapses is complicated by the inaccessibility of synaptic contacts and the fact that their temporal dynamics are governed by multiple parameters. Multiple-probability fluctuation analysis (MPFA) is a recently developed method for estimating quantal parameters from the variance and mean amplitude of evoked steady-state synaptic responses recorded under a range of release probability conditions. This article describes the theoretical basis and the underlying assumptions of MPFA, illustrating how a simplified multinomial model can be used to estimate mean quantal parameters at synapses where quantal size and release probability are nonuniform. Interpretations of the quantal parameter estimates are discussed in relation to uniquantal and multiquantal models of transmission. Practical aspects of this method are illustrated including a new method for estimating quantal size and variability, approaches for optimising data collection, error analysis and a method for identifying multivesicular release. The advantages and limitations of investigating synaptic function with MPFA are explored and contrasted with those for traditional quantal analysis and more recent optical quantal analysis methods.

[1]  E. Neher,et al.  Estimating Transmitter Release Rates from Postsynaptic Current Fluctuations , 2001, The Journal of Neuroscience.

[2]  L. Trussell,et al.  Minimizing Synaptic Depression by Control of Release Probability , 2001, The Journal of Neuroscience.

[3]  O. Prange,et al.  Amplification of calcium signals at dendritic spines provides a method for CNS quantal analysis. , 1999, Canadian journal of physiology and pharmacology.

[4]  Trese Leinders-Zufall,et al.  Divalent cations activate small- (SK) and large-conductance (BK) channels in mouse neuroblastoma cells: selective activation of SK channels by cadmium , 1992, Pflügers Archiv.

[5]  C. Reid,et al.  Postsynaptic expression of long‐term potentiation in the rat dentate gyrus demonstrated by variance‐mean analysis , 1999, The Journal of physiology.

[6]  J. C. Lodder,et al.  Large amplitude variability of GABAergic IPSCs in melanotropes from Xenopus laevis: evidence that quantal size differs between synapses. , 1994, Journal of neurophysiology.

[7]  Anatol C. Kreitzer,et al.  Interaction of Postsynaptic Receptor Saturation with Presynaptic Mechanisms Produces a Reliable Synapse , 2002, Neuron.

[8]  M. Kuno Quantal components of excitatory synaptic potentials in spinal motoneurones , 1964, The Journal of physiology.

[9]  C. Stevens,et al.  The kinetics of transmitter release at the frog neuromuscular junction , 1972, The Journal of physiology.

[10]  M. D. Miyamoto Binomial analysis of quantal transmitter release at glycerol treated frog neuromuscular junctions. , 1975, The Journal of physiology.

[11]  Colin Rose,et al.  Mathematical Statistics with Mathematica , 2002 .

[12]  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.

[13]  R. Fesce,et al.  Miniature endplate potential frequency and amplitude determined by an extension of Campbell's theorem. , 1985, Biophysical journal.

[14]  S. Redman Quantal analysis of synaptic potentials in neurons of the central nervous system. , 1990, Physiological reviews.

[15]  Jeffrey S. Diamond,et al.  Asynchronous release of synaptic vesicles determines the time course of the AMPA receptor-mediated EPSC , 1995, Neuron.

[16]  B. Katz,et al.  Quantal components of the end‐plate potential , 1954, The Journal of physiology.

[17]  R. Silver,et al.  Locus of frequency‐dependent depression identified with multiple‐probability fluctuation analysis at rat climbing fibre‐Purkinje cell synapses , 1998, The Journal of physiology.

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

[19]  Antonio Malgaroli,et al.  Loose-patch recordings of single quanta at individual hippocampal synapses , 1997, Nature.

[20]  J. Jack,et al.  The components of synaptic potentials evoked in cat spinal motoneurones by impulses in single group Ia afferents. , 1981, The Journal of physiology.

[21]  J. Clements,et al.  Unveiling synaptic plasticity: a new graphical and analytical approach , 2000, Trends in Neurosciences.

[22]  B. Walmsley Interpretation of ‘quantal’ peaks in distributions of evoked synaptic transmission at central synapses , 1995, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[23]  M. Bennett,et al.  The effect of calcium ions on the secretion of quanta evoked by an impulse at nerve terminal release sites , 1979, The Journal of general physiology.

[24]  K L Magleby,et al.  Facilitation, augmentation, and potentiation of transmitter release. , 1979, Progress in brain research.

[25]  B. Katz,et al.  Membrane Noise produced by Acetylcholine , 1970, Nature.

[26]  C. Stevens,et al.  Voltage clamp analysis of acetylcholine produced end‐plate current fluctuations at frog neuromuscular junction , 1973, The Journal of physiology.

[27]  B. Katz The release of neural transmitter substances , 1969 .

[28]  W. Denk,et al.  Mechanisms of Calcium Influx into Hippocampal Spines: Heterogeneity among Spines, Coincidence Detection by NMDA Receptors, and Optical Quantal Analysis , 1999, The Journal of Neuroscience.

[29]  D. Rossi,et al.  Spillover-Mediated Transmission at Inhibitory Synapses Promoted by High Affinity α6 Subunit GABAA Receptors and Glomerular Geometry , 1998, Neuron.

[30]  B. Walmsley,et al.  Release probability modulates short‐term plasticity at a rat giant terminal , 2000, The Journal of physiology.

[31]  T. Sejnowski,et al.  Heterogeneous Release Properties of Visualized Individual Hippocampal Synapses , 1997, Neuron.

[32]  M. Frerking,et al.  Effects of variance in mini amplitude on stimulus-evoked release: a comparison of two models. , 1996, Biophysical journal.

[33]  B. Walmsley,et al.  Counting quanta: Direct measurements of transmitter release at a central synapse , 1995, Neuron.

[34]  J. Clements Variance–mean analysis: a simple and reliable approach for investigating synaptic transmission and modulation , 2003, Journal of Neuroscience Methods.

[35]  B. Walmsley,et al.  Nonuniform release probabilities underlie quantal synaptic transmission at a mammalian excitatory central synapse. , 1988, Journal of neurophysiology.

[36]  F. Sigworth The variance of sodium current fluctuations at the node of Ranvier , 1980, The Journal of physiology.

[37]  J. Wolfowitz,et al.  Introduction to the Theory of Statistics. , 1951 .

[38]  J. Rothman,et al.  The use of pHluorins for optical measurements of presynaptic activity. , 2000, Biophysical journal.

[39]  C. Jahr,et al.  Multivesicular Release at Climbing Fiber-Purkinje Cell Synapses , 2001, Neuron.

[40]  D. Faber,et al.  Central synapses : quantal mechanisms and plasticity , 1998 .

[41]  R. Tsien,et al.  Variability of Neurotransmitter Concentration and Nonsaturation of Postsynaptic AMPA Receptors at Synapses in Hippocampal Cultures and Slices , 1999, Neuron.

[42]  R. Silver,et al.  Synaptic connections between layer 4 spiny neurone‐ layer 2/3 pyramidal cell pairs in juvenile rat barrel cortex: physiology and anatomy of interlaminar signalling within a cortical column , 2002, The Journal of physiology.

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

[44]  D. Kullmann,et al.  Extrasynaptic glutamate spillover in the hippocampus: evidence and implications , 1998, Trends in Neurosciences.

[45]  Christian Rosenmund,et al.  Nonuniform probability of glutamate release at a hippocampal synapse. , 1993, Science.

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

[47]  R. Malinow,et al.  The probability of transmitter release at a mammalian central synapse , 1993, Nature.

[48]  J J Jack,et al.  Quantal analysis of excitatory synaptic mechanisms in the mammalian central nervous system. , 1990, Cold Spring Harbor symposia on quantitative biology.

[49]  D. Quastel,et al.  The binomial model in fluctuation analysis of quantal neurotransmitter release. , 1997, Biophysical journal.

[50]  K. Svoboda,et al.  Facilitation at single synapses probed with optical quantal analysis , 2002, Nature Neuroscience.

[51]  Y. Sahara,et al.  Quantal components of the excitatory postsynaptic currents at a rat central auditory synapse , 2001, The Journal of physiology.

[52]  E. Neher,et al.  Separation of Presynaptic and Postsynaptic Contributions to Depression by Covariance Analysis of Successive EPSCs at the Calyx of Held Synapse , 2002, The Journal of Neuroscience.

[53]  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.

[54]  T. A. Ryan,et al.  Measurements of vesicle recycling in central neurons. , 2001, News in physiological sciences : an international journal of physiology produced jointly by the International Union of Physiological Sciences and the American Physiological Society.

[55]  Franklin A. Graybill,et al.  Introduction to the Theory of Statistics, 3rd ed. , 1974 .

[56]  A. C. Meyer,et al.  Estimation of Quantal Size and Number of Functional Active Zones at the Calyx of Held Synapse by Nonstationary EPSC Variance Analysis , 2001, The Journal of Neuroscience.

[57]  E. Neher,et al.  Estimating synaptic parameters from mean, variance, and covariance in trains of synaptic responses. , 2001, Biophysical journal.

[58]  R. Silver,et al.  Spillover of Glutamate onto Synaptic AMPA Receptors Enhances Fast Transmission at a Cerebellar Synapse , 2002, Neuron.

[59]  H. Clamann,et al.  Variance analysis of excitatory postsynaptic potentials in cat spinal motoneurons during posttetanic potentiation. , 1989, Journal of neurophysiology.

[60]  C. Jahr,et al.  Receptor Occupancy Limits Synaptic Depression at Climbing Fiber Synapses , 2003, The Journal of Neuroscience.

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

[62]  Y. Humeau,et al.  Rac GTPase Plays an Essential Role in Exocytosis by Controlling the Fusion Competence of Release Sites , 2002, The Journal of Neuroscience.