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Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity

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  • Bernhard Nessler
  • Michael Pfeiffer
  • Lars Buesing
  • Wolfgang Maass

Abstract

The principles by which networks of neurons compute, and how spike-timing dependent plasticity (STDP) of synaptic weights generates and maintains their computational function, are unknown. Preceding work has shown that soft winner-take-all (WTA) circuits, where pyramidal neurons inhibit each other via interneurons, are a common motif of cortical microcircuits. We show through theoretical analysis and computer simulations that Bayesian computation is induced in these network motifs through STDP in combination with activity-dependent changes in the excitability of neurons. The fundamental components of this emergent Bayesian computation are priors that result from adaptation of neuronal excitability and implicit generative models for hidden causes that are created in the synaptic weights through STDP. In fact, a surprising result is that STDP is able to approximate a powerful principle for fitting such implicit generative models to high-dimensional spike inputs: Expectation Maximization. Our results suggest that the experimentally observed spontaneous activity and trial-to-trial variability of cortical neurons are essential features of their information processing capability, since their functional role is to represent probability distributions rather than static neural codes. Furthermore it suggests networks of Bayesian computation modules as a new model for distributed information processing in the cortex. Author Summary: How do neurons learn to extract information from their inputs, and perform meaningful computations? Neurons receive inputs as continuous streams of action potentials or “spikes” that arrive at thousands of synapses. The strength of these synapses - the synaptic weight - undergoes constant modification. It has been demonstrated in numerous experiments that this modification depends on the temporal order of spikes in the pre- and postsynaptic neuron, a rule known as STDP, but it has remained unclear, how this contributes to higher level functions in neural network architectures. In this paper we show that STDP induces in a commonly found connectivity motif in the cortex - a winner-take-all (WTA) network - autonomous, self-organized learning of probabilistic models of the input. The resulting function of the neural circuit is Bayesian computation on the input spike trains. Such unsupervised learning has previously been studied extensively on an abstract, algorithmical level. We show that STDP approximates one of the most powerful learning methods in machine learning, Expectation-Maximization (EM). In a series of computer simulations we demonstrate that this enables STDP in WTA circuits to solve complex learning tasks, reaching a performance level that surpasses previous uses of spiking neural networks.

Suggested Citation

  • Bernhard Nessler & Michael Pfeiffer & Lars Buesing & Wolfgang Maass, 2013. "Bayesian Computation Emerges in Generic Cortical Microcircuits through Spike-Timing-Dependent Plasticity," PLOS Computational Biology, Public Library of Science, vol. 9(4), pages 1-30, April.
  • Handle: RePEc:plo:pcbi00:1003037
    DOI: 10.1371/journal.pcbi.1003037
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    References listed on IDEAS

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    1. Dejan Pecevski & Lars Buesing & Wolfgang Maass, 2011. "Probabilistic Inference in General Graphical Models through Sampling in Stochastic Networks of Spiking Neurons," PLOS Computational Biology, Public Library of Science, vol. 7(12), pages 1-25, December.
    2. Lars Buesing & Johannes Bill & Bernhard Nessler & Wolfgang Maass, 2011. "Neural Dynamics as Sampling: A Model for Stochastic Computation in Recurrent Networks of Spiking Neurons," PLOS Computational Biology, Public Library of Science, vol. 7(11), pages 1-22, November.
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    6. Robert C. Froemke & Yang Dan, 2002. "Spike-timing-dependent synaptic modification induced by natural spike trains," Nature, Nature, vol. 416(6879), pages 433-438, March.
    7. Richard H. R. Hahnloser & Rahul Sarpeshkar & Misha A. Mahowald & Rodney J. Douglas & H. Sebastian Seung, 2000. "Digital selection and analogue amplification coexist in a cortex-inspired silicon circuit," Nature, Nature, vol. 405(6789), pages 947-951, June.
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    Cited by:

    1. Matthieu Gilson & David Dahmen & Rubén Moreno-Bote & Andrea Insabato & Moritz Helias, 2020. "The covariance perceptron: A new paradigm for classification and processing of time series in recurrent neuronal networks," PLOS Computational Biology, Public Library of Science, vol. 16(10), pages 1-38, October.
    2. David Kappel & Bernhard Nessler & Wolfgang Maass, 2014. "STDP Installs in Winner-Take-All Circuits an Online Approximation to Hidden Markov Model Learning," PLOS Computational Biology, Public Library of Science, vol. 10(3), pages 1-22, March.
    3. Mingi Jeon & Taewook Kang & Jae-Jin Lee & Woojoo Lee, 2022. "A Study on the Low-Power Operation of the Spike Neural Network Using the Sensory Adaptation Method," Mathematics, MDPI, vol. 10(22), pages 1-19, November.
    4. Lieder, Falk & Griffiths, Tom & Hsu, Ming, 2016. "Over-representation of extreme events in decision-making reflects rational use of cognitive resources," OSF Preprints kxxag, Center for Open Science.
    5. Robert Legenstein & Wolfgang Maass, 2014. "Ensembles of Spiking Neurons with Noise Support Optimal Probabilistic Inference in a Dynamically Changing Environment," PLOS Computational Biology, Public Library of Science, vol. 10(10), pages 1-27, October.
    6. Martinez-Saito, Mario, 2022. "Discrete scaling and criticality in a chain of adaptive excitable integrators," Chaos, Solitons & Fractals, Elsevier, vol. 163(C).

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