Literature DB >> 20188660

Spike-time-dependent plasticity and heterosynaptic competition organize networks to produce long scale-free sequences of neural activity.

Ila R Fiete1, Walter Senn, Claude Z H Wang, Richard H R Hahnloser.   

Abstract

Sequential neural activity patterns are as ubiquitous as the outputs they drive, which include motor gestures and sequential cognitive processes. Neural sequences are long, compared to the activation durations of participating neurons, and sequence coding is sparse. Numerous studies demonstrate that spike-time-dependent plasticity (STDP), the primary known mechanism for temporal order learning in neurons, cannot organize networks to generate long sequences, raising the question of how such networks are formed. We show that heterosynaptic competition within single neurons, when combined with STDP, organizes networks to generate long unary activity sequences even without sequential training inputs. The network produces a diversity of sequences with a power law length distribution and exponent -1, independent of cellular time constants. We show evidence for a similar distribution of sequence lengths in the recorded premotor song activity of songbirds. These results suggest that neural sequences may be shaped by synaptic constraints and network circuitry rather than cellular time constants.

Mesh:

Year:  2010        PMID: 20188660     DOI: 10.1016/j.neuron.2010.02.003

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  115 in total

1.  Two distinct modes of forebrain circuit dynamics underlie temporal patterning in the vocalizations of young songbirds.

Authors:  Dmitriy Aronov; Lena Veit; Jesse H Goldberg; Michale S Fee
Journal:  J Neurosci       Date:  2011-11-09       Impact factor: 6.167

Review 2.  Packet-based communication in the cortex.

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Authors:  Alan Veliz-Cuba; Harel Z Shouval; Krešimir Josić; Zachary P Kilpatrick
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4.  Acute off-target effects of neural circuit manipulations.

Authors:  Timothy M Otchy; Steffen B E Wolff; Juliana Y Rhee; Cengiz Pehlevan; Risa Kawai; Alexandre Kempf; Sharon M H Gobes; Bence P Ölveczky
Journal:  Nature       Date:  2015-12-09       Impact factor: 49.962

5.  Neural encoding and integration of learned probabilistic sequences in avian sensory-motor circuitry.

Authors:  Kristofer E Bouchard; Michael S Brainard
Journal:  J Neurosci       Date:  2013-11-06       Impact factor: 6.167

Review 6.  Neural syntax: cell assemblies, synapsembles, and readers.

Authors:  György Buzsáki
Journal:  Neuron       Date:  2010-11-04       Impact factor: 17.173

Review 7.  A hypothesis for basal ganglia-dependent reinforcement learning in the songbird.

Authors:  M S Fee; J H Goldberg
Journal:  Neuroscience       Date:  2011-10-13       Impact factor: 3.590

8.  A model for complex sequence learning and reproduction in neural populations.

Authors:  Sergio Oscar Verduzco-Flores; Mark Bodner; Bard Ermentrout
Journal:  J Comput Neurosci       Date:  2011-09-02       Impact factor: 1.621

9.  Population-Level Representation of a Temporal Sequence Underlying Song Production in the Zebra Finch.

Authors:  Michel A Picardo; Josh Merel; Kalman A Katlowitz; Daniela Vallentin; Daniel E Okobi; Sam E Benezra; Rachel C Clary; Eftychios A Pnevmatikakis; Liam Paninski; Michael A Long
Journal:  Neuron       Date:  2016-05-18       Impact factor: 17.173

10.  Support for a synaptic chain model of neuronal sequence generation.

Authors:  Michael A Long; Dezhe Z Jin; Michale S Fee
Journal:  Nature       Date:  2010-10-24       Impact factor: 49.962

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