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REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO

Many lines of evidence suggest that memory in the mammalian brain is stored with distinct spatiotemporal patterns(1,2). Despite recent progresses in identifying neuronal populations involved in memory coding(3–5), the synapse-level mechanism is still poorly understood. Computational models and elect...

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Autores principales: Fu, Min, Yu, Xinzhu, Lu, Ju, Zuo, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292711/
https://www.ncbi.nlm.nih.gov/pubmed/22343892
http://dx.doi.org/10.1038/nature10844
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author Fu, Min
Yu, Xinzhu
Lu, Ju
Zuo, Yi
author_facet Fu, Min
Yu, Xinzhu
Lu, Ju
Zuo, Yi
author_sort Fu, Min
collection PubMed
description Many lines of evidence suggest that memory in the mammalian brain is stored with distinct spatiotemporal patterns(1,2). Despite recent progresses in identifying neuronal populations involved in memory coding(3–5), the synapse-level mechanism is still poorly understood. Computational models and electrophysiological data have shown that functional clustering of synapses along dendritic branches leads to nonlinear summation of synaptic inputs and greatly expands the computing power of a neural network(6–10). However, whether neighboring synapses are involved in encoding similar memory and how task-specific cortical networks develop during learning remain elusive. Using transcranial two-photon microscopy(11), we followed apical dendrites of layer 5 (L5) pyramidal neurons in the motor cortex while mice practiced novel forelimb skills. Here we show that a third of new dendritic spines (postsynaptic structures of most excitatory synapses) formed during the acquisition phase of learning emerge in clusters, and the majority of such clusters are neighboring spine pairs. These clustered new spines are more likely to persist throughout prolonged learning sessions and even long after training stops, compared to non-clustered counterparts. Moreover, formation of new spine clusters requires repetition of the same motor task, and the emergence of succedent new spine(s) accompanies the strengthening of the first new spine in the cluster. We also show that under control conditions new spines appear to avoid existing stable spines, rather than being uniformly added along dendrites. However, succedent new spines in clusters overcome such a spatial constraint and form in close vicinity to neighboring stable spines. Our findings suggest that clustering of new synapses along dendrites is induced by repetitive activation of the cortical circuitry during learning, providing a structural basis for spatial coding of motor memory in the mammalian brain.
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spelling pubmed-32927112012-09-01 REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO Fu, Min Yu, Xinzhu Lu, Ju Zuo, Yi Nature Article Many lines of evidence suggest that memory in the mammalian brain is stored with distinct spatiotemporal patterns(1,2). Despite recent progresses in identifying neuronal populations involved in memory coding(3–5), the synapse-level mechanism is still poorly understood. Computational models and electrophysiological data have shown that functional clustering of synapses along dendritic branches leads to nonlinear summation of synaptic inputs and greatly expands the computing power of a neural network(6–10). However, whether neighboring synapses are involved in encoding similar memory and how task-specific cortical networks develop during learning remain elusive. Using transcranial two-photon microscopy(11), we followed apical dendrites of layer 5 (L5) pyramidal neurons in the motor cortex while mice practiced novel forelimb skills. Here we show that a third of new dendritic spines (postsynaptic structures of most excitatory synapses) formed during the acquisition phase of learning emerge in clusters, and the majority of such clusters are neighboring spine pairs. These clustered new spines are more likely to persist throughout prolonged learning sessions and even long after training stops, compared to non-clustered counterparts. Moreover, formation of new spine clusters requires repetition of the same motor task, and the emergence of succedent new spine(s) accompanies the strengthening of the first new spine in the cluster. We also show that under control conditions new spines appear to avoid existing stable spines, rather than being uniformly added along dendrites. However, succedent new spines in clusters overcome such a spatial constraint and form in close vicinity to neighboring stable spines. Our findings suggest that clustering of new synapses along dendrites is induced by repetitive activation of the cortical circuitry during learning, providing a structural basis for spatial coding of motor memory in the mammalian brain. 2012-02-19 /pmc/articles/PMC3292711/ /pubmed/22343892 http://dx.doi.org/10.1038/nature10844 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Fu, Min
Yu, Xinzhu
Lu, Ju
Zuo, Yi
REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO
title REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO
title_full REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO
title_fullStr REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO
title_full_unstemmed REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO
title_short REPETITIVE MOTOR LEARNING INDUCES COORDINATED FORMATION OF CLUSTERED DENDRITIC SPINES IN VIVO
title_sort repetitive motor learning induces coordinated formation of clustered dendritic spines in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3292711/
https://www.ncbi.nlm.nih.gov/pubmed/22343892
http://dx.doi.org/10.1038/nature10844
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