Cited by 296Neuroscience and Neuropharmacology ResearchMemory and Neural MechanismsGenetics and Neurodevelopmental Disorders

Changes in Synaptic Morphology Accompany Actin Signaling during LTP

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Chen, Lulu Y., Rex, Christopher S., Casale, Malcolm S., Gall, Christine M., Lynch, Gary·2007·The Journal of Neuroscience

Abstract

Stabilization of long-term potentiation (LTP) is commonly proposed to involve changes in synaptic morphology and reorganization of the spine cytoskeleton. Here we tested whether, as predicted from this hypothesis, induction of LTP by theta-burst stimulation activates an actin regulatory pathway and alters synapse morphology within the same dendritic spines. TBS increased severalfold the numbers of spines containing phosphorylated (p) p21-activated kinase (PAK) or its downstream target cofilin; the latter regulates actin filament assembly. The PAK/cofilin phosphoproteins were increased at 2 min but not 30 s post-TBS, peaked at 7 min, and then declined. Double immunostaining for the postsynaptic density protein PSD95 revealed that spines with high pPAK or pCofilin levels had larger synapses (+60–70%) with a more normal size frequency distribution than did neighboring spines. Based on these results and simulations of shape changes to synapse-like objects, we propose that theta stimulation markedly increases the probability that a spine will enter a state characterized by a large, ovoid synapse and that this morphology is important for expression and later stabilization of LTP.

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Crossref · 10.1523/jneurosci.0164-07.2007

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References 60 · Cited by 296

Research works printed but not linked: 2

  1. Jain AK (1984) Fundamentals of digital image processing. Englewood Cliffs, NJ: Prentice Hall.
  2. Nagerl UV, Eberhorn N, Cambridge SB, Bonhoeffer T (2004) Bidirectional activity-dependent morphological plasticity in hippocampal neurons. Neuron 44:759 -767.

Authors
Chen, L. Y., Rex, C. S., Casale, M. S., Gall, C. M., & Lynch, G.
Affiliations
University of California, Irvine (US)
Corresponding author
Gall, Christine M.
Venue
The Journal of Neuroscience
Published
2007-05-16
Volume
27
Issue
20
Pages
5363-5372
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2000508605
Cited by
296
References
60
Citations by year
2026: 4 · 2025: 5 · 2024: 9 · 2023: 11 · 2022: 8 · 2021: 9 · 2020: 13 · 2019: 14 · 2018: 9 · 2017: 18 · 2016: 24 · 2015: 20 · 2014: 27 · 2013: 14 · 2012: 21
FWCI
9.69
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • eScholarship (California Digital Library) (submittedVersion)
Funders
  • University of California, Irvine
  • National Institute on Aging (AG00358)
  • National Institute of Neurological Disorders and Stroke (P01NS045260, NS 37799, NS051823, NS-45260, R01NS037799, R01NS051823)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
Keywords
long-term potentiation, synaptic morphology, dendritic spines, actin cytoskeleton, p21-activated kinase, cofilin, theta burst stimulation, PSD-95, synapse size
MeSH terms
Actins, Animals, Male, Synapses, Time Factors, Signal Transduction, Rats, Sprague-Dawley, Long-Term Potentiation, Dendritic Spines, Rats

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