Cited by 117Neuroscience and Neuropharmacology ResearchMitochondrial Function and PathologyGenetics and Neurodevelopmental Disorders

WAVE1 controls neuronal activity-induced mitochondrial distribution in dendritic spines

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Sung, Jee Young, Engmann, Olivia, Teylan, Merilee A., Nairn, Angus C., Greengard, Paul, Kim, Yong·2008·Proceedings of the National Academy of Sciences

Abstract

Mitochondrial fission and trafficking to dendritic protrusions have been implicated in dendritic spine development. Here, we show that Wiskott–Aldrich syndrome protein (WASP)-family verprolin homologous protein 1 (WAVE1) controls depolarization-induced mitochondrial movement into dendritic spines and filopodia and regulates spine morphogenesis. Depolarization-induced degradation of the p35 regulatory subunit of cyclin-dependent kinase 5 (Cdk5), with the resultant decreased inhibitory phosphorylation on WAVE1, depend on NMDA receptor activation. Thus, WAVE1 dephosphorylation and activation are likely associated with mitochondrial redistribution and spine morphogenesis.

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Crossref · 10.1073/pnas.0712180105

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  • In primary cultured neurons, WAVE1-mediated actin polymerization is involved in neuronal activity-induced mitochondrial trafficking and fission.

    “In primary cultured neurons, WAVE1-mediated actin polymerization is involved in neuronal activity-induced mitochondrial trafficking and fission45 (Fig. 4a).”

    From The WAVE complex in developmental and adulthood brain disorders (2025) · cites this paper as [45]

    The Results and Discussion support a role for WAVE1 in activity-induced mitochondrial trafficking to dendritic protrusions in cultured neurons. The Discussion describes mediation by WAVE1-dependent actin polymerization as likely, not established, and says depolarization-induced fission still occurred when WAVE1 expression was reduced. Page numbers are not available in our copy. (LLM, conf=0.90)

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  • In primary cultured cortical neurons, repetitive depolarization by KCl induces WAVE1 dephosphorylation in an NMDA receptor-dependent manner.

    “In primary cultured cortical neurons, repetitive depolarization by KCl induces WAVE1 dephosphorylation in an NMDA receptor-dependent manner45.”

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Authors
Sung, J. Y., Engmann, O., Teylan, M. A., Nairn, A. C., Greengard, P., & Kim, Y.
Affiliations
  • Rockefeller University (US)
  • Yale University (US)
Venue
Proceedings of the National Academy of Sciences
Published
2008-02-26
Volume
105
Issue
8
Pages
3112-3116
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2163296768
Cited by
117
References
4
Citations by year
2026: 7 · 2025: 2 · 2024: 5 · 2023: 3 · 2022: 5 · 2021: 1 · 2020: 8 · 2019: 4 · 2018: 5 · 2017: 7 · 2016: 10 · 2015: 5 · 2014: 7 · 2013: 5 · 2012: 9
FWCI
4.66
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • F. M. Kirby Foundation
  • Fisher Center for Alzheimer's Research Foundation
  • James N. Kirby Foundation
  • National Institute on Aging (AG09464, P01AG009464)
  • National Institute on Drug Abuse (DA10044, P01DA010044)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
Keywords
WAVE1, dendritic spines, mitochondrial trafficking, mitochondrial fission, neuronal depolarization, filopodia, spine morphogenesis, NMDA receptor, Wiskott-Aldrich syndrome protein, neuronal activity, dendritic protrusions
MeSH terms
Animals, Hippocampus, Image Processing, Computer-Assisted, Microscopy, Fluorescence, Mitochondria, Phosphorylation, Receptors, N-Methyl-D-Aspartate, Rats, Sprague-Dawley, RNA Interference, Dendritic Spines, Wiskott-Aldrich Syndrome Protein Family, Rats

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