Cited by 25Neuroscience and Neuropharmacology ResearchGenetics and Neurodevelopmental DisordersProtein Kinase Regulation and GTPase Signaling

The RhoA-associated protein Citron-N controls dendritic spine maintenance by interacting with spine-associated Golgi compartments

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Camera, Paola, Schubert, Vanessa, Pellegrino, Maurizio, Berto, Gaia, Vercelli, Alessandro, Muzzi, Patrizia, Hirsch, Emilio, Altruda, Fiorella +2 more·2008·The EMBO Reports

Abstract

Dendritic spines are highly dynamic protuberances that are thought to be crucial for learning and memory. Although it is well known that actin filaments and membrane dynamics regulate spine plasticity, how these two events are linked locally is less clear. Here, we provide evidence that Citron-N (CIT-N), a binding partner of the small GTPase RhoA, is associated with the actin filaments and Golgi compartments of dendritic spines. We also show that CIT-N is required for recruiting F-actin and Golgi membranes at spines of in vitro-grown neurons. Studies in knockout mice show that this protein is essential for the maturation of dendritic spines. We suggest that CIT-N might function as a scaffold protein in spine organization through its ability to bind to Golgi membranes and by affecting actin remodelling.

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Crossref · 10.1038/embor.2008.21

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  • Citron N maintains Golgi architecture by modulating local actin polymerization together with ROCK.

    “Citron N is enriched in dendritic spines and is associated with the endomembrane system, in particular the Golgi complex, where it maintains Golgi architecture by modulating local actin polymerization together with ROCK [126,127].”

    From RhoA Signaling in Neurodegenerative Diseases (2022) · cites this paper as [127]

  • Citron N is enriched in dendritic spines and is associated with the endomembrane system, in particular the Golgi complex.

    “Citron N is enriched in dendritic spines and is associated with the endomembrane system, in particular the Golgi complex, where it maintains Golgi architecture by modulating local actin polymerization together with ROCK [126,127].”

    From RhoA Signaling in Neurodegenerative Diseases (2022) · cites this paper as [127]

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Research works printed but not linked: 1

  1. Goslin K, Banker GA (1991) Culturing Nerve Cells, pp 251-281. Cambridge, MA, USA: MIT Press

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Authors
Camera, P., Schubert, V., Pellegrino, M., Berto, G., Vercelli, A., Muzzi, P., Hirsch, E., Altruda, F., Dotti, C. G., & Di Cunto, F.
Affiliations
  • University of Turin (IT)
  • Ospedale San Luigi Gonzaga (IT)
Venue
The EMBO Reports
Published
2008-02-29
Volume
9
Issue
4
Pages
384-392
ISSN
  • 1469-221X (ISSN-L)
  • 1469-3178
OpenAlex
W2102312146
Cited by
25
References
1
Citations by year
2026: 4 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 1 · 2019: 2 · 2018: 3 · 2017: 1 · 2014: 3 · 2013: 2
FWCI
0.55
Type
journal article
Language
en
Open access
Locations
  • EMBO Reports (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Institutional Research Information System University of Turin (University of Turin) (submittedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
Keywords
RhoA, dendritic spines, F-actin, Golgi membranes, spine maturation, actin cytoskeleton remodeling, scaffold proteins, spine plasticity, learning and memory
MeSH terms
Actins, Animals, Cells, Cultured, Golgi Apparatus, Microscopy, Fluorescence, Neurons, Immunoblotting, Protein Serine-Threonine Kinases, Immunoprecipitation, Intracellular Signaling Peptides and Proteins, Dendritic Spines, Rats

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