Cited by 56Axon Guidance and Neuronal SignalingCellular Mechanics and InteractionsNeurogenesis and neuroplasticity mechanisms

Controlling actin cytoskeletal organization and dynamics during neuronal morphogenesis

Kessels, Michael Manfred, Schwintzer, Lukas, Schlobinski, Dirk, Qualmann, Britta·2011·European Journal of Cell Biology

Abstract

Coordinated functions of the actin cytoskeleton and microtubules, which need to be carefully controlled in time and space, are required for the drastic alterations of neuronal morphology during neuromorphogenesis and neuronal network formation. A key process in neuronal actin dynamics is filament formation by actin nucleators, such as the Arp2/3 complex, formins and the brain-enriched, novel WH2 domain-based nucleators Spire and cordon-bleu (Cobl). We here discuss in detail the currently available data on the roles of these actin nucleators during neuromorphogenesis and highlight how their required control at the plasma membrane may be brought about. The Arp2/3 complex was found to be especially important for proper growth cone translocation and axon development. The underlying molecular mechanisms for Arp2/3 complex activation at the neuronal plasma membrane include a recruitment and an activation of N-WASP by lipid- and F-actin-binding adaptor proteins, Cdc42 and phosphatidyl-inositol-(4,5)-bisphosphate (PIP(2)). Together, these components upstream of N-WASP and the Arp2/3 complex ensure fine-control of N-WASP-mediated Arp2/3 complex activation and control distinct functions during axon development. They are counteracted by Arp2/3 complex inhibitors, such as PICK, which likewise play an important role in neuromorphogenesis. In contrast to the crucial role of the Arp2/3 complex in proper axon development, dendrite formation and dendritic arborization was revealed to critical…

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Crossref · 10.1016/j.ejcb.2010.08.011

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  • Rapid polymerization and depolymerization of actin filaments produces protrusive forces that can quickly change neuronal morphology.

    “The rapid polymerization and depolymerization of actin filaments produces protrusive forces that can quickly change neuronal morphology (Kessels et al., 2011).”

    From Barriers in the brain: resolving dendritic spine morphology and compartmentalization (2014) · cites this paper as Kessels et al., 2011

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Authors
Kessels, M. M., Schwintzer, L., Schlobinski, D., & Qualmann, B.
Affiliations
Jena University Hospital (DE)
Corresponding author
  • Kessels, Michael Manfred
  • Qualmann, Britta
Venue
European Journal of Cell Biology
Publisher
Elsevier BV
Published
2011-11
Volume
90
Issue
11
Pages
926-933
ISSN
0171-9335 (ISSN-L)
OpenAlex
W1974768054
Cited by
56
References
0
Citations by year
2026: 3 · 2025: 2 · 2024: 3 · 2022: 4 · 2021: 6 · 2020: 4 · 2019: 3 · 2018: 2 · 2017: 1 · 2016: 2 · 2015: 3 · 2014: 4 · 2013: 8 · 2012: 5
FWCI
0.55
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of Cell Biology (publishedVersion)
  • PubMed (publishedVersion)
Funders
Deutsche Forschungsgemeinschaft
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords
actin cytoskeleton, neuronal morphogenesis, actin nucleators, Arp2/3 complex, formins, spire, cordon bleu, N-WASP, Cdc42, phosphatidylinositol 4,5-bisphosphate, picks, dendrite formation, dendritic branching, axon development, growth cones, WH2 domain, actin dynamics
MeSH terms
Animals, Biological Transport, Humans, Actin Cytoskeleton, Microtubules, Neurons, Neurogenesis

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