Cdc42: an important regulator of neuronal morphology
Abstract
Regulation of neuronal morphology and activity-dependent synaptic modifications involves reorganization of the actin cytoskeleton. Dynamic changes of the actin cytoskeleton in many cell types are controlled by small GTPases of the Rho family, such as RhoA, Rac1 and Cdc42. As key regulators of both actin and microtubule cytoskeleton, Rho GTPases have also emerged as important regulators of dendrite and spine structural plasticity. Multiple studies suggest that Rac1 and Cdc42 are positive regulators promoting neurite outgrowth and growth cone protrusion, while the activation of RhoA induces stress fiber formation, leading to growth cone collapse and neurite retraction. This review focuses on recent advances in our understanding of the molecular mechanisms underlying physiological and pathological functions of Cdc42 in the nervous system. We also discuss application of different FRET-based biosensors as a powerful approach to examine the dynamics of Cdc42 activity in living cells.
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Upregulation of SGK1 elevates levels of actin remodeling-related proteins Rictor, Rac1, Cdc42, and Profilin-1 in the hippocampus of AD mice, which may impact neuronal structure and function.
“Furthermore, upregulation of SGK1 elevates the levels of actin remodeling-related proteins, such as Rictor, Rac1, Cdc42, and Profilin-1 in the hippocampus of AD mice, which may impact the structure and function of neurons”
From Serum/glucocorticoid regulated kinase 1 (SGK1) in neurological disorders: pain or gain (2024) · cites this paper as Chen et al., 2012
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Local, persistent activation of Rho GTPases during plasticity of single dendritic spines
Murakoshi, H., Wang, H., & Yasuda, R. (2011) · Nature · doi:10.1038/nature09823 · Cited by 564 · see citing works
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Serum/glucocorticoid regulated kinase 1 (SGK1) in neurological disorders: pain or gain
Howard, P. G., Zou, P., Zhang, Y., Huang, F., Tesic, V., Wu, C. Y.-C., & Lee, R. H.-C. (2024) · Experimental Neurology · doi:10.1016/j.expneurol.2024.114973 · Cited by 13 · see citing works
- Authors
- Chen, C., Wirth, A., & Ponimaskin, E.
- Affiliations
- Medizinische Hochschule Hannover (DE)
- Corresponding author
- Ponimaskin, Evgeni
- Venue
- The International Journal of Biochemistry & Cell Biology
- Publisher
- Elsevier BV
- Published
- 2012-03
- Volume
- 44
- Issue
- 3
- Pages
- 447-451
- ISSN
- 1357-2725 (ISSN-L)
- OpenAlex
- W2087147111
- Cited by
- 72
- References
- 1
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 7 · 2023: 2 · 2022: 9 · 2021: 6 · 2020: 3 · 2018: 5 · 2017: 3 · 2016: 7 · 2015: 5 · 2014: 6 · 2013: 8 · 2012: 3
- FWCI
- 0.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The International Journal of Biochemistry & Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- Cdc42, Rho GTPases, neuronal morphology, actin cytoskeleton, dendritic spine plasticity, neurite outgrowth, growth cones, RhoA, Rac1, FRET biosensor, synaptic plasticity, microtubule cytoskeleton
- MeSH terms
- Animals, Humans, Actin Cytoskeleton, Nerve Growth Factors, Neurons, Sensory Receptor Cells, Signal Transduction, Monomeric GTP-Binding Proteins, cdc42 GTP-Binding Protein, Memory, Long-Term
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