Diverse Roles of Rho Family GTPases in Neuronal Development, Survival, and Death
Open accessAbstract
Rho family GTPases (eg., RhoA, Rac1 and Cdc42) are monomeric G-proteins that act as key transducers of extracellular signals to the actin cytoskeleton. In the nervous system, Rho family GTPases are essential regulators of neuronal growth cone motility, axonal migration, and dendritic spine morphogenesis. Given these vital functions, it is perhaps not surprising that mutations in several proteins involved in Rho GTPase signaling are causative in some forms of mental retardation. In addition, numerous recent studies have identified Rho family GTPases as central players in the molecular pathways that determine neuronal survival and death. Interestingly, individual Rho family members have been shown to play either a pro-death or pro-survival role in the nervous system depending on both the type of neuron and the particular neurodegenerative insult involved. This review summarizes current work demonstrating a critical role for Rho family GTPases and their effectors in the regulation of neuronal development, survival, and death. These findings may be particularly relevant in the context of specific neurodegenerative disorders in which Rho family GTPase function is altered, such as loss-of-function of the Rac1 guanine nucleotide exchange factor, alsin, in juvenile-onset amyotrophic lateral sclerosis.
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RhoA activity has been related to developmental disabilities, such as mental retardation.
“Therefore, it is not surprising that RhoA activity has been related to developmental disabilities, such as mental retardation [55].”
From Brain Cholesterol Biosynthetic Pathway Is Altered in a Preclinical Model of Fragile X Syndrome (2022) · cites this paper as [55]
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References 168 · Cited by 134
Research works printed but not linked: 2
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- Authors
- Linseman, D.
- Venue
- Frontiers in Bioscience
- Publisher
- IMR Press
- Published
- 2008
- Volume
- 13
- Issue
- 13
- Pages
- 657
- ISSN
- 1093-4715 (ISSN-L)
- 1093-9946
- DOI
- 10.2741/2710
- OpenAlex
- W66461172
- Cited by
- 134
- References
- 168
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 1 · 2023: 3 · 2022: 3 · 2021: 1 · 2020: 4 · 2019: 3 · 2018: 9 · 2017: 3 · 2016: 8 · 2015: 12 · 2014: 10 · 2013: 14 · 2012: 13
- FWCI
- 0.90
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Frontiers in bioscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs
- 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
- Rho GTPases, RhoA, Rac1, Cdc42, neuronal development, neuronal survival, neuronal cell death, actin cytoskeleton, growth cone motility, dendritic spine morphogenesis, intellectual disability, neurodegenerative diseases, alsin, amyotrophic lateral sclerosis, guanine nucleotide exchange factor
- MeSH terms
- Amyotrophic Lateral Sclerosis, Animals, Cell Survival, Fragile X Syndrome, Gene Expression Regulation, Humans, Models, Biological, Motor Neurons, Neurons, Tuberous Sclerosis, rho GTP-Binding Proteins, cdc42 GTP-Binding Protein, X-Linked Intellectual Disability, Mental Retardation, X-Linked, Dendritic Spines, p21-Activated Kinases
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