Transsynaptic Signaling of Ephs in Synaptic Development, Plasticity, and Disease
Open accessAbstract
Synapse formation between neurons is critical for proper circuit and brain function. Prior to activity-dependent refinement of connections between neurons, activity-independent cues regulate the contact and recognition of potential synaptic partners. Formation of a synapse results in molecular recognition events that initiate the process of synaptogenesis. Synaptogenesis requires contact between axon and dendrite, selection of correct and rejection of incorrect partners, and recruitment of appropriate pre- and postsynaptic proteins needed for the establishment of functional synaptic contact. Key regulators of these events are families of transsynaptic proteins, where one protein is found on the presynaptic neuron and the other is found on the postsynaptic neuron. Of these families, the EphBs and ephrin-Bs are required during each phase of synaptic development from target selection, recruitment of synaptic proteins, and formation of spines to regulation of synaptic plasticity at glutamatergic spine synapses in the mature brain. These roles also place EphBs and ephrin-Bs as important regulators of human neurological diseases. This review will focus on the role of EphBs and ephrin-Bs at synapses.
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Proteins regulated by chr3q28 region included five members of the syntaxin family and five ephrin family members.
“Proteins regulated by this region included five members of the syntaxin family involved in synapse function31 and five ephrin family members involved in neural development and memory32,33.”
From Proteogenomic analysis of human cerebrospinal fluid identifies neurologically relevant regulation and implicates causal proteins for Alzheimer’s disease (2024) · cites this paper as [33]
Cites
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Western, D., Timsina, J., Wang, L., Wang, C., Yang, C., Phillips, B., Wang, Y., Liu, M., Ali, M., Beric, A., et al. (2024) · Nature Genetics · doi:10.1038/s41588-024-01972-8 · Cited by 111 · see citing works
- Authors
- Washburn, H. R., Chander, P., Srikanth, K. D., & Dalva, M. B.
- Affiliations
- Thomas Jefferson University (US)
- Corresponding author
- Dalva, Matthew B.
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2023-01
- Volume
- 508
- Pages
- 137-152
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W4311983083
- Cited by
- 13
- References
- 3
- Citations by year
- 2026: 1 · 2025: 7 · 2024: 4 · 2023: 1
- FWCI
- 0.43
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuroscience (acceptedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute on Drug Abuse (R01DA022727)
- National Institute of Neurological Disorders and Stroke (R01NS106906, R01NS111976, R01NS110385)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- EphB receptors, trans-synaptic signaling, synaptogenesis, synaptic development, synaptic plasticity, synaptic pruning, dendritic spine formation, glutamatergic synapses, neurological disorders
- MeSH terms
- Axons, Cell Communication, Humans, Neuronal Plasticity, Neurons, Synapses, Ephrins
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