Regulation of neural circuit formation by protocadherins
Open accessAbstract
The protocadherins (Pcdhs), which make up the most diverse group within the cadherin superfamily, were first discovered in the early 1990s. Data implicating the Pcdhs, including ~60 proteins encoded by the tandem Pcdha, Pcdhb, and Pcdhg gene clusters and another ~10 non-clustered Pcdhs, in the regulation of neural development have continually accumulated, with a significant expansion of the field over the past decade. Here, we review the many roles played by clustered and non-clustered Pcdhs in multiple steps important for the formation and function of neural circuits, including dendrite arborization, axon outgrowth and targeting, synaptogenesis, and synapse elimination. We further discuss studies implicating mutation or epigenetic dysregulation of Pcdh genes in a variety of human neurodevelopmental and neurological disorders. With recent structural modeling of Pcdh proteins, the prospects for uncovering molecular mechanisms of Pcdh extracellular and intracellular interactions, and their role in normal and disrupted neural circuit formation, are bright.
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β-Protocadherins are upregulated in all astrocytes by aging.
“β-Protocadherins are upregulated in all astrocytes by aging, and although little is known about their function, the related γ-protocadherins have important roles in developmental synapse formation (Peek et al., 2017).”
From The aging astrocyte transcriptome from multiple regions of the mouse brain. (2018) · cites this paper as Peek et al., 2017
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References 210 · Cited by 119
Research works printed but not linked: 1
- [200]Nemeroff CC 2004 Early-Life Adversity, CRF Dysregulation, and Vulnerability to Mood and Anxiety Disorders Psychopharmacology bulletin 38 1 14 20 15278013
- Authors
- Peek, S. L., Mah, K. M., & Weiner, J. A.
- Affiliations
- University of Iowa (US)
- Corresponding author
- Weiner, Joshua A.
- Venue
- Cellular and Molecular Life Sciences
- Published
- 2017-06-19
- Volume
- 74
- Issue
- 22
- Pages
- 4133-4157
- ISSN
- 1420-682X (ISSN-L)
- 1420-9071
- PMC
- PMC5643215
- OpenAlex
- W2652717092
- Cited by
- 119
- References
- 210
- Citations by year
- 2026: 10 · 2025: 11 · 2024: 17 · 2023: 17 · 2022: 13 · 2021: 19 · 2020: 15 · 2019: 12 · 2018: 3 · 2017: 2
- FWCI
- 1.08
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Cellular and Molecular Life Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01 NS055272, R21 NS090030)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- protocadherins, neural circuit formation, neural development, dendritic branching, axon growth, axon targeting, synaptogenesis, synaptic pruning, neurodevelopmental disorders, neurological disorders, epigenetic dysregulation, cadherin superfamily, protein structure modeling
- MeSH terms
- Animals, Axons, Dendrites, Humans, Nervous System Diseases, Neurons, Synapses, Signal Transduction, Cadherins
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