Cited by 44Proteoglycans and glycosaminoglycans researchNeurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology Research

Chondroitin sulfate proteoglycans in neural development and plasticity

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Maeda, Nobuaki·2010·Frontiers in Bioscience

Abstract

PTPzeta and lectican family members are major chondroitin sulfate proteoglycans (CS-PGs) in the brain, which bind with many proteins via core protein and CS portions. Recent studies revealed that the oversulfated structures in CS constitute high affinity binding sites for various growth factors and axon guidance molecules, and play important roles in the proliferation of neural progenitor cells, neurite extension and neuronal migration. PTPzeta uses pleiotrophin as a ligand. The CS portion of PTPzeta constitutes a part of the pleiotrophin-binding site, and oversulfated D unit increases the binding affinity. Pleiotrophin-PTPzeta signaling regulates the morphogenesis of Purkinje cell by controlling the tyrosine phosphorylation of a Notch-related transmembrane protein, DNER. In the brain of adult animals, a subset of neurons are surrounded by CS-PG-rich extracellular matrix called perineuronal net, in which lecticans form complexes with hyaluronic acid and tenascin-R. CS-PGs in the perineuronal net regulate ocular dominance plasticity in the visual cortex by enhancing the uptake of Otx2 homeoprotein by parvalbumin-positive interneurons in a CS-dependent manner. These studies revealed unexpectedly complex mechanisms of CS-PG functions.

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  • Once formed, PNNs control neuronal access to growth and transcription factors, stabilize synaptic connectivity and compartmentalize the neuronal surface, regulating availability of glutamatergic receptors and neuronal firing properties.

    “Once formed, and throughout adulthood, PNNs control neuronal access to growth and transcription factors, stabilize synaptic connectivity and compartmentalize the neuronal surface, regulating the availability of glutamatergic receptors to postsynaptic specializations and, thus, neuronal firing properties.23, 25, 38”
  • PNN maturation occurs in an experience-dependent manner, requiring neuronal activation through glutamatergic excitation, availability of key PNN components, expression on neurons of ECM surface receptors, and transcription factors inducing neuronal maturation.

    “Their maturation occurs in an experience-dependent manner, requiring (i) neuronal activation through glutamatergic excitation,78 (ii) availability of key PNN components, such as specific CSPGs, link proteins and tenascin R, (iii) expression on neurons of ECM surface receptors79, 80 and (iv) transcription factors inducing neuronal maturation.25, 38”

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References 75 · Cited by 44

Authors
Maeda, N.
Corresponding author
Maeda, Nobuaki
Venue
Frontiers in Bioscience
Publisher
IMR Press
Published
2010
Volume
15
Issue
1
Pages
626
ISSN
  • 1093-4715 (ISSN-L)
  • 1093-9946
OpenAlex
W2025557177
Cited by
44
References
75
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 2 · 2022: 3 · 2021: 4 · 2020: 2 · 2019: 2 · 2018: 2 · 2017: 1 · 2016: 3 · 2015: 3 · 2014: 1 · 2013: 5 · 2012: 4
FWCI
0.30
Type
journal article
Language
en
Open access
Locations
  • Frontiers in bioscience (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Naito Foundation
  • Japan Society for the Promotion of Science (22570149)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords
chondroitin sulfate proteoglycans, lecticans, neural development, neuroplasticity, pleiotrophin, DNER, Notch signaling, perineuronal nets, ocular dominance plasticity, Otx2, parvalbumin interneurons, hyaluronic acid, tenascin-R, neural progenitor proliferation, neurite outgrowth, neuronal migration, growth factor binding
MeSH terms
Animals, Humans, Models, Biological, Neuronal Plasticity, Neurons, Chondroitin Sulfate Proteoglycans, Molecular Structure, Neurites, Cell Proliferation, Neurogenesis

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