Experience-dependent development of perineuronal nets and chondroitin sulfate proteoglycan receptors in mouse visual cortex
Abstract
Perineuronal nets (PNNs) are extracellular matrix structures consisting of chondroitin sulfate proteoglycans (CSPGs), hyaluronan, link proteins and tenascin-R (Tn-R). They enwrap a subset of GABAergic inhibitory interneurons in the cerebral cortex and restrict experience-dependent cortical plasticity. While the expression profile of PNN components has been widely studied in many areas of the central nervous system of various animal species, it remains unclear how these components are expressed during the postnatal development of mouse primary visual cortex (V1). In the present study, we characterized the developmental time course of the formation of PNNs in the mouse primary visual cortex, using the specific antibodies against the two PNN component proteins aggrecan and tenascin-R, or the lectin Wisteria floribunda agglutinin (WFA) that directly binds to glycosaminoglycan chains of chondroitin sulfate proteoglycans (CSPGs). We found that the fluorescence staining signals of both the WFA staining and the antibody against aggrecan rapidly increased in cortical neurons across layers 2-6 during postnatal days (PD) 10-28 and reached a plateau around PD42, suggesting a full construction of PNNs by the end of the critical period. Co-staining with antibodies to Ca(2+) binding protein parvalbumin (PV) demonstrated that the majority of PNN-surrounding cortical neurons are immunoreactive to PV. Similar expression profile of another PNN component tenascin-R was observed in the development of V1. Dark rearing of mice from birth significantly reduced the density of PNN-surrounding neurons. In addition, the expression of two recently identified CSPG receptors - Nogo receptor (NgR) and leukocyte common antigen-related phosphatase (LAR), showed significant increases from PD14 to PD70 in layer 2-6 of cortical PV-positive interneurons in normal reared mice, but decreased significantly in dark-reared ones. Taken together, these results suggest that PNNs form preferentially in cortical PV-positive interneurons in an experience-dependent manner, and reach full maturation around the end of the critical period of V1 development.
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CSPG-enriched PNNs form in an activity-dependent manner during late postnatal development, completing neuronal maturation.
“CSPG-enriched PNNs form in an activity-dependent manner during late postnatal development, completing neuronal maturation.32, 33, 34”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [34]
Neuronal activity in sensory cortices during closure of a critical period is associated with both maturation of parvalbumin neurons and appearance of perineuronal nets.
“Consistent with this interpretation, neuronal activity in sensory cortices during the closure of a critical period is associated with both the maturation of PV neurons and the appearance of PNNs (Nowicka et al, 2009;Ye and Miao, 2013).”
From Reduced Labeling of Parvalbumin Neurons and Perineuronal Nets in the Dorsolateral Prefrontal Cortex of Subjects with Schizophrenia (2016) · cites this paper as Ye and Miao, 2013
NgR is present in PNN-encapsulated neurons and binds CSPGs.
“Finally, Nogo receptor (NgR), which binds myelin-associated proteins that inhibit axonal growth, such as the Nogo proteins, is expressed in PNN-encapsulated neurons (Ye and Miao, 2013) and also binds CSPGs (Dickendesher et al., 2012).”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Ye and Miao, 2013
In the mouse cortical V1 region, 82% of all VVA+ cells were found to also express PV.
“Similar numbers were reported in the mouse cortical V1 region, where 82 % of all VVA+ cells were found to also express PV [87].”
The maturation of PNNs in the developing cortex coincides with the closure of the critical periods of synaptogenesis and circuit refinement.
“The maturation of PNNs in the developing cortex coincides with the closure of the critical periods of synaptogenesis and circuit refinement (Beurdeley et al., 2012; Ye and Miao, 2013).”
From Adult neurogenesis, glia, and the extracellular matrix (2019) · cites this paper as Ye and Miao, 2013
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References 58 · Cited by 146
- Authors
- Ye, Q., & Miao, Q.-L.
- Affiliations
- Shanghai Jiao Tong University (CN)
- ORCID
- Ye, Qian
- Venue
- Matrix Biology
- Publisher
- Elsevier BV
- Published
- 2013-08
- Volume
- 32
- Issue
- 6
- Pages
- 352-363
- ISSN
- 0945-053X (ISSN-L)
- OpenAlex
- W2065527300
- Cited by
- 146
- References
- 58
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 16 · 2023: 13 · 2022: 7 · 2021: 10 · 2020: 13 · 2019: 16 · 2018: 13 · 2017: 14 · 2016: 12 · 2015: 9 · 2014: 8 · 2013: 1
- FWCI
- 5.80
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Matrix Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- 973 Program (2011CBA00403)
- 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
- perineuronal nets, chondroitin sulfate proteoglycans, primary visual cortex, postnatal development, experience-dependent plasticity, critical period, parvalbumin interneurons, tenascin-R, aggrecan, Nogo receptor, LAR, dark rearing, extracellular matrix, Wisteria floribunda agglutinin
- MeSH terms
- Nogo Proteins, Proteoglycan Link Protein, Animals, Animals, Newborn, Darkness, Extracellular Matrix, Female, Hyaluronic Acid, Immunohistochemistry, Male, Mice, Inbred C57BL, Myelin Proteins, Neurons, Parvalbumins, Chondroitin Sulfate Proteoglycans, Proteoglycans, Visual Cortex, Signal Transduction, Extracellular Matrix Proteins, Gene Expression Regulation, Developmental, Tenascin, Receptors, N-Acetylglucosamine, Plant Lectins, Mice, Aggrecans, Receptor-Like Protein Tyrosine Phosphatases, Class 2, Neurogenesis
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